KITS FOR ANALYSIS USING NUCLEIC ACID CODING AND / OR LABELING

Abstract

Kits and methods of using the kits for analyzing macromolecules, including peptides, polypeptides, and proteins, employing nucleic acid encoding are disclosed. The sample analysis kits employ nucleic acid encoding and / or nucleic acid recording of a molecular interaction and / or reaction, such as recognition events (e.g., between an antigen and an antibody, between a modified terminal amino acid residue, or between a small molecule or peptide therapeutic and a target, etc.). Additional barcoding reagents, such as those for cycle-specific barcoding (e.g., "clocking"), compartment barcoding, combinatorial barcoding, spatial barcoding, or any combination thereof, may be included in the kits. The sample may comprise macromolecules, including peptides, polypeptides, and proteins, and the recording may generate molecular interaction and / or reaction information, and / or polypeptide sequence information. The kits may be used in high-throughput, multiplexed, and / or automated analysis, and are suitable for analysis of a proteome or subset thereof.

Description

KITS FOR ANALYSIS USING NUCLEIC ACID ENCODING AND / OR LABELCross-Reference to Related Applications

[0001] This application claims benefit of priority to U.S. Provisional Application Serial No. 62 / 579,844, filed 31 October 2017, entitled "KITS FOR ANALYSIS USING NUCLEIC ACID ENCODING AND / OR LABEL," and to U.S. Provisional Application Serial No. 62 / 582,312, filed 6 November 2017, entitled "KITS FOR ANALYSIS USING NUCLEIC ACID ENCODINGAND / OR LABEL," and to U.S. Provisional Application Serial No. 62 / 583,448, filed 8 November 2017, entitled "KITS FOR ANALYSIS USING NUCLEIC ACID ENCODING AND / OR LABEL": the entire contents of each of these applications are incorporated herein by reference for all purposes. This application is related to U.S. Provisional Patent Application No. 62 / 330,841, filed May 2, 2016, entitled "Macromolecule Analysis Employing Nucleic Acid Encoding"; U.S.Provisional Patent Application No. 62 / 339,071, filed May 19, 2016, entitled "Macromolecule Analysis Employing Nucleic Acid Encoding"; U.S. Provisional Patent Application No. 62 / 376,886, filed August 18, 2016, entitled "Macromolecule Analysis Employing Nucleic Acid Encoding"; International Patent Application No. PCT / US2017 / 030702, filed May 2, 2017, entitled"Macromolecule Analysis Employing Nucleic Acid Encoding"; U.S. Provisional Patent Application No. 62 / 579,844, having the Attorney Docket No. 776533000500, filed October 31, 2017, entitled "Kits for Analysis Using Nucleic Acid Encoding and / or Label"; U.S. Provisional Patent Application No. 62 / 579,870, having the Attorney Docket No. 776533000600, filed October 31, 2017, entitled "Methods and Compositions for Polypeptide Analysis"; U.S. Provisional Patent Application No. 62 / 579,840, having the Attorney Docket No. 776533000700, filed October 31, 2017, entitled "Methods and Kits Using Nucleic Acid Encoding and / or Label"; U.S. Provisional PatentApplication No. 62 / 582,312, having the Attorney Docket No. 776533000501, filed November 6, 2017, entitled "Kits for Analysis Using Nucleic Acid Encoding and / or Label"; and U.S. Provisional Patent Application No. 62 / 582,916, having the Attorney Docket No. 776533000701, filedNovember 7, 2017, entitled "Methods and Kits Using Nucleic Acid Encoding and / or Label," the disclosures of which applications are incorporated herein by reference for all purposes.Submission of Sequence Listing on ASCII Text File

[0002] The content of the following submission on ASCII text file is incorporated herein by reference in its entirety: a computer readable form (CRF) of the Sequence Listing (file name: 4614- 2000540_20181031_SeqList.txt, date recorded: October 31, 2018, size: 52 Kbytes).Field

[0003] The present disclosure generally relates to sample analysis kits employing nucleic acid encoding and / or nucleic acid recording of a molecular interaction and / or reaction, such as recognition events. In some embodiments, the kits may be used in high-throughput, multiplexed, and / or automated analysis, and are suitable for analysis of a proteome or subset thereof.Background

[0004] Proteins play an integral role in cell biology and physiology, performing and facilitating many different biological functions. The repertoire of different protein molecules is extensive, much more complex than the transcriptome, due to additional diversity introduced by post- translational modifications (PTMs). Additionally, proteins within a cell dynamically change (in expression level and modification state) in response to the environment, physiological state, and disease state. Thus, proteins contain a vast amount of relevant information that is largely unexplored, especially relative to genomic information. In general, innovation has been lagging in proteomics analysis relative to genomics analysis. In the field of genomics, next-generation sequencing (NGS) has transformed the field by enabling analysis of billions of DNA sequences in a single instrument run, whereas in protein analysis and peptide sequencing, throughput is still limited.

[0005] Yet this protein information is direly needed for a better understanding of proteome dynamics in health and disease and to help enable precision medicine. As such, there is great interest in developing "next-generation" tools to miniaturize and highly-parallelize collection of this proteomic information. The present disclosure addresses these and other needs.Summary

[0006] The summary is not intended to be used to limit the scope of the claimed subject matter. Other features, details, utilities, and advantages of the claimed subject matter will be apparent from the detailed description including those aspects disclosed in the accompanying drawings and in the appended claims.

[0007] In any of the embodiments in this summary herein, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0008] In one aspect, disclosed herein is a kit, comprising: (a) a recording tag configured to associate directly or indirectly with an analyte; (b) (i) a coding tag which comprises identifying information regarding a binding moiety capable of binding to the analyte, and which is configured to associate directly or indirectly with the binding moiety to form a binding agent, and / or (ii) a label, wherein the recording tag and the coding tag are configured to allow transfer of information between them, upon binding between the binding agent and the analyte; and optionally (c) the binding moiety. In one embodiment, the recording tag and / or the analyte are configured to be immobilized directly or indirectly to a support. In a further embodiment, the recording tag is configured to be immobilized to the support, thereby immobilizing the analyte associated with the recording tag. In another embodiment, the analyte is configured to be immobilized to the support, thereby immobilizing the recording tag associated with the analyte. In yet another embodiment, each of the recording tag and the analyte is configured to be immobilized to the support. In still another embodiment, the recording tag and the analyte are configured to co-localize when both are immobilized to the support. In some embodiments, the distance between (i) an analyte and (ii) a recording tag for information transfer between the recording tag and the coding tag of a binding agent bound to the analyte, is less than about 10"6nm, about 10"6nm, about 10"5nm, about 10"4nm, about 0.001 nm, about 0.01 nm, about 0.1 nm, about 0.5 nm, about 1 nm, about 2 nm, about 5 nm, or more than about 5 nm, or of any value in between the above ranges.

[0009] In any of the preceding embodiments, the kit can further comprise an immobilizing linker configured to: (i) be immobilized directly or indirectly to a support, and (ii) associate directly or indirectly with the recording tag and / or the analyte. In one embodiment, the immobilizing linker is configured to associate with the recording tag and the analyte.

[0010] In any of the preceding embodiments, the immobilizing linker can be configured to be immobilized directly to the support, thereby immobilizing the recording tag and / or the analyte which are associated with the immobilizing linker.

[0011] In any of the preceding embodiments, the kit can further comprise the support.

[0012] In any of the preceding embodiments, the kit can further comprise one or more reagents for transferring information between the coding tag and the recording tag, upon binding between the binding agent and the analyte. In one embodiment, the one or more reagents are configured to transfer information from the coding tag to the recording tag, thereby generating an extended recording tag. In another embodiment, the one or more reagents are configured to transfer information from the recording tag to the coding tag, thereby generating an extended coding tag. In yet another embodiment, the one or more reagents are configured to generate a di-tag construct comprising information from the coding tag and information from the recording tag.

[0013] In any of the preceding embodiments, the kit can comprise at least two of the recording tags. In any of the preceding embodiments, the kit can comprise at least two of the coding tags each comprising identifying information regarding its associated binding moiety. In particular embodiments, each analyte has a plurality of recording tags (e.g., at least about two, about five, about ten, about 20, about 50, about 100, about 200, about 500, about 1000, about 2000, about 5000, or more) available to a binding agent bound to that analyte. In particular embodiments, the kit comprises a plurality of recording tags, e.g., at least about two, about five, about ten, about 20, about 50, about 100, about 200, about 500, about 1000, about 2000, about 5000, or more.

[0014] In any of the preceding embodiments, the kit can comprise at least two of the binding agents. In one embodiment, the kit comprises: (i) one or more reagents for transferring information from a first coding tag of a first binding agent to the recording tag to generate a first order extended recording tag, upon binding between the first binding agent and the analyte, and / or (ii) one or more reagents for transferring information from a second coding tag of a second binding agent to the firstorder extended recording tag to generate a second order extended recording tag, upon binding between the second binding agent and the analyte, wherein the one or more reagents of (i) and the one or more reagents of (ii) can be the same or different. In particular embodiments, each analyte has a plurality of binding agents and / or coding tags, e.g., at least about two, about five, about ten, about 20, about 50, about 100, about 200, about 500, about 1000, about 2000, about 5000, or more, available to a recording tag for the analyte, and the plurality of binding agents may be added sequentially or in parallel. In particular embodiments, the kit comprises a plurality of binding agents and / or coding tags, e.g., at least about two, about five, about ten, about 20, about 50, about 100, about 200, about 500, about 1000, about 2000, about 5000, or more.

[0015] In any of the preceding embodiments, the kit can further comprise (iii) one or more reagents for transferring information from a third (or higher order) coding tag of a third (or higher order) binding agent to the second order extended recording tag to generate a third (or higher order) order extended recording tag, upon binding between the third (or higher order) binding agent and the analyte. In one embodiment, the kit comprises: (i) one or more reagents for transferring information from a first coding tag of a first binding agent to a first recording tag to generate a first extended recording tag, upon binding between the first binding agent and the analyte, (ii) one or more reagents for transferring information from a second coding tag of a second binding agent to a second recording tag to generate a second extended recording tag, upon binding between the second binding agent and the analyte, and / or (iii) one or more reagents for transferring information from a third (or higher order) coding tag of a third (or higher order) binding agent to a third (or higher order) recording tag to generate a third (or higher order) extended recording tag, upon binding between the third (or higher order) binding agent and the analyte, wherein the one or more reagents of (i), (ii), and / or (iii) can be the same or different.

[0016] In any of the preceding embodiments, the kit can further comprise (iii) one or more reagents for transferring information from a third (or higher order) coding tag of a third (or higher order) binding agent to a third (or higher order) recording tag to generate a third (or higher order) extended recording tag, upon binding between the third (or higher order) binding agent and the analyte.

[0017] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to associate directly or indirectly with the analyte.

[0018] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to be immobilized on a support.

[0019] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to co-localize with the analyte, for example, to allow transfer of information between the first, second, or third (or higher order) coding tag and the first, second, or third (or higher order) recording tag, respectively, upon binding between the first, second, or third (or higher order) binding agent and the analyte.

[0020] In any of the preceding embodiments, each of the first coding tag, the second coding tag, and / or the third (or higher order) coding tag can comprise a binding cycle specific barcode, such as a binding cycle specific spacer sequence C«, and / or a coding tag specific spacer sequence C«, wherein n is an integer and C« indicates binding between the rP1binding agent and the polypeptide. Alternatively, a binding cycle tag C« may be added exogenously, for example, the binding cycle tag C« may be exogenous to the coding tag(s).

[0021] In any of the preceding embodiments, the analyte can comprise a polypeptide. In one embodiment, the binding moiety of the kit is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the polypeptide, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent.

[0022] In any of the preceding embodiments, the kit can further comprise one or more of the functionalizing reagent.

[0023] In any of the preceding embodiments, the kit can further comprise an eliminating reagent for removing {e.g., by chemical cleavage or enzymatic cleavage) the one or more N-terminal, internal, or C-terminal amino acids of the polypeptide, or removing the functionalized N-terminal, internal, or C-terminal amino acid(s), optionally wherein the eliminating reagent comprises a carboxypeptidase or an aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; a mild Edman degradation reagent; an Edmanase enzyme; anhydrous TFA, a base; or any combination thereof.

[0024] In any of the preceding embodiments, the one or more N-terminal, internal, or C- terminal amino acids can comprise: (i) an N-terminal amino acid (NTAA); (ii) an N-terminal dipeptide sequence; (iii) an N-terminal tripeptide sequence; (iv) an internal amino acid; (v) an internal dipeptide sequence; (vi) an internal tripeptide sequence; (vii) a C-terminal amino acid (CTAA); (viii) a C-terminal dipeptide sequence; or (ix) a C-terminal tripeptide sequence, or any combination thereof, optionally wherein any one or more of the amino acid residues in (i)-(ix) are modified or functionalized.

[0025] In another aspect, disclosed herein is a kit, comprising: at least (a) a first binding agent comprising (i) a first binding moiety capable of binding to an N-terminal amino acid (NTAA) or a functionalized NTAA of a polypeptide to be analyzed, and (ii) a first coding tag comprising identifying information regarding the first binding moiety, optionally (b) a recording tag configured to associate directly or indirectly with the polypeptide, and further optionally (c) a functionalizing reagent capable of modifying a first NTAA of the polypeptide to generate a first functionalized NTAA, wherein the recording tag and the first binding agent are configured to allow transfer of information between the first coding tag and the recording tag, upon binding between the first binding agent and the polypeptide. In one embodiment, the kit further comprises one or more reagents for transferring information from the first coding tag to the recording tag, thereby generating a first order extended recording tag.

[0026] In any of the preceding embodiments, the functionalizing reagent can comprise a chemical agent, an enzyme, and / or a biological agent, such as an isothiocyanate derivative, 2,4- dinitrobenzenesulfonic (DNBS), 4-sulfonyl-2-nitrofluorobenzene (SNFB) l-fluoro-2,4- dinitrobenzene, dansyl chloride, 7-methoxycoumarin acetic acid, a thioacylation reagent, a thioacetylation reagent, or a thiobenzylation reagent.

[0027] In any of the preceding embodiments, the kit can further comprise an eliminating reagent for removing (e.g., by chemical cleavage or enzymatic cleavage) the first functionalized NTAA to expose the immediately adjacent amino acid residue, as a second NTAA. In one embodiment, the second NTAA is capable of being functionalized by the same or a different functionalizing reagent to generate a second functionalized NTAA, which may be the same as or different from the first functionalized NTAA. In another embodiment, the kit further comprises: (d) a second (or higherorder) binding agent comprising (i) a second (or higher order) binding moiety capable of binding to the second functionalized NTAA, and (ii) a second (or higher order) coding tag comprising identifying information regarding the second (or higher order) binding moiety, wherein the first coding tag and the second (or higher order) coding tag can be the same or different. In yet another embodiment, the first functionalized NTAA and the second functionalized NTAA are selected, independent from each other, from the group consisting of a functionalized N-terminal Alanine (A or Ala), Cysteine (C or Cys), Aspartic Acid (D or Asp), Glutamic Acid (E or Glu), Phenylalanine (F or Phe), Glycine (G or Gly), Histidine (H or His), Isoleucine (I or He), Lysine (K or Lys), Leucine (L or Leu), Methionine (M or Met), Asparagine (N or Asn), Proline (P or Pro), Glutamine (Q or Gin), Arginine (R or Arg), Serine (S or Ser), Threonine (T or Thr), Valine (V or Val), Tryptophan (W or Tip), and Tyrosine (Y or Tyr), in any combination thereof.

[0028] In any of the preceding embodiments, the kit can further comprise one or more reagents for transferring information from the second (or higher order) coding tag to the first order extended recording tag, thereby generating a second (or higher order) order extended recording tag.

[0029] In a further aspect, disclosed herein is a kit, comprising: at least (a) one or more binding agents each comprising (i) a binding moiety capable of binding to an N-terminal amino acid (NTAA) or a functionalized NTAA of a polypeptide to be analyzed, and (ii) a coding tag comprising identifying information regarding the binding moiety, and / or (b) one or more recording tags configured to associate directly or indirectly with the polypeptide, wherein the one or more recording tags and the one or more binding agents are configured to allow transfer of information between the coding tags and the recording tags, upon binding between each binding agent and the polypeptide, and optionally (c) a functionalizing reagent capable of modifying a first NTAA of the polypeptide to generate a first functionalized NTAA. In one embodiment, kit further comprises an eliminating reagent for removing (e.g., by chemical cleavage or enzymatic cleavage) the first functionalized NTAA to expose the immediately adjacent amino acid residue, as a second NTAA. In another embodiment, the second NTAA is capable of being functionalized by the same or a different functionalizing reagent to generate a second functionalized NTAA, which may be the same as or different from the first functionalized NTAA. In yet another embodiment, the first functionalized NTAA and the second functionalized NTAA are selected, independent from eachother, from the group consisting of a functionalized N-terminal Alanine (A or Ala), Cysteine (C or Cys), Aspartic Acid (D or Asp), Glutamic Acid (E or Glu), Phenylalanine (F or Phe), Glycine (G or Gly), Histidine (H or His), Isoleucine (I or He), Lysine (K or Lys), Leucine (L or Leu), Methionine (M or Met), Asparagine (N or Asn), Proline (P or Pro), Glutamine (Q or Gin), Arginine (R or Arg), Serine (S or Ser), Threonine (T or Thr), Valine (V or Val), Tryptophan (W or Trp), and Tyrosine (Y or Tyr), in any combination thereof.

[0030] In any of the preceding embodiments, the kit can comprise: (i) one or more reagents for transferring information from a first coding tag of a first binding agent to a first recording tag to generate a first extended recording tag, upon binding between the first binding agent and the polypeptide, and / or (ii) one or more reagents for transferring information from a second coding tag of a second binding agent to a second recording tag to generate a second extended recording tag, upon binding between the second binding agent and the polypeptide, wherein the one or more reagents of (i) and the one or more reagents of (ii) can be the same or different. In one aspect, the kit further comprises: (iii) one or more reagents for transferring information from a third (or higher order) coding tag of a third (or higher order) binding agent to a third (or higher order) recording tag to generate a third (or higher order) extended recording tag, upon binding between the third (or higher order) binding agent and the polypeptide.

[0031] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to associate directly or indirectly with the polypeptide.

[0032] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to be immobilized on a support.

[0033] In any of the preceding embodiments, the first recording tag, the second recording tag, and / or the third (or higher order) recording tag can be configured to co-localize with thepolypeptide, for example, to allow transfer of information between the first, second, or third (or higher order) coding tag and the first, second, or third (or higher order) recording tag, respectively, upon binding between the first, second, or third (or higher order) binding agent and the polypeptide.

[0034] In any of the preceding embodiments, the distance between or among the first recording tag, the second recording tag, and / or the third (or higher order) recording tag on the support can beequal to or greater than about 10 nm, equal to or greater than about 15 nm, equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, or equal to or greater than about 500 nm, while each recording tag and its corresponding analyte is configured to co-localize when both are immobilized to the support, or while the distance between each recording tag and its corresponding analyte is less than about 10"6nm, about 10"6nm, about 10"5nm, about 10"4nm, about 0.001 nm, about 0.01 nm, about 0.1 nm, about 0.5 nm, about 1 nm, about 2 nm, about 5 nm, or more than about 5 nm, or of any value in between the above ranges.

[0035] In any of the preceding embodiments, each of the first coding tag, the second coding tag, and / or the third (or higher order) coding tag can comprise a binding cycle specific barcode, such as a binding cycle specific spacer sequence C«, and / or a coding tag specific spacer sequence C«, wherein n is an integer and C« indicates binding between the rP1binding agent and the polypeptide. Alternatively, a binding cycle tag C« may be added exogenously, for example, the binding cycle tag C« may be exogenous to the coding tag(s).

[0036] In any of the preceding embodiments, the analyte or the polypeptide can comprise a protein or a polypeptide chain or a fragment thereof, a lipid, a carbohydrate, or a macrocycle, or a combination or complex thereof.

[0037] In any of the preceding embodiments, the analyte or the polypeptide can comprise a macromolecule or a complex thereof, such as a protein complex or subunit thereof.

[0038] In any of the preceding embodiments, the recording tag can comprise a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, a DNA or RNA with one more protected bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0039] In any of the preceding embodiments, the recording tag can comprise a universal priming site.

[0040] In any of the preceding embodiments, the recording tag can comprise a priming site for amplification, sequencing, or both, for example, the universal priming site comprises a priming site for amplification, sequencing, or both.

[0041] In any of the preceding embodiments, the recording tag and / or the coding tag can comprise a unique molecule identifier (UMI).

[0042] In any of the preceding embodiments, the recording tag and / or the coding tag can comprise a barcode and / or a nuclease site, such as a nicking endonuclease site (e.g., a dsDNA nicking endonuclease site).

[0043] In any of the preceding embodiments, the recording tag and / or the coding tag comprises a spacer at its 3 '-terminus and / or at its 5'-terminus, for example, the recording tag comprises a spacer at its 3 '-terminus.

[0044] In any of the preceding embodiments, the recording tag and / or the coding tag can comprise one or more nuclease sites, such as an endonuclease site, a homing endonuclease site, a restriction enzyme digestion site, a nicking endonuclease site, or a combination thereof. In some embodiments, a nuclease site can be provided in the coding tag, for example, within the spacer sequence or between the spacer sequence and the encoder sequence. In some embodiments, a nuclease site can be provided in the recording tag, for example, between the universal primer sequence and the support (e.g., for cleaving the recording tag off the support).

[0045] In any of the preceding embodiments, the kit can comprise a solid support, such as a rigid solid support, a flexible solid support, or a soft solid support, and including a porous support or a non-porous support.

[0046] In any of the preceding embodiments, the kit can comprise a support which comprises a bead, a porous bead, a porous matrix, an array, a surface, a glass surface, a silicon surface, a plastic surface, a slide, a filter, nylon, a chip, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a well, a microtitre well, a plate, an ELISA plate, a disc, a spinning interferometry disc, a membrane, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle (e.g., comprising a metal such as magnetic nanoparticles (Fe304), gold nanoparticles, and / or silver nanoparticles), quantum dots, a nanoshell, a nanocage, a microsphere, or any combination thereof. In one embodiment, the support comprises a polystyrene bead, a polymerbead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead, or any combination thereof.

[0047] In any of the preceding embodiments, the kit can comprise a support and / or can be for analyzing a plurality of the analytes (such as polypeptides), in sequential reactions, in parallel reactions, or in a combination of sequential and parallel reactions. In one embodiment, the analytes are spaced apart on the support at an average distance equal to or greater than about 10 nm, equal to or greater than about 15 nm, equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, or equal to or greater than about 500 nm.

[0048] In any of the preceding embodiments, the binding moiety can comprise a polypeptide or fragment thereof, a protein or polypeptide chain or fragment thereof, or a protein complex or subunit thereof, such as an antibody or antigen binding fragment thereof.

[0049] In any of the preceding embodiments, the binding moiety can comprise acarboxypeptidase or an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS or variant, mutant, or modified protein thereof; a UBR box protein or variant, mutant, or modified protein thereof; a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or any combination thereof, or wherein in each binding agent, the binding moiety comprises a small molecule, the coding tag comprises a polynucleotide that identifies the small molecule, whereby a plurality of the binding agents form an encoded small molecule library, such as a DNA-encoded small molecule library.

[0050] In any of the preceding embodiments, the binding moiety can selectively and / or specifically bind to the analyte or the polypeptide.

[0051] In any of the preceding embodiments, the coding tag can comprise a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, a DNA or RNA with one or more protected bases, an RNA molecule, a BNA molecule, anXNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0052] In any of the preceding embodiments, the coding tag can comprise a barcode sequence, such as an encoder sequence, e.g., one that identifies the binding moiety.

[0053] In any of the preceding embodiments, the coding tag can comprise a spacer, a binding cycle specific sequence, a unique molecular identifier (UMI), a universal priming site, or any combination thereof. In one embodiment, a binding cycle specific sequence is added to the recording tag after each binding cycle.

[0054] In any of the preceding embodiments, the binding moiety and the coding tag can be joined by a linker or a binding pair.

[0055] In any of the preceding embodiments, the binding moiety and the coding tag can be joined by a Spy Tag / Spy Catcher, a Spy Tag-KTag / Spy Ligase (where two moieties to be joined have the SpyTag / KTag pair, and the SpyLigase joins SpyTag to KTag, thus joining the two moieties), a SnoopTag / SnoopCatcher peptide-protein pair, a HaloTag / HaloTag ligand pair, or a sortase, such as a LPXTG Tag / Sortase (e.g., Sortase A5, ActiveMotif, San Diego, or as disclosed in US 9,267, 127 B2 which is incorporated herein by reference), or any combination thereof.

[0056] In any of the preceding embodiments, the kit can further comprise a reagent for transferring information between the coding tag and the recording tag in a templated or non- templated reaction, optionally wherein the reagent is (i) a chemical ligation reagent or a biological ligation reagent, for example, a ligase, such as a DNA ligase or RNA ligase for ligating single- stranded nucleic acid or double-stranded nucleic acid, or (ii) a reagent for primer extension of single-stranded nucleic acid or double-stranded nucleic acid, optionally wherein the kit further comprises a ligation reagent comprising at least two ligases or variants thereof (e.g., at least two DNA ligases, or at least two RNA ligases, or at least one DNA ligase and at least one RNA ligase), wherein the at least two ligases or variants thereof comprises an adenylated ligase and a constitutively non-adenylated ligase, or optionally wherein the kit further comprises a ligation reagent comprising a DNA or RNA ligase and a DNA / RNA deadenylase.

[0057] In any of the preceding embodiments, the kit can further comprise a polymerase, such as a DNA polymerase or RNA polymerase or a reverse transcriptase, for transferring information between the coding tag and the recording tag.

[0058] In any of the preceding embodiments, the kit can further comprise one or more reagents for nucleic acid sequence analysis. In one embodiment, the nucleic acid sequence analysis comprises sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, pyrosequencing, single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy, or any combination thereof.

[0059] In any of the preceding embodiments, the kit can further comprise one or more reagents for nucleic acid amplification, for example, for amplifying one or more extended recording tags, optionally wherein the nucleic acid amplification comprises an exponential amplification reaction (e.g., polymerase chain reaction (PCR), such as an emulsion PCR to reduce or eliminate template switching) and / or a linear amplification reaction (e.g., isothermal amplification by in vitro transcription, or Isothermal Chimeric primer-initiated Amplification of Nucleic acids (ICAN)). See e.g., Uemori et al., (2007), "Investigation of the molecular mechanism of ICAN, a novel gene amplification method," J Biochem 142(2): 283-292; Mukai et al., (2007), "Highly efficient isothermal DNA amplification system using three elements of 5'-DNA-RNA-3' chimeric primers, RNaseH and strand-displacing DNA polymerase," J Biochem 142(2): 273-281; Ma et al., (2013), "Isothermal amplification method for next-generation sequencing," Proc Natl Acad Sci USA. 110(35): 14320-14323, all of which are incorporated herein by reference for all purposes.

[0060] In any of the preceding embodiments, the kit can comprise one or more reagents for transferring coding tag information to the recording tag to form an extended recording tag, wherein the order and / or frequency of coding tag information on the extended recording tag indicates the order and / or frequency in which the binding agent binds to the analyte or the polypeptide.

[0061] In any of the preceding embodiments, the kit can further comprise one or more reagents for target enrichment, for example, enrichment of one or more extended recording tags.

[0062] In any of the preceding embodiments, the kit can further comprise one or more reagents for subtraction, for example, subtraction of one or more extended recording tags.

[0063] In any of the preceding embodiments, the kit can further comprise one or more reagents for normalization, for example, to reduce highly abundant species such as one or more analytes or polypeptides.

[0064] In any of the preceding embodiments, at least one binding agent of the kit can bind to a terminal amino acid residue, terminal di-amino-acid residues, or terminal triple-amino-acid residues.

[0065] In any of the preceding embodiments, at least one binding agent of the kit can bind to a post-translationally modified amino acid.

[0066] In any of the preceding embodiments, the kit can further comprise one or more reagents or means for partitioning a plurality of the analytes or polypeptides in a sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags optionally joined to a support (e.g., a solid support), wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of othercompartments. In one embodiment, the kit further comprises one or more reagents or means for fragmenting the plurality of the analytes or polypeptides (such as a plurality of protein complexes, proteins, and / or polypeptides) into a plurality of polypeptide fragments.

[0067] In any of the preceding embodiments, the kit can further comprise one or more reagents or means for annealing or joining of the plurality of polypeptide fragments with the compartment tag within each of the plurality of compartments, thereby generating a plurality of compartment tagged polypeptide fragments.

[0068] In any of the preceding embodiments, the plurality of compartments can comprise a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof.

[0069] In any of the preceding embodiments, each of the plurality of compartments can comprise on average a single cell.

[0070] In any of the preceding embodiments, the kit can further comprise one or more universal DNA tags for labeling the plurality of the analytes or polypeptides in the sample.

[0071] In any of the preceding embodiments, the kit can further comprise one or more reagents for labeling the plurality of the analytes or polypeptides in the sample with one or more universal DNA tags.

[0072] In any of the preceding embodiments, the kit can further comprise one or more reagents for primer extension or ligation.

[0073] In any of the preceding embodiments, the support can comprise a bead, such as a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead, or any combination thereof.

[0074] In any of the preceding embodiments, the compartment tag can comprise a single stranded or double stranded nucleic acid molecule.

[0075] In any of the preceding embodiments, the compartment tag can comprise a barcode and optionally a UMI. In any of the preceding embodiments, the support can be a bead and the compartment tag can comprise a barcode.

[0076] In any of the preceding embodiments, the support can comprise a bead, and beads comprising the plurality of compartment tags joined thereto can be formed by split-and-pool synthesis, individual synthesis, or immobilization, or any combination thereof.

[0077] In any of the preceding embodiments, the kit can further comprise one or more reagents for split-and-pool synthesis, individual synthesis, or immobilization, or any combination thereof.

[0078] In any of the preceding embodiments, the compartment tag can be a component within a recording tag, wherein the recording tag optionally can further comprise a spacer, a barcode sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0079] In any of the preceding embodiments, the compartment tags can further comprise a functional moiety capable of reacting with an internal amino acid, the peptide backbone, or N- terminal amino acid on the plurality of analytes or polypeptides (such as protein complexes, proteins, or polypeptides). In one embodiment, the functional moiety can comprise an aldehyde, an azide / alkyne, a malemide / thiol, an epoxy / nucleophile, an inverse Electron Demand Diels-Alder (iEDDA) group, a click reagent, or any combination thereof.

[0080] In any of the preceding embodiments, the compartment tag can further comprise a peptide, such as a protein ligase recognition sequence, and optionally the protein ligase can be butelase I or a homolog thereof.

[0081] In any of the preceding embodiments, the kit can further comprise a chemical or biological reagent, such as an enzyme, for example, a protease (e.g., a metalloprotease), for fragmenting the plurality of analytes or polypeptides.

[0082] In any of the preceding embodiments, the kit can further comprise one or more reagents for releasing the compartment tags from the support.

[0083] In any of the preceding embodiments, the kit can further comprise one or more reagents for forming an extended coding tag or a di-tag construct. In one embodiment, the 3 '-terminus of the recording tag is blocked to prevent extension of the recording tag by a polymerase. In any of the preceding embodiments, the coding tag can comprise an encoder sequence, a UMI, a universal priming site, a spacer at its 3 '-terminus, a binding cycle specific sequence, or any combination thereof.

[0084] In any of the preceding embodiments, the di-tag construct can be generated by gap fill, primer extension, or a combination thereof.

[0085] In any of the preceding embodiments, the di-tag molecule can comprise a universal priming site derived from the recording tag, a compartment tag derived from the recording tag, a unique molecular identifier derived from the recording tag, an optional spacer derived from the recording tag, an encoder sequence derived from the coding tag, a unique molecular identifier derived from the coding tag, an optional spacer derived from the coding tag, and a universal priming site derived from the coding tag.

[0086] In any of the preceding embodiments, the binding agent can be a polypeptide or protein.

[0087] In any of the preceding embodiments, the binding agent can comprise an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof (such as a vancomycin that binds to D-alanyl-D-alanine); or an antibody or binding fragment thereof; or any combination thereof.

[0088] In any of the preceding embodiments, the binding agent can bind to a single amino acid residue (e.g., an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue), a dipeptide (e.g., an N-terminal dipeptide, a C-terminal dipeptide, or aninternal dipeptide), a tripeptide (e.g., an N-terminal tripeptide, a C-terminal tripeptide, or an internal tripeptide), or a post-translational modification of the analyte or polypeptide.

[0089] In any of the preceding embodiments, the binding agent can bind to an N-terminal polypeptide, a C-terminal polypeptide, or an internal polypeptide.

[0090] In any of the preceding embodiments, the coding tag and / or the recording tag can comprise one or more error correcting codes, one or more encoder sequences, one or more barcodes, one or more UMIs, one or more compartment tags, one or more cycle specific sequences, or any combination thereof. In some embodiments, the error correcting code is selected from Hamming code, Lee distance code, asymmetric Lee distance code, Reed-Solomon code, and Levenshtein-Tenengolts code.

[0091] In any of the preceding embodiments, the coding tag and / or the recording tag can comprise a cycle label.

[0092] In any of the preceding embodiments, the kit can further comprise a cycle label independent of the coding tag and / or the recording tag.

[0093] In any of the preceding embodiments, the kit can further comprise: (a) a reagent for generating a cell lysate or a protein sample; (b) a reagent for blocking an amino acid side chain, such as via alkylation of cysteine or blocking lysine; (c) a protease, such as trypsin, LysN, or LysC; (d) a reagent for immobilizing a nucleic acid-labeled polypeptide (such as a DNA-labeled protein) to a support; (e) a reagent for degradation-based polypeptide sequencing; and / or (f) a reagent for nucleic acid sequencing.

[0094] In any of the preceding embodiments, the kit can comprise: (a) a reagent for generating a cell lysate or a protein sample; (b) a reagent for blocking an amino acid side chain, such as via alkylation of cysteine or blocking lysine; (c) a protease, such as trypsin, LysN, or LysC; (d) a reagent for immobilizing a polypeptide (such as a protein) to a support comprising immobilized recording tags; (e) a reagent for degradation-based polypeptide sequencing; and / or (f) a reagent for nucleic acid sequencing.

[0095] In any of the preceding embodiments, the kit can comprise: (a) a reagent for generating a cell lysate or a protein sample; (b) a denaturing reagent; (c) a reagent for blocking an amino acid side chain, such as via alkylation of cysteine or blocking lysine; (d) a universal DNA primersequence; (e) a reagent for labeling a polypeptide with a universal DNA primer sequence; (f) a barcoded bead for annealing the labeled polypeptide via a primer; (g) a reagent for polymerase extension for writing the barcode from the bead to the labeled polypeptide; (h) a protease, such as trypsin, LysN, or LysC; (i) a reagent for immobilizing a nucleic acid-labeled polypeptide (such as a DNA-labeled protein) to a support; (j) a reagent for degradation-based polypeptide sequencing; and / or (k) a reagent for nucleic acid sequencing.

[0096] In any of the preceding embodiments, the kit can comprise:(a) a cross-linking reagent; (b) a reagent for generating a cell lysate or a protein sample; (c) a reagent for blocking an amino acid side chain, such as via alkylation of cysteine or blocking lysine; (d) a universal DNA primer sequence; (e) a reagent for labeling a polypeptide with a universal DNA primer sequence; (f) a barcoded bead for annealing the labeled polypeptide via a primer; (g) a reagent for polymerase extension for writing the barcode from the bead to the labeled polypeptide; (h) a protease, such as trypsin, LysN, or LysC; (i) a reagent for immobilizing a nucleic acid-labeled polypeptide (such as a DNA-labeled protein) to a support; (j) a reagent for degradation-based polypeptide sequencing; and / or (k) a reagent for nucleic acid sequencing.

[0097] In any of the preceding embodiments of the kit, one or more components can be provided in a solution or on a support, for example, a solid support.

[0098] Kit components may also include any molecule, molecular complex or conjugate, reagent (e.g., chemical or biological), agent, structure (e.g., support, surface, particle, or bead), reaction intermediate, reaction product, binding complex, or any other article of manufacture disclosed and / or used in the following exemplary methods and / or aspects. The present kits can be used for analyzing any suitable analyte, e.g., a macromolecule or a polypeptide. In some embodiments, the present kits can be used for highly-parallel, high throughput digital analysis (e.g., a macromolecule analysis), particularly polypeptide analysis. In some embodiments, the present kits can be used in the following exemplary methods for analyzing an analyte, e.g., amacromolecule or a polypeptide.

[0099] In a first Example is a method for analyzing an analyte, e.g., a macromolecule or a polypeptide, comprising the steps of: (a) providing an analyte and an associated recording tag joined to a solid support; (b) contacting the an analyte with a first binding agent capable of binding to theanalyte, wherein the first binding agent comprises a first coding tag with identifying information regarding the first binding agent; (c) transferring the information of the first coding tag to the recording tag to generate a first order extended recording tag; (d) contacting the analyte with a second binding agent capable of binding to the analyte, wherein the second binding agent comprises a second coding tag with identifying information regarding the second binding agent; (e) transferring the information of the second coding tag to the first order extended recording tag to generate a second order extended recording tag; and (f) analyzing the second order extended recording tag.

[0100] In a second Example is the method of the first Example, wherein contacting steps (b) and (d) are performed in sequential order.

[0101] In a third Example is the method of the first Example, where wherein contacting steps (b) and (d) are performed at the same time.

[0102] In a fourth Example is the method of the first Example, further comprising, between steps (e) and (f), the following steps: (x) repeating steps (d) and (e) one or more times by replacing the second binding agent with a third (or higher order) binding agent capable of binding to the analyte, wherein the third (or higher order) binding agent comprises a third (or higher order) coding tag with identifying information regarding the third (or higher order) bind agent; and (y) transferring the information of the third (or higher order) coding tag to the second (or higher order) extended recording tag to generate a third (or higher order) extended recording tag; and wherein the third (or higher order) extended recording tag is analyzed in step (f).

[0103] In a fifth Example is a method for analyzing an analyte, e.g., a macromolecule or a polypeptide, comprising the steps of: (a) providing an analyte, an associated first recording tag and an associated second recording tag joined to a solid support; (b) contacting the analyte with a first binding agent capable of binding to the analyte, wherein the first binding agent comprises a first coding tag with identifying information regarding the first binding agent; (c) transferring the information of the first coding tag to the first recording tag to generate a first extended recording tag; (d) contacting the analyte with a second binding agent capable of binding to the analyte, wherein the second binding agent comprises a second coding tag with identifying information regarding the second binding agent; (e) transferring the information of the second coding tag to thesecond recording tag to generate a second extended recording tag; and (f) analyzing the first and second extended recording tags.

[0104] In a sixth Example is the method of fifth Example, wherein contacting steps (b) and (d) are performed in sequential order.

[0105] In a seventh Example is the method of the fifth Example, wherein contacting steps (b) and (d) are performed at the same time.

[0106] In an eight Example is the method of fifth Example, wherein step (a) further comprises providing an associated third (or higher odder) recording tag joined to the solid support.

[0107] In a ninth Example is the method of the eighth Example, further comprising, between steps (e) and (f), the following steps: (x) repeating steps (d) and (e) one or more times by replacing the second binding agent with a third (or higher order) binding agent capable of binding to the analyte, wherein the third (or higher order) binding agent comprises a third (or higher order) coding tag with identifying information regarding the third (or higher order) bind agent; and (y)transferring the information of the third (or higher order) coding tag to the third (or higher order) recording tag to generate a third (or higher order) extended recording tag; and wherein the first, second and third (or higher order) extended recording tags are analyzed in step (f).

[0108] In a 10thExample is the method of any one of the fifth to ninth Examples, wherein the first coding tag, second coding tag, and any higher order coding tags comprise a binding cycle specific spacer sequence.

[0109] In an 11thExample is a method for analyzing a peptide, comprising the steps of: (a) providing a peptide and an associated recording tag joined to a solid support; (b) modifying the N- terminal amino acid (NTAA) of the peptide with a chemical agent; (c) contacting the peptide with a first binding agent capable of binding to the modified NTAA, wherein the first binding agent comprises a first coding tag with identifying information regarding the first binding agent; (d) transferring the information of the first coding tag to the recording tag to generate an extended recording tag; and (e) analyzing the extended recording tag.

[0110] In a 12thExample is the method of 11thExample, wherein step (c) further comprises contacting the peptide with a second (or higher order) binding agent comprising a second (or higher order) coding tag with identifying information regarding the second (or higher order) binding agent,wherein the second (or higher order) binding agent is capable of binding to a modified NTAA other than the modified NTAA of step (b).

[0111] In a 13thExample is the method of the 12thExample, wherein contacting the peptide with the second (or higher order) binding agent occurs in sequential order following the peptide being contacted with the first binding agent.

[0112] In a 14thExample is the method of 12thExample, wherein contacting the peptide with the second (or higher order) binding agent occurs simultaneously with the peptide being contacted with the first binding agent.

[0113] In a 15thExample is the method of any one the 11th- 14thExamples, wherein the chemical agent is an isothiocyanate derivative, 2,4-dinitrobenzenesulfonic (DNBS), 4-sulfonyl-2- nitrofluorobenzene (SNFB) l-fluoro-2,4-dinitrobenzene, dansyl chloride, 7-methoxycoumarin acetic acid, a thioacylation reagent, a thioacetylation reagent, or a thiobenzylation reagent.

[0114] In a 16thExample is a method for analyzing a peptide, comprising the steps of: (a) providing a peptide and an associated recording tag joined to a solid support; (b) modifying the N- terminal amino acid (NTAA) of the peptide with a chemical agent to yield a modified NTAA; (c) contacting the peptide with a first binding agent capable of binding to the modified NTAA, wherein the first binding agent comprises a first coding tag with identifying information regarding the first binding agent; (d) transferring the information of the first coding tag to the recording tag to generate a first extended recording tag; (e) removing the modified NTAA to expose a new NTAA; (f) modifying the new NTAA of the peptide with a chemical agent to yield a newly modified NTAA; (g) contacting the peptide with a second binding agent capable of binding to the newly modified NTAA, wherein the second binding agent comprises a second coding tag with identifying information regarding the second binding agent; (h) transferring the information of the second coding tag to the first extended recording tag to generate a second extended recording tag; and (i) analyzing the second extended recording tag.

[0115] In a 17thExample is a method for analyzing a peptide, comprising the steps of: (a) providing a peptide and an associated recording tag joined to a solid support; (b) contacting the peptide with a first binding agent capable of binding to the N-terminal amino acid (NTAA) of the peptide, wherein the first binding agent comprises a first coding tag with identifying informationregarding the first binding agent; (c) transferring the information of the first coding tag to the recording tag to generate an extended recording tag; and (d) analyzing the extended recording tag.

[0116] In an 18thExample is the method of the 17thExample, wherein step (b) further comprises contacting the peptide with a second (or higher order) binding agent comprising a second (or higher order) coding tag with identifying information regarding the second (or higher order) binding agent, wherein the second (or higher order) binding agent is capable of binding to a NTAA other than the NTAA of the peptide.

[0117] In a 19thExample is the method of the 18thExample, wherein contacting the peptide with the second (or higher order) binding agent occurs in sequential order following the peptide being contacted with the first binding agent.

[0118] In a 20thExample is the method of the 18thExample, wherein contacting the peptide with the second (or higher order) binding agent occurs simultaneously with the peptide being contacted with the first binding agent.

[0119] In a 21stExample is a method for analyzing a peptide, comprising the steps of: (a) providing a peptide and an associated recording tag joined to a solid support; (b) contacting the peptide with a first binding agent capable of binding to the N-terminal amino acid (NTAA) of the peptide, wherein the first binding agent comprises a first coding tag with identifying information regarding the first binding agent; (c) transferring the information of the first coding tag to the recording tag to generate a first extended recording tag; (d) removing the NTAA to expose a new NTAA of the peptide; (e) contacting the peptide with a second binding agent capable of binding to the new NTAA, wherein the second binding agent comprises a second coding tag with identifying information regarding the second binding agent; (f) transferring the information of the second coding tag to the first extended recording tag to generate a second extended recording tag; and (g) analyzing the second extended recording tag.

[0120] In a 22ndExample is the method of any one of the first- 10thExamples, wherein the analyte is a protein, polypeptide or peptide.

[0121] In a 23rdExample is the method of any one of the first- 10thExamples, wherein the analyte is a peptide.

[0122] In a 24 Example is the method of any one of the 11 -23 Examples, wherein the peptide is obtained by fragmenting a protein from a biological sample.

[0123] In a 25thExample is the method of any one of the first-lO111Examples, wherein the analyte is a lipid, a carbohydrate, or a macrocycle.

[0124] In a 26thExample is the method of any one of the first^S111Examples, wherein the recording tag is a DNA molecule, DNA with pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0125] In a 27thExample is the method of any one of the firsts111Examples, wherein the recording tag comprises a universal priming site.

[0126] In a 28thExample is the method of the 27thExample, wherein the universal priming site comprises a priming site for amplification, sequencing, or both.

[0127] In a 29thExample is the method of the first-28thExamples, where the recording tag comprises a unique molecule identifier (UMI).

[0128] In a 30thExample is the method of any one of the firsts"1Examples, wherein the recording tag comprises a barcode.

[0129] In a 31stExample is the method of any one of the first-SO111Examples, wherein the recording tag comprises a spacer at its 3 '-terminus.

[0130] In a 32ndExample is the method of any one of the first-31stExamples, wherein the analyte and the associated recording tag are covalently joined to the solid support.

[0131] In a 33rdExample is the method of any one of the first-32ndExamples, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinninginterferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0132] In a 34thExample is the method of the 33rdExample, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0133] In a 35 Example is the method of any one of the first-34 Examples, wherein a plurality of analytes (e.g., molecules of the same analyte or of different analytes) and associated recording tags are joined to a solid support.

[0134] In a 36thExample is the method of the 35thExample, wherein the plurality of analytes (e.g., molecules of the same analyte or of different analytes) are spaced apart on the solid support at an average distance > 50 nm.

[0135] In a 37thExample is the method of any one of first-Se"1Examples, wherein the binding agent is a polypeptide or protein.

[0136] In a 38thExample is the method of the 37thExample, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or a modified ClpS.

[0137] In a 39thExample is the method of any one of the first-SS111Examples, wherein the binding agent is capable of selectively binding to the analyte.

[0138] In a 40thExample is the method of any one of the firsts"1Examples, wherein the coding tag is DNA molecule, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0139] In a 41stExample is the method of any one of the first-40thExamples, wherein the coding tag comprises an encoder sequence.

[0140] In a 42ndExample is the method of any one of the first-41stExamples, wherein the coding tag further comprises a spacer, a binding cycle specific sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0141] In a 43rdExample is the method of any one of the first-42ndExamples, wherein the binding agent and the coding tag are joined by a linker.

[0142] In a 44thExample is the method of any one of the first-42ndExamples, wherein the binding agent and the coding tag are joined by a Spy Tag / Spy Catcher, a SpyTag-KTag / SpyLigase (where two moieties to be joined have the SpyTag / KTag pair, and the SpyLigase joins SpyTag to KTag, thus joining the two moieties), a sortase, or SnoopTag / SnoopCatcher peptide-protein pair.

[0143] In a 45thExample is the method of any one of the first-44thExamples, wherein transferring the information of the coding tag to the recording tag is mediated by a DNA ligase.

[0144] In a 46 Example is the method of any one of the first-44 Examples, wherein transferring the information of the coding tag to the recording tag is mediated by a DNApolymerase.

[0145] In a 47thExample is the method of any one of the first-44thExamples, wherein transferring the information of the coding tag to the recording tag is mediated by chemical ligation.

[0146] In a 48thExample is the method of any one of the firsts?"1Examples, wherein analyzing the extended recording tag comprises a nucleic acid sequencing method.

[0147] In a 49thExample is the method of the 48th Example, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing byhybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

[0148] In a 50thExample is the method of the 48thExample, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0149] In a 51stExample is the method of any one of the first-SO111Examples, wherein the extended recording tag is amplified prior to analysis.

[0150] In a 52ndExample is the method of any one of the first -51stExamples, wherein the order of coding tag information contained on the extended recording tag provides information regarding the order of binding by the binding agents to the analyte.

[0151] In a 53rdExample is the method of any one of the first-52ndExamples, wherein frequency of the coding tag information contained on the extended recording tag provides information regarding the frequency of binding by the binding agents to the analyte.

[0152] In a 54thExample is the method of any one of the first-53rdExamples, wherein a plurality of extended recording tags representing a plurality of analytes (e.g., molecules of the same analyte or of different analytes) are analyzed in parallel.

[0153] In a 55thExample is the method of the 54thExample, wherein the plurality of extended recording tags representing a plurality of analytes (e.g., molecules of the same analyte or of different analytes) are analyzed in a multiplexed assay.

[0154] In a 56thExample is the method of any one of the first-SS"1Examples, wherein the plurality of extended recording tags undergoes a target enrichment assay prior to analysis.

[0155] In a 57 Example is the method of any one of the first-56 Examples, wherein the plurality of extended recording tags undergoes a subtraction assay prior to analysis.

[0156] In a 58thExample is the method of any one of the first-57thExamples, wherein the plurality of extended recording tags undergoes a normalization assay to reduce highly abundant species prior to analysis.

[0157] In a 59thExample is the method of any one of the first-SS111Examples, wherein the NTAA is removed by a modified aminopeptidase, a modified amino acid tRNA synthetase, mild Edman degradation, Edmanase enzyme, or anhydrous TFA.

[0158] In a 60thExample is the method of any one of the firsts"1Examples, wherein at least one binding agent binds to a terminal amino acid residue.

[0159] In a 61stExample is the method of any one of the first-eo"1Examples, wherein at least one binding agent binds to a post-translationally modified amino acid.

[0160] In a 62ndExample is a method for analyzing one or more peptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising: (a) partitioning the plurality of protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags optionally joined to a solid support, wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments; (b) fragmenting the plurality of protein complexes, proteins, and / or polypeptides into a plurality of peptides; (c) contacting the plurality of peptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of peptides with the plurality of compartment tags within the plurality of compartments, thereby generating a plurality of compartment tagged peptides; (d) collecting the compartment tagged peptides from the plurality of compartments; and (e) analyzing one or more compartment tagged peptide according to a method of any one of the first-21stExamples and 26th-61stExamples.

[0161] In a 63rdExample is the method of the 62ndExample, wherein the compartment is a microfluidic droplet.

[0162] In a 64thExample is the method of the 62ndExample, wherein the compartment is a microwell.

[0163] In a 65 Example is the method of the 62 Example, wherein the compartment is a separated region on a surface.

[0164] In a 66thExample is the method of any one of the 62nd-65thExamples, wherein each compartment comprises on average a single cell.

[0165] In a 67thExample is a method for analyzing one or more peptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising: (a) labeling of the plurality of protein complexes, proteins, or polypeptides with a plurality of universal DNA tags; (b) partitioning the plurality of labeled protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags, wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments; (c) contacting the plurality of protein complexes, proteins, or polypeptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of protein complexes, proteins, or polypeptides with the plurality of compartment tags within the plurality of compartments, thereby generating a plurality of compartment tagged protein complexes, proteins or polypeptides; (d) collecting the compartment tagged protein complexes, proteins, or polypeptides from the plurality of compartments; (e) optionally fragmenting the compartment tagged protein complexes, proteins, or polypeptides into a compartment tagged peptides; and (f) analyzing one or more compartment tagged peptide according to a method of any one of the first- 21stExamples and 26th-61stExamples.

[0166] In a 68thExample is the method of any one of the 62nd-67thExamples, wherein compartment tag information is transferred to a recording tag associated with a peptide via primer extension or ligation.

[0167] In a 69thExample is the method of any one of the 62nd-68thExamples, wherein the solid support comprises a bead.

[0168] In a 70thExample is the method of the 69thExample, wherein the bead is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0169] In a 71stExample is the method of any one of the 62nd-70 Examples, wherein the compartment tag comprises a single stranded or double stranded nucleic acid molecule.

[0170] In a 72ndExample is the method of any one of the 62nd-71stExamples, wherein the compartment tag comprises a barcode and optionally a UMI.

[0171] In a 73rdExample is the method of the 72ndExample, wherein the solid support is a bead and the compartment tag comprises a barcode, further wherein beads comprising the plurality of compartment tags joined thereto are formed by split-and-pool synthesis.

[0172] In a 74thExample is the method of the 72ndExample, wherein the solid support is a bead and the compartment tag comprises a barcode, further wherein beads comprising a plurality of compartment tags joined thereto are formed by individual synthesis or immobilization.

[0173] In a 75thExample is the method of any one of the 62nd-74thExamples, wherein the compartment tag is a component within a recording tag, wherein the recording tag optionally further comprises a spacer, a unique molecular identifier, a universal priming site, or any combination thereof.

[0174] In a 76thExample is the method of any one of the 62nd-75thExamples, wherein the compartment tags further comprise a functional moiety capable of reacting with an internal amino acid or N-terminal amino acid on the plurality of protein complexes, proteins, or polypeptides.

[0175] In a 77thExample is the method of the 76thExample, wherein the functional moiety is an NHS group.

[0176] In a 78thExample is the method of the 76thExample, wherein the functional moiety is an aldehyde group.

[0177] In a 79thExample is the method of any one of the 62nd-78thExamples, wherein the plurality of compartment tags is formed by: printing, spotting, ink-jetting the compartment tags into the compartment, or a combination thereof.

[0178] In an 80thExample is the method of any one of the 62nd-79thExamples, wherein the compartment tag further comprises a peptide.

[0179] In an 81stExample is the method of the 80thExample, wherein the compartment tag peptide comprises a protein ligase recognition sequence.

[0180] In an 82 Example is the method of the 81stExample, wherein the protein ligase is butelase I or a homolog thereof.

[0181] In an 83rd. Example is the method of any one of the 62nd-82ndExamples, wherein the plurality of polypeptides is fragmented with a protease.

[0182] In an 84thExample is the method of the 83rdExample, wherein the protease is a metalloprotease.

[0183] In an 85thExample is the method of the 84thExample, wherein the activity of the metalloprotease is modulated by photo-activated release of metallic cations.

[0184] In an 86thExample is the method of any one of the 62nd-85thExamples, further comprising subtraction of one or more abundant proteins from the sample prior to partitioning the plurality of polypeptides into the plurality of compartments.

[0185] In an 87thExample is the method of any one of the 62nd-86thExamples, further comprising releasing the compartment tags from the solid support prior to joining of the plurality of peptides with the compartment tags.

[0186] In an 88thExample is the method of the 62ndExample, further comprising following step (d), joining the compartment tagged peptides to a solid support in association with recording tags.

[0187] In an 89thExample is the method of the 88thExample, further comprising transferring information of the compartment tag on the compartment tagged peptide to the associated recording tag.

[0188] In a 90thExample is the method of the 89thExample, further comprising removing the compartment tags from the compartment tagged peptides prior to step (e).

[0189] In a 91stExample is the method of any one of the 62nd-90thExamples, further comprising determining the identity of the single cell from which the analyzed peptide derived based on the analyzed peptide's compartment tag sequence.

[0190] In a 92ndExample is the method of any one of the 62nd-90thExamples, further comprising determining the identity of the protein or protein complex from which the analyzed peptide derived based on the analyzed peptide' s compartment tag sequence.

[0191] In a 93rdExample is a method for analyzing a plurality of analytes (e.g., molecules of the same analyte or of different analytes), comprising the steps of: (a) providing a plurality of analytesand associated recording tags joined to a solid support; (b) contacting the plurality of analytes with a plurality of binding agents capable of binding to the plurality of analytes, wherein each binding agent comprises a coding tag with identifying information regarding the binding agent; (c) (i) transferring the information of the analyte associated recording tags to the coding tags of the binding agents that are bound to the analytes to generate extended coding tags; or (ii) transferring the information of analyte associated recording tags and coding tags of the binding agents that are bound to the analytes to a di-tag construct; (d) collecting the extended coding tags or di-tag constructs; (e) optionally repeating steps (b) - (d) for one or more binding cycles; (f) analyzing the collection of extended coding tags or di-tag constructs.

[0192] In a 94thExample is the method of the 93rdExample, wherein the analyte is a protein.

[0193] In a 95thExample is the method of the 93rdExample, wherein the analyte is a peptide.

[0194] In a 96thExample is the method of the 95thExample, wherein the peptide is obtained by fragmenting a protein from a biological sample.

[0195] In a 97thExample is the method of any one of the 93rd-96thExamples, wherein the recording tag is a DNA molecule, an RNA molecule, a PNA molecule, a BNA molecule, an XNA, molecule, an LNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0196] In a 98thExample is the method of any one of the 93rd-97thExamples, wherein the recording tag comprises a unique molecular identifier (UMI).

[0197] In a 99thExample is the method of Examples 93-98, wherein the recording tag comprises a compartment tag.

[0198] In a 100thExample is the method of any one of Examples 93-99, wherein the recording tag comprises a universal priming site.

[0199] In a 101stExample is the method of any one of Examples 93-100, wherein the recording tag comprises a spacer at its 3 '-terminus.

[0200] In a 102ndExample is the method of any one of Examples 93-101, wherein the 3'- terminus of the recording tag is blocked to prevent extension of the recording tag by a polymerase and the information of analyte associated recording tag and coding tag of the binding agent that is bound to the analyte is transferred to a di-tag construct.

[0201] In a 103 Example is the method of any one of Examples 93-102, wherein the coding tag comprises an encoder sequence.

[0202] In a 104thExample is the method of any one of Examples 93-103, wherein the coding tag comprises a UMI.

[0203] In a 105thExample is the method of any one of Examples 93-104, wherein the coding tag comprises a universal priming site.

[0204] In a 106thExample is the method of any one of Examples 93-105, wherein the coding tag comprises a spacer at its 3 '-terminus.

[0205] In a 107thExample is the method of any one of Examples 93-106, wherein the coding tag comprises a binding cycle specific sequence.

[0206] In a 108thExample is the method of any one of Examples 93-107, wherein the binding agent and the coding tag are joined by a linker.

[0207] In a 109thExample is the method of any one of Examples 93-108, wherein transferring information of the recording tag to the coding tag is effected by primer extension.

[0208] In a 110thExample is the method of any one of Examples 93-108, wherein transferring information of the recording tag to the coding tag is effected by ligation.

[0209] In an 111thExample is the method of any one of Examples 93-108, wherein the di-tag construct is generated by gap fill, primer extension, or both.

[0210] In a 112thExample is the method of any one of Examples 93-97, 107, 108, and 111, wherein the di-tag molecule comprises a universal priming site derived from the recording tag, a compartment tag derived from the recording tag, a unique molecular identifier derived from the recording tag, an optional spacer derived from the recording tag, an encoder sequence derived from the coding tag, a unique molecular identifier derived from the coding tag, an optional spacer derived from the coding tag, and a universal priming site derived from the coding tag.

[0211] In a 113thExample is the method of any one of Examples 93-112, wherein the analyte and the associated recording tag are covalently joined to the solid support.

[0212] In a 114thExample is the method of Example 113, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducingelectronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0213] In a 115thExample is the method of Example 114, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0214] In a 116thExample is the method of any one of Examples 93-115, wherein the binding agent is a polypeptide or protein.

[0215] In a 117thExample is the method of Example 116, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or an antibody or binding fragment thereof.

[0216] In an 118thExample is the method of any one of Example 95-117 wherein the binding agent binds to a single amino acid residue, a dipeptide, a tripeptide or a post-translational modification of the peptide.

[0217] In a 119thExample is the method of Example 118, wherein the binding agent binds to an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue.

[0218] In a 120thExample is the method of Example 118, wherein the binding agent binds to an N-terminal peptide, a C-terminal peptide, or an internal peptide.

[0219] In a 121stExample is method of Example 119, wherein the binding agent binds to the N- terminal amino acid residue and the N-terminal amino acid residue is cleaved after each binding cycle.

[0220] In a 122ndExample is the method of Example 119, wherein the binding agent binds to the C-terminal amino acid residue and the C-terminal amino acid residue is cleaved after each binding cycle.

[0221] Example 123. The method of Example 121, wherein the N-terminal amino acid residue is cleaved via Edman degradation.

[0222] Example 124. The method of Example 93, wherein the binding agent is a site-specific covalent label of an amino acid or post-translational modification.

[0223] Example 125. The method of any one of Examples 93-124, wherein following step (b), complexes comprising the analyte and associated binding agents are dissociated from the solid support and partitioned into an emulsion of droplets or microfluidic droplets.

[0224] Example 126. The method of Example 125, wherein each microfluidic droplet, on average, comprises one complex comprising the analyte and the binding agents.

[0225] Example 127. The method of Example 125 or 126, wherein the recording tag is amplified prior to generating an extended coding tag or di-tag construct.

[0226] Example 128. The method of any one of Examples 125-127, wherein emulsion fusion PCR is used to transfer the recording tag information to the coding tag or to create a population of di-tag constructs.

[0227] Example 129. The method of any one of Examples 93-128, wherein the collection of extended coding tags or di-tag constructs are amplified prior to analysis.

[0228] Example 130. The method of any one of Examples 93-129, wherein analyzing the collection of extended coding tags or di-tag constructs comprises a nucleic acid sequencing method.

[0229] Example 131. The method of Example 130, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

[0230] Example 132. The method of Example 130, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0231] Example 133. The method of Example 130, wherein a partial composition of the analyte is determined by analysis of a plurality of extended coding tags or di-tag constructs using unique compartment tags and optionally UMIs.

[0232] Example 134. The method of any one of Examples 1-133, wherein the analysis step is performed with a sequencing method having a per base error rate of > 5%, > 10%, > 15%, > 20%, > 25%, or > 30%.

[0233] Example 135. The method of any one of Examples 1-134, wherein the identifying components of a coding tag, recording tag, or both comprise error correcting codes.

[0234] Example 136. The method of Example 135, wherein the identifying components are selected from an encoder sequence, barcode, UMI, compartment tag, cycle specific sequence, or any combination thereof.

[0235] Example 137. The method of Example 135 or 136, wherein the error correcting code is selected from Hamming code, Lee distance code, asymmetric Lee distance code, Reed-Solomon code, and Levenshtein-Tenengolts code.

[0236] Example 138. The method of any one of Examples 1-134, wherein the identifying components of a coding tag, recording tag, or both are capable of generating a unique current or ionic flux or optical signature, wherein the analysis step comprises detection of the unique current or ionic flux or optical signature in order to identify the identifying components.

[0237] Example 139. The method of Example 138, wherein the identifying components are selected from an encoder sequence, barcode, UMI, compartment tag, cycle specific sequence, or any combination thereof.

[0238] Example 140. A method for analyzing a plurality of analytes (e.g., molecules of the same analyte or of different analytes), comprising the steps of: (a) providing a plurality of analytes and associated recording tags joined to a solid support; (b) contacting the plurality of analytes with a plurality of binding agents capable of binding to cognate analytes, wherein each binding agent comprises a coding tag with identifying information regarding the binding agent; (c) transferring the information of a first coding tag of a first binding agent to a first recording tag associated with the first analyte to generate a first order extended recording tag, wherein the first binding agent binds to the first analyte; (d) contacting the plurality of analytes with the plurality of binding agents capable of binding to cognate analytes; (e) transferring the information of a second coding tag of a second binding agent to the first order extended recording tag to generate a second order extended recording tag, wherein the second binding agent binds to the first analyte; (f) optionally repeating steps (d) - (e) for "n" binding cycles, wherein the information of each coding tag of each binding agent that binds to the first analyte is transferred to the extended recording tag generated from the previous binding cycle to generate an rP1order extended recording tag that represents the first analyte; (g) analyzing the order extended recording tag.

[0239] Example 141. The method of Example 140, wherein a plurality of n order extended recording tags that represent a plurality of analytes are generated and analyzed.

[0240] Example 142. The method of Example 140 or 141, wherein the analyte is a protein.

[0241] Example 143. The method of Example 142, wherein the anlayte is a peptide.

[0242] Example 144. The method of Example 143, wherein the peptide is obtained by fragmenting proteins from a biological sample.

[0243] Example 145. The method of any one of Examples 140-144, wherein the plurality of analytes comprises analytes (e.g., macromolecules such as polypeptides, proteins, protein complexes) from multiple, pooled samples.

[0244] Example 146. The method of any one of Examples 140-145, wherein the recording tag is a DNA molecule, an RNA molecule, a PNA molecule, a BNA molecule, an XNA, molecule, an LNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0245] Example 147. The method of any one of Examples 140-146, wherein the recording tag comprises a unique molecular identifier (UMI).

[0246] Example 148. The method of Examples 140-147, wherein the recording tag comprises a compartment tag.

[0247] Example 149. The method of any one of Examples 140-148, wherein the recording tag comprises a universal priming site.

[0248] Example 150. The method of any one of Examples 140-149, wherein the recording tag comprises a spacer at its 3 '-terminus.

[0249] Example 151. The method of any one of Examples 140-150, wherein the coding tag comprises an encoder sequence.

[0250] Example 152. The method of any one of Examples 140-151, wherein the coding tag comprises a UMI.

[0251] Example 153. The method of any one of Examples 140-152, wherein the coding tag comprises a universal priming site.

[0252] Example 154. The method of any one of Examples 140-153, wherein the coding tag comprises a spacer at its 3 '-terminus.

[0253] Example 155. The method of any one of Examples 140-154, wherein the coding tag comprises a binding cycle specific sequence.

[0254] Example 156. The method of any one of Examples 140-155, wherein the coding tag comprises a unique molecular identifier.

[0255] Example 157. The method of any one of Examples 140-156, wherein the binding agent and the coding tag are joined by a linker.

[0256] Example 158. The method of any one of Examples 140-157, wherein transferring information of the recording tag to the coding tag is mediated by primer extension.

[0257] Example 159. The method of any one of Examples 140-158, wherein transferring information of the recording tag to the coding tag is mediated by ligation.

[0258] Example 160. The method of any one of Examples 140-159, wherein the plurality of analytes, the associated recording tags, or both are covalently joined to the solid support.

[0259] Example 161. The method of any one of Examples 140-160, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0260] Example 162. The method of Example 161, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0261] Example 163. The method of any one of Examples 140-162, wherein the binding agent is a polypeptide or protein.

[0262] Example 164. The method of Example 163, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or an antibody or binding fragment thereof.

[0263] Example 165. The method of any one of Examples 142-164 wherein the binding agent binds to a single amino acid residue, a dipeptide, a tripeptide or a post-translational modification of the peptide.

[0264] Example 166. The method of Example 165, wherein the binding agent binds to an N- terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue.

[0265] Example 167. The method of Example 165, wherein the binding agent binds to an N- terminal peptide, a C-terminal peptide, or an internal peptide.

[0266] Example 168. The method of any one of Examples 142-164, wherein the binding agent binds to a chemical label of a modified N-terminal amino acid residue, a modified C-terminal amino acid residue, or a modified internal amino acid residue.

[0267] Example 169. The method of Example 166 or 168, wherein the binding agent binds to the N-terminal amino acid residue or the chemical label of the modified N-terminal amino acid residue, and the N-terminal amino acid residue is cleaved after each binding cycle.

[0268] Example 170. The method of Example 166 or 168, wherein the binding agent binds to the C-terminal amino acid residue or the chemical label of the modified C-terminal amino acid residue, and the C-terminal amino acid residue is cleaved after each binding cycle.

[0269] Example 171. The method of Example 169, wherein the N-terminal amino acid residue is cleaved via Edman degradation, Edmanase, a modified aminopeptidase, or a modified acylpeptide hydrolase.

[0270] Example 172. The method of Example 163, wherein the binding agent is a site-specific covalent label of an amino acid or post-translational modification.

[0271] Example 173. The method of any one of Examples 140-172, wherein the plurality of nthorder extended recording tags are amplified prior to analysis.

[0272] Example 174. The method of any one of Examples 140-173, wherein analyzing the 77thorder extended recording tag comprises a nucleic acid sequencing method.

[0273] Example 175. The method of Example 174, wherein a plurality of nthorder extended recording tags representing a plurality of analytes are analyzed in parallel.

[0274] Example 176. The method of Example 174 or 175, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

[0275] Example 177. The method of Example 174 or 175, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0276] Example . A method, comprising: (a) contacting a set of proteins, wherein each protein is associated directly or indirectly with a recording tag, with a library of agents, wherein each agent comprises (i) a small molecule, a peptide or peptide mimetic, a peptidomimetic (e.g., a peptoid, a β-peptide, or a D-peptide peptidomimetic), a polysaccharide, or an aptamer (e.g., a nucleic acid aptamer, such as a DNA aptamer, or a peptide aptamer), and (ii) a coding tag comprising identifying information regarding the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer, wherein each protein and / or its associated recording tag, or each agent, is immobilized directly or indirectly to a support; (b) allowing transfer of information between (i) the recording tag associated with each protein that binds and / or reacts with the small molecule(s), peptide(s) or peptide mimetic(s), peptidomimetic(s) (e.g., peptoid(s), P-peptide(s), or D-peptide peptidomimetic(s)), polysaccharide(s), or aptamer(s) of one or more agents, and (ii) the coding tag of the one or more agents, to generate an extended recording tag and / or an extended coding tag; and (c) analyzing the extended recording tag and / or the extended coding tag.

[0277] Example 2' . The method of Example , wherein each protein is spaced apart from other proteins on the support at an average distance equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, equal to or greater than about 500 nm, equal to or greater than about 550 nm, equal to or greater than about 600 nm, equal to or greater than about 650 nm, equal to or greater than about 700 nm, equal to or greater than about 750 nm, equal to or greater than about 800 nm, equal to or greater than about 850 nm, equal to or greater than about 900 nm, equal to or greater than about 950 nm, or equal to or greater than about 1 μιη.

[0278] Example 3 ' . The method of Example or 2', wherein each protein and its associated recording tag is spaced apart from other proteins and their associated recording tags onthe support at an average distance equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, equal to or greater than about 500 nm, equal to or greater than about 550 nm, equal to or greater than about 600 nm, equal to or greater than about 650 nm, equal to or greater than about 700 nm, equal to or greater than about 750 nm, equal to or greater than about 800 nm, equal to or greater than about 850 nm, equal to or greater than about 900 nm, equal to or greater than about 950 nm, or equal to or greater than about 1 μιη.

[0279] Example 4' . The method of any one of Examples -3 ', wherein one or more of the proteins and / or their associated recording tags are covalently immobilized to the support (e.g., via a linker), or non-covalently immobilized to the support (e.g., via a binding pair).

[0280] Example 5' . The method of any one of Examples -4', wherein a subset of the proteins and / or their associated recording tags are covalently immobilized to the support while another subset of the proteins and / or their associated recording tags are non-covalently immobilized to the support.

[0281] Example 6' . The method of any one of Examples -5', wherein one or more of the recording tags are immobilized to the support, thereby immobilizing the associated protein(s).

[0282] Example 7' . The method of any one of Examples -6', wherein one or more of the proteins are immobilized to the support, thereby immobilizing the associated recording tag(s).

[0283] Example 8' . The method of any one of Examples 1-7, wherein at least one protein co-localizes with its associated recording tag, while each is independently immobilized to the support.

[0284] Example 9' . The method of any one of Examples -8', wherein at least one protein and / or its associated recording tag associates directly or indirectly with an immobilizing linker, and the immobilizing linker is immobilized directly or indirectly to the support, thereby immobilizing the at least one protein and / or its associated recording tag to the support.

[0285] Example 10' . The method of any one of Examples -9', wherein the density of immobilized recording tags is equal to or greater than the density of immobilized proteins.

[0286] Example 1 1 ' . The method of Example 10', wherein the density of immobilized recording tags is at least about 2-fold, at least about 3-fold, at least about 4-fold, at least about 5- fold, at least about 6-fold, at least about 7-fold, at least about 8-fold, at least about 9-fold, at least about 10-fold, at least about 20-fold, at least about 50-fold, at least about 100-fold, or more, of the density of immobilized proteins.

[0287] Example 12' . The method of Example , wherein each agent is spaced apart from other agents immobilized on the support at an average distance equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, equal to or greater than about 500 nm, equal to or greater than about 550 nm, equal to or greater than about 600 nm, equal to or greater than about 650 nm, equal to or greater than about 700 nm, equal to or greater than about 750 nm, equal to or greater than about 800 nm, equal to or greater than about 850 nm, equal to or greater than about 900 nm, equal to or greater than about 950 nm, or equal to or greater than about 1 μιη.

[0288] Example 13 ' . The method of Example 12', wherein one or more of the agents are covalently immobilized to the support (e.g., via a linker), or non-covalently immobilized to the support (e.g., via a binding pair).

[0289] Example 14' . The method of Example 12' or 13 ', wherein a subset of the agents are covalently immobilized to the support while another subset of the agents are non-covalently immobilized to the support.

[0290] Example 15' . The method of any one of Examples 12'-14', wherein for one or more of the agents, the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β- peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer is immobilized to the support, thereby immobilizing the coding tag.

[0291] Example 16' . The method of any one of Examples 12'-15', wherein for one or more of the agents, the coding tag is immobilized to the support, thereby immobilizing the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer.

[0292] Example 17' . The method of any one of Examples -16', wherein information is transferred from at least one coding tag to at least one recording tag, thereby generating at least one extended recording tag.

[0293] Example 18' . The method of any one of Examples -17', wherein information is transferred from at least one recording tag to at least one coding tag, thereby generating at least one extended coding tag.

[0294] Example 19' . The method of any one of Examples -18', wherein at least one di- tag construct is generated comprising information from the coding tag and information from the recording tag.

[0295] Example 20' . The method of any one of Examples -19', wherein at least one of the proteins binds and / or reacts with the small molecules, peptides or peptide mimetics,peptidomimetics (e.g., peptoids, β-peptides, or D-peptide peptidomimetics), polysaccharides, or aptamers of two or more agents.

[0296] Example 21 ' . The method of Example 20' , wherein the extended recording tag or the extended coding tag comprises identifying information regarding the small molecules, peptides or peptide mimetics, peptidomimetics (e.g., peptoids, β-peptides, or D-peptide peptidomimetics), polysaccharides, or aptamers of the two or more agents.

[0297] Example 22' . The method of any one of Examples 1 '-21 ', wherein at least one of the proteins is associated with two or more recording tags, wherein the two or more recording tags can be the same or different.

[0298] Example 23 ' . The method of any one of Examples -22', wherein at least one of the agents comprises two or more coding tags, wherein the two or more coding tags can be the same or different.

[0299] Example 24' . The method of any one of Examples -23 ', wherein the transfer of information is accomplished by ligation (e.g., an enzymatic or chemical ligation, a splint ligation, a sticky end ligation, a single-strand (ss) ligation such as a ssDNA ligation, or any combination thereof), a polymerase-mediated reaction (e.g., primer extension of single-stranded nucleic acid or double-stranded nucleic acid), or any combination thereof.

[0300] Example 25' . The method of Example 24', wherein the ligation and / or polymerase- mediated reaction have faster kinetics relative to the binding occupancy time or reaction time between the protein and the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer, optionally wherein a reagent for the ligation and / or polymerase-mediated reaction is present in the same reaction volume as the binding or reaction between the protein and the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer, and further optionally wherein information transfer is effected by using a concomitantbinding / encoding step, and / or by using a temperature of the encoding or information writing step that is decreased to slow the off rate of the binding agent.

[0301] Example 26' . The method of any one of Examples -25', wherein each protein associates with its recording tag via individual attachment, and / or wherein each small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer associates with its coding tag via individual attachment.

[0302] Example 27' . The method of Example 26', wherein the attachment occurs via ribosome or mRNA / cDNA display in which the recording tag and / or coding tag sequence information is contained in the mRNA sequence.

[0303] Example 28' . The method of Example 27', wherein the recording tag and / or coding tag comprise a universal primer sequence, a barcode, and / or a spacer sequence at the 3' end of the mRNA sequence.

[0304] Example 29' . The method of Example 28', wherein the recording tag and / or coding tag, at the 3' end, further comprise a restriction enzyme digestion site.

[0305] Example 30' . The method of any one of Examples -29', wherein the set of proteins is a proteome or subset thereof, optionally wherein the set of proteins are produced using in vitro transcription of a genome or subset thereof followed by in vitro translation, or produced using in vitro translation of a transcriptome or subset thereof.

[0306] Example 31 ' . The method of Example 30', wherein the subset of the proteome comprises a kinome; a secretome; a receptome (e.g., GPCRome); an immunoproteome; a nutriproteome; a proteome subset defined by a post-translational modification (e.g.,phosphorylation, ubiquitination, methylation, acetylation, glycosylation, oxidation, lipidation, and / or nitrosylation), such as a phosphoproteome (e.g., phosphotyrosine-proteome, tyrosine- kinome, and tyrosine-phosphatome), a glycoproteome, etc; a proteome subset associated with a tissue or organ, a developmental stage, or a physiological or pathological condition; a proteome subset associated a cellular process, such as cell cycle, differentiation (or de-differentiation), cell death, senescence, cell migration, transformation, or metastasis; or any combination thereof.

[0307] Example 32' . The method of any one of Examples -3 , wherein the set of proteins are from a mammal such as human, a non-human animal, a fish, an invertebrate, an arthropod, an insect, or a plant, e.g., a yeast, a bacterium, e.g., E. Coli, a virus, e.g., HIV or HCV, or a combination thereof.

[0308] Example 33' . The method of any one of Examples -32', wherein the set of proteins comprise a protein complex or subunit thereof.

[0309] Example 34' . The method of any one of Examples -33', wherein the recording tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0310] Example 35' . The method of any one of Examples -34', wherein the recording tag comprises a universal priming site.

[0311] Example 36' . The method of any one of Examples -35', wherein the recording tag comprises a priming site for amplification, sequencing, or both, for example, the universal priming site comprises a priming site for amplification, sequencing, or both.

[0312] Example 37' . The method of any one of Examples -36', wherein the recording tag comprises a unique molecule identifier (UMI).

[0313] Example 38' . The method of any one of Examples -37', wherein the recording tag comprises a barcode.

[0314] Example 39' . The method of any one of Examples -38', wherein the recording tag comprises a spacer at its 3 '-terminus.

[0315] Example 40' . The method of any one of Examples -39', wherein the support is a solid support, such as a rigid solid support, a flexible solid support, or a soft solid support, and including a porous support or a non-porous support.

[0316] Example 4 . The method of any one of Examples -40', wherein the support comprises a bead, a porous bead, a magnetic bead, a paramagnetic bead, a porous matrix, an array, a surface, a glass surface, a silicon surface, a plastic surface, a slide, a filter, nylon, a chip, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a well, a microtitre well, a plate, an ELISA plate, a disc, a spinning interferometry disc, a membrane, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle (e.g., comprising a metal such as magnetic nanoparticles (Fe304), gold nanoparticles, and / or silver nanoparticles), quantum dots, a nanoshell, a nanocage, a microsphere, or any combination thereof.

[0317] Example 42' . The method of Example 41 ', wherein the support comprises a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a magnetic bead, a paramagnetic bead, a glass bead, or a controlled pore bead, or any combination thereof.

[0318] Example 43 ' . The method of any one of Examples -42', which is for parallel analysis of the interaction between the set of proteins and the library of small molecules, and / or peptides or peptide mimetics, and / or peptidomimetics (e.g., peptoids, β-peptides, or D-peptide peptidomimetics), and / or polysaccharides, and / or aptamers, in order to create a small molecule- protein binding matrix, and / or a peptide / peptide mimetic-protein binding matrix, and / or a peptidomimetic-protein binding matrix (e.g., a peptoid-protein binding matrix, a β-peptide-protein binding matrix, or a D-peptide peptidomimetic-protein binding matrix), and / or a polysaccharide- protein binding matrix, and / or an aptamer-protein binding matrix.

[0319] Example 44' . The method of Example 43 ', wherein the matrix size is of about 102, about 103, about 104, about 105, about 106, about 107, about 108, about 109, about 1010, about 1011, about 1012, about 1013, about 1014, or more, for example, of about 2>< 1013.

[0320] Example 45' . The method of any one of Examples -44', wherein the coding tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNAwith pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0321] Example 46' . The method of any one of Examples -45', wherein the coding tag comprises an encoder sequence that identifies the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer.

[0322] Example 47' . The method of any one of Examples -46', wherein the coding tag comprises a spacer, a unique molecular identifier (UMI), a universal priming site, or anycombination thereof.

[0323] Example 48' . The method of any one of Examples -47', wherein the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer and the coding tag are joined by a linker or a binding pair.

[0324] Example 49' . The method of any one of Examples -48', wherein the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer and the coding tag are joined by a SpyTag- KTag / SpyLigase (where two moieties to be joined have the SpyTag / KTag pair, and the SpyLigase joins Spy Tag to KTag, thus joining the two moieties), a Spy Tag / Spy Catcher, aSnoopTag / SnoopCatcher peptide-protein pair, a sortase, or a HaloTag / HaloTag ligand pair, or any combination thereof.

[0325] Example 50' . A method for analyzing a polypeptide, comprising: (a) contacting (i) a set of fragments of a polypeptide, wherein each fragment is associated directly or indirectly with a recording tag, with (ii) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding tag comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent, and wherein each fragment and / or its associated recording tag, or each binding agent, is immobilized directly or indirectly to a support; (b) allowing transfer of information between (i) the recording tag associated with each fragment and (ii) the coding tag, upon binding between the binding moiety and the one or more N-terminal, internal, orC-terminal amino acids of the fragment, to generate an extended recording tag and / or an extended coding tag; and (c) analyzing the extended recording tag and / or the extended coding tag.

[0326] Example 51 ' . The method of Example 50' , wherein the one or more N-terminal, internal, or C-terminal amino acids comprise: (i) an N-terminal amino acid (NTAA); (ii) an N- terminal dipeptide sequence; (iii) an N-terminal tripeptide sequence; (iv) an internal amino acid; (v) an internal dipeptide sequence; (vi) an internal tripeptide sequence; (vii) a C-terminal amino acid (CTAA); (viii) a C-terminal dipeptide sequence; or (ix) a C-terminal tripeptide sequence, or any combination thereof, optionally wherein any one or more of the amino acid residues in (i)-(ix) are modified or functionalized.

[0327] Example 52' . The method of Example 51 ' , wherein the one or more N-terminal, internal, or C-terminal amino acids are selected, independently at each residue, from the group consisting of Alanine (A or Ala), Cysteine (C or Cys), Aspartic Acid (D or Asp), Glutamic Acid (E or Glu), Phenylalanine (F or Phe), Glycine (G or Gly), Histidine (H or His), Isoleucine (I or He), Lysine (K or Lys), Leucine (L or Leu), Methionine (M or Met), Asparagine (N or Asn), Proline (P or Pro), Glutamine (Q or Gin), Arginine (R or Arg), Serine (S or Ser), Threonine (T or Thr), Valine (V or Val), Tryptophan (W or Trp), and Tyrosine (Y or Tyr), in any combination thereof.

[0328] Example 53' . The method of any one of Examples 50' -52', wherein the binding moiety comprises a polypeptide or fragment thereof, a protein or polypeptide chain or fragment thereof, or a protein complex or subunit thereof, such as an antibody or antigen binding fragment thereof.

[0329] Example 54' . The method of any one of Examples 50' -53', wherein the binding moiety comprises an anticalin or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS or variant, mutant, or modified protein thereof; a UBR box protein or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or any combination thereof.

[0330] Example 55' . The method of any one of Examples 50'-54', wherein the binding moiety is capable of selectively and / or specifically binding to a functionalized N-terminal aminoacid (NTAA), an N-terminal dipeptide sequence, or an N-terminal tripeptide sequence, or any combination thereof.

[0331] Example 56' . A method for analyzing a plurality of polypeptides, comprising: (a) labeling each molecule of a plurality of polypeptides with a plurality of universal tags; (b) contacting the plurality of polypeptides with a plurality of compartment tags, under a condition suitable for annealing or joining of the plurality of universal tags with the plurality of compartment tags, thereby partitioning the plurality of polypeptides into a plurality of compartments (e.g., a bead surface, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof), wherein the plurality of compartment tags are the same within each compartment and are different from the compartment tags of other compartments; (c) fragmenting the polypeptide(s) in each compartment, thereby generating a set of polypeptide fragments each associated with a recording tag comprising at least one universal polynucleotide tag and at least one compartment tag; (d) immobilizing the set of polypeptide fragments, directly or indirectly, to a support; (e) contacting the immobilized set of polypeptide fragments with a library of binding agents, wherein each binding agent comprises a binding moiety and a coding tag comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N- terminal, internal, or C-terminal amino acids modified by a functionalizing reagent; (f) allowing transfer of information between (i) the recording tag associated with each fragment and (ii) the coding tag, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of the fragment, to generate an extended recording tag and / or an extended coding tag; and (g) analyzing the extended recording tag and / or the extended coding tag.

[0332] Example 57' . The method of Example 56', wherein the plurality of polypeptides with the same compartment tag belong to the same protein.

[0333] Example 58' . The method of Example 56', wherein the plurality of polypeptides with the same compartment tag belong to different proteins, for example, two, three, four, five, six, seven, eight, nine, ten, or more proteins.

[0334] Example 59' . The method of any one of Examples 56'-58', wherein the plurality of compartment tags are immobilized to a plurality of substrates, with each substrate defining a compartment.

[0335] Example 60' . The method of Example 59', wherein the plurality of substrates are selected from the group consisting of a bead, a porous bead, a magnetic bead, a paramagnetic bead, a porous matrix, an array, a surface, a glass surface, a silicon surface, a plastic surface, a slide, a filter, nylon, a chip, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a well, a microtitre well, a plate, an ELISA plate, a disc, a spinning interferometry disc, a membrane, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle (e.g., comprising a metal such as magnetic nanoparticles (Fe304), gold nanoparticles, and / or silver nanoparticles), quantum dots, a nanoshell, a nanocage, a microsphere, or any combination thereof.

[0336] Example 61 ' . The method of Example 59' or 60', wherein each of the plurality of substrates comprises a bar-coded particle, such as a bar-coded bead, e.g., a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a magnetic bead, a paramagnetic bead, a glass bead, or a controlled pore bead, or any combination thereof.

[0337] Example 62' . The method of any one of Examples 59'-6 , wherein the support is selected from the group consisting of a bead, a porous bead, a magnetic bead, a paramagnetic bead, a porous matrix, an array, a surface, a glass surface, a silicon surface, a plastic surface, a slide, a filter, nylon, a chip, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a well, a microtitre well, a plate, an ELISA plate, a disc, a spinning interferometry disc, a membrane, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle (e.g., comprising a metal such as magnetic nanoparticles (Fe304), gold nanoparticles, and / or silver nanoparticles), quantum dots, a nanoshell, a nanocage, a microsphere, or any combination thereof.

[0338] Example 63' . The method of Example 62', wherein the support comprises a sequencing bead, e.g., a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a magnetic bead, a paramagnetic bead, a glass bead, or a controlled pore bead, or any combination thereof.

[0339] Example 64' . The method of any one of Examples 56' -63', wherein each fragment and its associated recording tag is spaced apart from other fragments and their associated recordingtags on the support at an average distance equal to or greater than about 20 nm, equal to or greater than about 50 nm, equal to or greater than about 100 nm, equal to or greater than about 150 nm, equal to or greater than about 200 nm, equal to or greater than about 250 nm, equal to or greater than about 300 nm, equal to or greater than about 350 nm, equal to or greater than about 400 nm, equal to or greater than about 450 nm, equal to or greater than about 500 nm, equal to or greater than about 550 nm, equal to or greater than about 600 nm, equal to or greater than about 650 nm, equal to or greater than about 700 nm, equal to or greater than about 750 nm, equal to or greater than about 800 nm, equal to or greater than about 850 nm, equal to or greater than about 900 nm, equal to or greater than about 950 nm, or equal to or greater than about 1 μιη.

[0340] Example 65' . A method for analyzing a plurality of polypeptides, comprising: (a) immobilizing a plurality of polypeptides to a plurality of substrates, wherein each substrate comprises a plurality of recording tags each comprising a compartment tag, optionally wherein each compartment is a bead, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof; (b) fragmenting (e.g., by a protease digestion) the polypeptide(s) immobilized on each substrate, thereby generating a set of polypeptide fragments immobilized to the substrate; (c) contacting the immobilized set of polypeptide fragments with a library of binding agents, wherein each binding agent comprises a binding moiety and a coding tag comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent; (d) allowing transfer of information between (i) the recording tag and (ii) the coding tag, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of each fragment, to generate an extended recording tag and / or an extended coding tag; and (e) analyzing the extended recording tag and / or the extended coding tag.

[0341] Example 66' . The method of Example 65', wherein the plurality of polypeptides with the same compartment tag belong to the same protein.

[0342] Example 67' . The method of Example 65', wherein the plurality of polypeptides with the same compartment tag belong to different proteins, for example, two, three, four, five, six, seven, eight, nine, ten, or more proteins.

[0343] Example 68' . The method of any one of Examples 65'-67', wherein each substrate defines a compartment.

[0344] Example 69' . The method of any one of Examples 65'-68', wherein the plurality of substrates are selected from the group consisting of a bead, a porous bead, a porous matrix, an array, a surface, a glass surface, a silicon surface, a plastic surface, a slide, a filter, nylon, a chip, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a well, a microtitre well, a plate, an ELISA plate, a disc, a spinning interferometry disc, a membrane, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle (e.g., comprising a metal such as magnetic nanoparticles (Fe304), gold nanoparticles, and / or silver nanoparticles), quantum dots, a nanoshell, a nanocage, a microsphere, or any combination thereof.

[0345] Example 70' . The method of any one of Examples 65'-69', wherein each of the plurality of substrates comprises a bar-coded particle, such as a bar-coded bead, e.g., a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a magnetic bead, a paramagnetic bead, a glass bead, or a controlled pore bead, or any combination thereof.

[0346] Example 71 ' . The method of any one of Examples 50'-70', wherein thefunctionalizing reagent comprises a chemical agent, an enzyme, and / or a biological agent, such as an isothiocyanate derivative, 2,4-dinitrobenzenesulfonic (D BS), 4-sulfonyl-2-nitrofluorobenzene (SNFB) l-fluoro-2,4-dinitrobenzene, dansyl chloride, 7-methoxycoumarin acetic acid, athioacylation reagent, a thioacetylation reagent, or a thiobenzylation reagent.

[0347] Example 72' . The method of any one of Examples 50'-7Γ, wherein the recording tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0348] Example 73' . The method of any one of Examples 50' -72', wherein the recording tag comprises a universal priming site; a priming site for amplification, sequencing, or both;optionally, a unique molecule identifier (UMI); a barcode; optionally, a spacer at its 3 '-terminus; or a combination thereof.

[0349] Example 74' . The method of any one of Examples 50' -73', which is for determining the sequence(s) of the polypeptide or plurality of polypeptides.

[0350] Example 75' . The method of any one of Examples 50'-74', wherein the coding tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino, or a combination thereof.

[0351] Example 76' . The method of any one of Examples 50'-75', wherein the coding tag comprises an encoder sequence, an optional spacer, an optional unique molecular identifier (UMI), a universal priming site, or any combination thereof.

[0352] Example 77' . The method of any one of Examples 50'-76', wherein the binding moiety and the coding tag are joined by a linker or a binding pair.

[0353] Example 78' . The method of any one of Examples 50'-77', wherein the binding moiety and the coding tag are joined by a SpyTag-KTag / SpyLigase (where two moieties to be joined have the SpyTag / KTag pair, and the Spy Ligase joins Spy Tag to KTag, thus joining the two moieties), a SpyTag / SpyCatcher, a SnoopTag / SnoopCatcher peptide-protein pair, a sortase, or a HaloTag / HaloTag ligand pair, or any combination thereof.

[0354] Example 79' . The method of any one of Examples -78', wherein the coding tag and / or the recording tag comprise one or more error correcting codes, one or more encoder sequences, one or more barcodes, one or more UMIs, one or more compartment tags, or any combination thereof.

[0355] Example 80' . The method of Example 79', wherein the error correcting code is selected from Hamming code, Lee distance code, asymmetric Lee distance code, Reed-Solomon code, and Levenshtein-Tenengolts code.

[0356] Example 81 ' . The method of any one of Examples -80', wherein analyzing the extended recording tag and / or extended coding tag comprises a nucleic acid sequence analysis.

[0357] Example 82' . The method of Example 8 , wherein the nucleic acid sequence analysis comprises a nucleic acid sequencing method, such as sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing, or any combination thereof.

[0358] Example 83 ' . The method of Example 82', wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0359] Example 84' . The method of any one of Examples -83 ', further comprising one or more washing steps.

[0360] Example 85' . The method of any one of Examples -84', wherein the extended recording tag and / or extended coding tag are amplified prior to analysis.

[0361] Example 86' . The method of any one of Examples -85', wherein the extended recording tag and / or extended coding tag undergo a target enrichment assay prior to analysis.

[0362] Example 87' . The method of any one of Examples -86', wherein the extended recording tag and / or extended coding tag undergo a subtraction assay prior to analysis.

[0363] In one aspect, disclosed herein is a kit, comprising: (a) a library of agents, wherein each agent comprises (i) a small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β- peptide, or D-peptide peptidomimetic), polysaccharide, and / or aptamer, and (ii) a coding tag comprising identifying information regarding the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer; and optionally (b) a set of proteins, wherein each protein is associated directly or indirectly with a recording tag, wherein each protein and / or its associated recording tag, or each agent, isimmobilized directly or indirectly to a support, and wherein the set of proteins, the recording tags, and the library of agents are configured to allow information transfer between (i) the recording tag associated with each protein that binds and / or reacts with the small molecule(s), peptide(s) or peptide mimetic(s), peptidomimetic(s) (e.g., peptoid(s), P-peptide(s), or D-peptidepeptidomimetic(s)), polysaccharide(s), or aptamer(s) of one or more agents, and (ii) the coding tag of the one or more agents, to generate an extended recording tag and / or an extended coding tag.

[0364] In one aspect, disclosed herein is a kit for analyzing a polypeptide, comprising: (a) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding tag comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modifiedby a functionalizing reagent; and optionally (b) a set of fragments of a polypeptide, wherein each fragment is associated directly or indirectly with a recording tag, or (b') a means for fragmenting a polypeptide, such as a protease, wherein each fragment and / or its associated recording tag, or each binding agent, is immobilized directly or indirectly to a support, and wherein the set of fragments of a polypeptide, the recording tags, and the library of binding agents are configured to allow transfer of information between (i) the recording tag associated with each fragment and (ii) the coding tag, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of the fragment, to generate an extended recording tag and / or an extended coding tag.

[0365] In one aspect, disclosed herein is a kit for analyzing a plurality of polypeptides, comprising: (a) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding tag comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent; and (b) a plurality of substrates, optionally with a plurality of polypeptides immobilized thereto, wherein each substrate comprises a plurality of recording tags each comprising a compartment tag, optionally wherein each compartment is a bead, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof, wherein the polypeptide(s) immobilized on each substrate are configured to be fragmented (e.g., by a protease cleavage) to generate a set of polypeptide fragments immobilized to the substrate, wherein the plurality of polypeptides, the recording tags, and the library of binding agents are configured to allow transfer of information between (i) the recording tag and (ii) the coding tag, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of each fragment, to generate an extended recording tag and / or an extended coding tag.

[0366] The following aspects provide additional illustrations of the present disclosure.

[0367] Aspect 1. A method for analyzing a polypeptide, comprising the steps of: (a) providing the polypeptide optionally associated directly or indirectly with a recording tag; (b) functionalizing the N-terminal amino acid (NTAA) of the polypeptide with a chemical reagent, wherein the chemical reagent comprises a compound selected from the group consisting of (i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; andoptionally wherein when R3isR1ancj R2ARE NO^ JJ. (ii) a compound of Formula (II):*H(Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)Rg, or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5N=C=S (Hi)or a salt or conjugate thereof,whereinis Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^1, -S(0)2Rj, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula (IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, NR13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH,(c) contacting the polypeptide with a first binding agent comprising a first binding portion capable of binding to the functionalized NTAA and(cl) a first coding tag with identifying information regarding the first binding agent, or (c2) a first detectable label;(d) (dl) transferring the information of the first coding tag to the recording tag to generate an extended recording tag and analyzing the extended recording tag, or(d2) detecting the first detectable label;wherein step (b) is conducted before step (c), after step (c) and before step (d), or after step (d).

[0368] In some embodiments, this method of sequencing employs an "Edman-like" N-terminal amino acid degradation process. Edman-like degradation consists of two key steps: 1)Functionalization of the□ -amine on the NTAA of the peptide, and 2) Elimination of the functionalized NTAA. Standard Edman functionalization chemistry as well as the Edman-like functionalization chemistry described herein exhibits poorer functionalization and elimination of N- terminal proline residues. As such, the presence of an N-terminal proline may lead to "stalling" of the cyclic sequencing reaction. Thus, in some embodiments of the methods described herein, it is beneficial to remove any N-terminal prolines at the start of each Edman-like degradation cycle by exposing the target polypeptide to a proline aminopeptidase (proline iminopeptidase) which specifically cleaves just N terminal prolines. Accordingly, in some embodiments, each of the methods and assays described herein can optionally include an additional step of contacting the polypeptide being analyzed with a proline aminopeptidase. Likewise, kits for performing these methods can, optionally, include at least one proline aminopeptidase.

[0369] There are several proline aminopeptidases (PAPs) known in the literature that can be used for this purpose. In a preferred embodiment, small monomelic PAPs (-25-35 kDa) are employed for removal of NTAA prolines. Suitable monomelic PAPs for use in the methods and kits described herein include family members from B. coagulans, L. delbrueckii, N. gonorrhoeae, F. meningosepticum, S. marcescens, T. acidophilum, and L. plantarum (MEROPS S33.001)(Nakajima, Ito et al. 2006) (Kitazono, Yoshimoto et al. 1992). Suitable multimeric PAPs are also known, and include enzyme from D hansenii (Bolumar, Sanz et al. 2003). Either native or engineered PAPs may be employed. Effective mapping of peptide sequences generated by the methods and assays herein that are devoid of proline residues can be accomplished by mapping peptide reads back to a "proline minus" proteome. At the bioinformatic level, this essentially translates to proteins comprised of 19 amino acid residues rather than 20.

[0370] Alternatively, to retain proline information, two steps of binding can be employed both before and after proline removal to enable detection of proline residues, but this comes at the extra cost of an extra binding / encoding cycle for each sequencing cycle. Furthermore, this concept of combining Edman-like chemistry with R-group specific aminopeptidases can be used to remove anyNTF / NTE recalcitrant amino acid; however, in the preferred embodiments, only a single recalcitrant amino residue, typically proline, is removed by an aminopeptidase. Removal of multiple residues leads to a combinatoric explosion of removed sequences (i.e. removal of P and W leads to removal of sequences with runs of Ps, runs of Ws, and runs of P and W.)

[0371] Aspect 2. The method of Aspect 1, wherein step (a) comprises providing the polypeptide and an associated recording tag joined to a support (e.g., a solid support).

[0372] Aspect 3. The method of Aspect 1, wherein step (a) comprises providing the polypeptide joined to an associated recording tag in a solution.

[0373] Aspect 4. The method of Aspect 1, wherein step (a) comprises providing the polypeptide associated indirectly with a recording tag.

[0374] Aspect 5. The method of Aspect 1, wherein the polypeptide is not associated with a recording tag in step (a).

[0375] Aspect 6. The method of any one of Aspects 1-5, wherein step (b) is conducted before step (c).

[0376] Aspect 7. The method of any one of Aspects 1-5, wherein step (b) is conducted after step (c) and before step (d).

[0377] Aspect 8. The method of any one of Aspects 1-5, wherein step (b) is conducted after both step (c) and step (d).

[0378] Aspect 9. The method of any one of Aspects 1-5, wherein steps (a), (b), (cl), and (dl) occur in sequential order.

[0379] Aspect 10. The method of any one of Aspects 1-5, wherein steps (a), (cl), (b), and (dl) occur in sequential order.

[0380] Aspect 11. The method of any one of Aspects 1-5, wherein steps (a), (cl), (dl), and (b) occur in sequential order.

[0381] Aspect 12. The method of any one of Aspects 1-5, wherein steps (a), (b), (c2), and (d2) occur in sequential order.

[0382] Aspect 13. The method of any one of Aspects 1-5, wherein steps (a), (c2), (b), and (d2) occur in sequential order.

[0383] Aspect 14. The method of any one of Aspects 1-5, wherein steps (a), (c2), (d2), and (b) occur in sequential order.

[0384] Aspect 15. The method of any one of Aspects 1-14, wherein step (c) further comprises contacting the polypeptide with a second (or higher order) binding agent comprising a second (or higher order) binding portion capable of binding to a functionalized NTAA other than the functionalized NTAA of step (b) and a coding tag with identifying information regarding the second (or higher order) binding agent.

[0385] Aspect 16. The method of Aspect 15, wherein contacting the polypeptide with the second (or higher order) binding agent occurs in sequential order following the polypeptide being contacted with the first binding agent.

[0386] Aspect 17. The method of Aspect 15, wherein contacting the polypeptide with the second (or higher order) binding agent occurs simultaneously with the polypeptide being contacted with the first binding agent.

[0387] Aspect 18. A method for analyzing a polypeptide, comprising the steps of:(a) providing the polypeptide optionally associated directly or indirectly with a recording tag;(b) functionalizing the N-terminal amino acid (NTAA) of the polypeptide with a chemical reagent to yield a functionalized NTAA, wherein the chemical reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):R2 JL^N^R3H (I)or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; and optionally wherein when R3isR1ancj R2are noJJ. (ii) a compound of Formor a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)Rg, or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (III)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula (IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted; and(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl; and(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; anda compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, R13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH,(c) contacting the polypeptide with a first binding agent comprising a first binding portion capable of binding to the functionalized NTAA and (cl) a first coding tag with identifying information regarding the first binding agent, or (c2) a first detectable label;(d) (dl) transferring the information of the first coding tag to the recording tag to generate a first extended recording tag and analyzing the extended recording tag, or(d2) detecting the first detectable label, and(e) eliminating the functionalized NTAA to expose a new NTAA;wherein step (b) is conducted before step (c), after step (c) and before step (d), or after step (d).

[0388] In some embodiments of the compound of Formula (I) for use in any of the methods and kits disclosed herein, R3is a monocyclic heteroaryl group. In some embodiments of Formula (I), R3is a 5- or 6-membered monocyclic heteroaryl group. In some embodiments of Formula (I), R3is a 5- or 6-membered monocyclic heteroaryl group containing one or more N. Preferably, R3is selected from pyrazole, imidazole, triazole and tetrazole, and is linked to the amidine of Formula (I) via a nitrogen atom of the pyrazole, imidazole, triazole or tetrazole ring, and R3is optionallysubstituted by a group selected from halo, C1-3 alkyl, C1-3 haloalkyl, and nitro. In someembodiments, R3isΝ¾ / , wherein Gi is N, CH, or CX where X is halo, C1-3 alkyl, C1-3haloalkyl, or nitro. In some embodiments, R3is N¾or ?where X is Me, F, CI, CF3, or NO2. InI G-i i N some embodiments, R is N¾s?wherein Gi is N or CH. In some embodiments, R isNc¾ / .In some embodiments, R3is a bicyclic heteroaryl group. In some embodiments, R3is a 9- or 10-membered bicyclic heteroaryl group. In some embodiments, R3isor

[0389] Aspect 19. The method of Aspect 18, wherein step (a) comprises providing the polypeptide and an associated recording tag joined to a support (e.g., a solid support).

[0390] Aspect 20. The method of Aspect 18, wherein step (a) comprises providing the polypeptide joined to an associated recording tag in a solution.

[0391] Aspect 21. The method of Aspect 18, wherein step (a) comprises providing the polypeptide associated indirectly with a recording tag.

[0392] Aspect 22. The method of Aspect 18, wherein the polypeptide is not associated with a recording tag in step (a).

[0393] Aspect 23. The method of any one of Aspects 18-22, wherein step (b) is conducted before step (c).

[0394] Aspect 24. The method of any one of Aspects 18-22, wherein step (b) is conducted after step (c) and before step (d).

[0395] Aspect 25. The method of any one of Aspects 18-22, wherein step (b) is conducted after both step (c) and step (d).

[0396] Aspect 26. The method of any one of Aspects 18-22, wherein steps (a), (b), (cl), and (dl) occur in sequential order.

[0397] Aspect 27. The method of any one of Aspects 18-22, wherein steps (a), (cl), (b), and (dl) occur in sequential order.

[0398] Aspect 28. The method of any one of Aspects 18-22, wherein steps (a), (cl), (dl), and (b) occur in sequential order.

[0399] Aspect 29. The method of any one of Aspects 18-22, wherein steps (a), (b), (c2), and (d2) occur in sequential order.

[0400] Aspect 30. The method of any one of Aspects 18-22, wherein steps (a), (c2), (b), and (d2) occur in sequential order.

[0401] Aspect 31. The method of any one of Aspects 18-22, wherein steps (a), (c2), (d2), and (b) occur in sequential order.

[0402] Aspect 32. The method of any one of Aspects 18-31, further comprising the steps of:(f) functionalizing the new NTAA of the polypeptide with a chemical reagent to yield a newly functionalized NTAA;(g) contacting the polypeptide with a second (or higher order) binding agent comprising a second (or higher order) binding portion capable of binding to the newly functionalized NTAA and (gl) a second coding tag with identifying information regarding the second (or higher order) binding agent, or (g2) a second detectable label;(h) (hi) transferring the information of the second coding tag to the first extended recording tag to generate a second extended recording tag and analyzing the second extended recording tag, or(h2) detecting the second detectable label, and(i) eliminating the functionalized NTAA to expose a new NTAA;wherein step (f) is conducted before step (g), after step (g) and before step (h), or after step(h).

[0403] In any of the aspects 1-32, the method optionally further includes a step of contacting the polypeptide with a proline aminopeptidase, typically before the recited method steps, under conditions suitable to cleave any N-terminal proline present.

[0404] Aspect 33. The method of Aspect 32, wherein the chemical reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; and optionally wherein when R3is N¾¾ / ?R1ancj R2are not both H;(ii) a compound of Formula (II):* H (II)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (III)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocycl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted; and(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl; anda metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):(VII)or a salt or conjugate thereof,whereinG1is N, NR13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH.

[0405] Aspect 34. The method of Aspect 32 or Aspect 33, wherein step (f) is conducted before step (g).

[0406] Aspect 35. The method of Aspect 32 or Aspect 33, wherein step (f) is conducted after step (g) and before step (h).

[0407] Aspect 36. The method of Aspect 32 or Aspect 33, wherein step (f) is conducted after both step (g) and step (h).

[0408] Aspect 37. The method of Aspect 32 or Aspect 33, wherein steps (f), (gl), and (hi) occur in sequential order.

[0409] Aspect 38. The method of Aspect 32 or Aspect 33, wherein steps (gl), (f), and (hi) occur in sequential order.

[0410] Aspect 39. The method of Aspect 32 or Aspect 33, wherein steps (gl), (hi), and (f) occur in sequential order.

[0411] Aspect 40. The method of Aspect 32 or Aspect 33, wherein steps (f), (g2), and (h2) occur in sequential order.

[0412] Aspect 41. The method of Aspect 32 or Aspect 33, wherein steps (g2), (f), and (h2) occur in sequential order.

[0413] Aspect 42. The method of Aspect 32 or Aspect 33, wherein steps (g2), (h2), and (f) occur in sequential order.

[0414] Aspect 43. The method of any one of Aspects 32-42, wherein contacting the polypeptide with the second (or higher order) binding agent occurs in sequential order following the polypeptide being contacted with the first binding agent.

[0415] Aspect 44. The method of any one of Aspects 32-42, wherein contacting the polypeptide with the second (or higher order) binding agent occurs simultaneously with the polypeptide being contacted with the first binding agent.

[0416] Aspect 45. The method of any one of Aspects 1-44, wherein the polypeptide is obtained by fragmenting a protein from a biological sample.

[0417] Aspect 46. The method of any one of Aspects 1-45, wherein the recording tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo-complementary bases, a DNA with protected bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino DNA, or a combination thereof.

[0418] Aspect 47. The method of Aspect 46, wherein the DNA molecule is backbone modified, sugar modified, or nucleobase modified.

[0419] Aspect 48. The method of Aspect 46, wherein the DNA molecule has nucleobase protecting groups such as Alloc, electrophilic protecting groups such as thiaranes, acetyl protecting groups, nitrobenzyl protecting groups, sulfonate protecting groups, or traditional base-labile protecting groups including Ultramild reagents.

[0420] Aspect 49. The method of any one of Aspects 1-48, wherein the recording tag comprises a universal priming site.

[0421] Aspect 50. The method of Aspect 49, wherein the universal priming site comprises a priming site for amplification, sequencing, or both.

[0422] Aspect 51. The method of Aspects 1-50, where the recording tag comprises a unique molecule identifier (UMI).

[0423] Aspect 52. The method of any one of Aspects 1-51, wherein the recording tag comprises a barcode.

[0424] Aspect 53. The method of any one of Aspects 1-52, wherein the recording tag comprises a spacer at its 3 '-terminus.

[0425] Aspect 54. The method of Aspect any one of Aspects 1-53, wherein the polypeptide and the associated recording tag are covalently joined to the support.

[0426] Aspect 55. The method of any one of Aspects 1-54, wherein the support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0427] Aspect 56. The method of Aspect 55, wherein the support comprises gold, silver, a semiconductor or quantum dots.

[0428] Aspect 57. The method of Aspect 55, wherein the nanoparticle comprises gold, silver, or quantum dots.

[0429] Aspect 58. The method of Aspect 55, wherein the support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, aparamagnetic bead, glass bead, or a controlled pore bead.

[0430] Aspect 59. The method of any one of Aspects 1-58, wherein a plurality of polypeptides and associated recording tags are joined to a support.

[0431] Aspect 60. The method of Aspect 59, wherein the plurality of polypeptides are spaced apart on the support, wherein the average distance between the polypeptides is about > 20 nm.

[0432] Aspect 61. The method of any one of Aspects 1-60, wherein the binding portion of the binding agent comprises a peptide or protein.

[0433] Aspect 62. The method of any one of Aspects 1-61, wherein the binding portion of the binding agent comprises an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS (such as ClpS2) or variant, mutant, or modified protein thereof; a UBR box protein or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or an antibody or binding fragment thereof; or any combination thereof.

[0434] Aspect 63. The method of any one of Aspects 1-62, wherein the binding agent binds to a single amino acid residue (e.g., an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue), a dipeptide (e.g., an N-terminal dipeptide, a C-terminal dipeptide, or an internal dipeptide), a tripeptide (e.g., an N-terminal tripeptide, a C-terminal tripeptide, or an internal tripeptide), or a post-translational modification of the polypeptide.

[0435] Aspect 64. The method of any one of Aspects 1-62, wherein the binding agent binds to a NTAA-functionalized single amino acid residue, a NTAA-functionalized dipeptide, a NTAA- functionalized tripeptide, or a NTAA-functionalized polypeptide.

[0436] Aspect 65. The method of any one of Aspects 1-64, wherein the binding portion of the binding agent is capable of selectively binding to the polypeptide.

[0437] Aspect 66. The method of any one of Aspects 1-65, wherein the coding tag is DNA molecule, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0438] Aspect 67. The method of any one of Aspects 1-66, wherein the coding tag comprises an encoder or barcode sequence.

[0439] Aspect 68. The method of any one of Aspects 1-67, wherein the coding tag further comprises a spacer, a binding cycle specific sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0440] Aspect 69. The method of any one of Aspects 1-68, wherein the binding portion and the coding tag are joined by a linker.

[0441] Aspect 70. The method of Aspects 1-69, wherein the binding portion and the coding tag are joined by a SpyTag / SpyCatcher peptide-protein pair, a SnoopTag / SnoopCatcher peptide-protein pair, or a HaloTag / HaloTag ligand pair.

[0442] Aspect 71. The method of any one of Aspects 1-70, wherein transferring the information of the coding tag to the recording tag is mediated by a DNA ligase or an RNA ligase.

[0443] Aspect 72. The method of any one of Aspects 1-70, wherein transferring the information of the coding tag to the recording tag is mediated by a DNA polymerase, an RNA polymerase, or a reverse transcriptase.

[0444] Aspect 73. The method of any one of Aspects 1-70, wherein transferring the information of the coding tag to the recording tag is mediated by chemical ligation.

[0445] Aspect 74. The method of Aspect 73, wherein the chemical ligation is performed using single-stranded DNA.

[0446] 75. The method of Aspect 74, wherein the chemical ligation is performed using double- stranded DNA.

[0447] 76. The method of any one of Aspects 1-72, wherein analyzing the extended recording tag comprises a nucleic acid sequencing method.

[0448] 77. The method of Aspect 76, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

[0449] 78. The method of Aspect 76, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0450] 79. The method of any one of Aspects 1-78, wherein the extended recording tag is amplified prior to analysis

[0451] 80. The method of any one of Aspects 1-79, further comprising the step of adding a cycle label.

[0452] 81. The method of Aspect 80, wherein the cycle label provides information regarding the order of binding by the binding agents to the polypeptide.

[0453] 82. The method of Aspect 80 or Aspect 81, wherein the cycle label is added to the coding tag.

[0454] 83. The method of Aspect 80 or Aspect 81, wherein the cycle label is added to the recording tag.

[0455] 84. The method of Aspect 80 or Aspect 81, wherein the cycle label is added to the binding agent.

[0456] 85. The method of Aspect 80 or Aspect 81, wherein the cycle label is added independent of the coding tag, recording tab, and binding agent.

[0457] 86. The method of any one of Aspects 1-85, wherein the order of coding tag information contained on the extended recording tag provides information regarding the order of binding by the binding agents to the polypeptide.

[0458] 87. The method of any one of Aspects 1-86, wherein frequency of the coding tag information contained on the extended recording tag provides information regarding the frequency of binding by the binding agents to the polypeptide.

[0459] 88. The method of any one of Aspects 1-87, wherein a plurality of extended recording tags representing a plurality of polypeptides is analyzed in parallel.

[0460] 89. The method of Aspect 88, wherein the plurality of extended recording tags representing a plurality of polypeptides is analyzed in a multiplexed assay.

[0461] 90. The method of Aspect 88 or 89, wherein the plurality of extended recording tags undergoes a target enrichment assay prior to analysis.

[0462] 91. The method of any one of Aspects 88-90, wherein the plurality of extended recording tags undergoes a subtraction assay prior to analysis.

[0463] 92. The method of any one of Aspects 88-91, wherein the plurality of extended recording tags undergoes a normalization assay to reduce highly abundant species prior to analysis.

[0464] 93. The method of any one of Aspects 1-92, wherein the NT A A is eliminated by chemical cleavage or enzymatic cleavage from the polypeptide.

[0465] 94. The method of Aspect 93, wherein the NTAA is eliminated by a carboxypeptidase or aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; mild Edman degradation; Edmanase enzyme; TFA, a base; or any combination thereof.

[0466] 95. The method of Aspect 94, wherein the mild Edman degradation uses a dichloro or monochloro acid

[0467] 96. The method of Aspect 94, wherein the mild Edman degradation uses TFA, TCA, or DCA.

[0468] 97. The method of Aspect 94, wherein the mild Edman degradation usestriethylammonium acetate (Et3NHOAc).

[0469] 98. The method of Aspect 94, wherein the base is a hydroxide, an alkylated amine, a cyclic amine, a carbonate buffer, or a metal salt.

[0470] 99. The method of Aspect 98, wherein the hydroxide is sodium hydroxide

[0471] 100. The method of Aspect 98, wherein the alkylated amine is selected from methylamine, ethylamine, propylamine, dimethylamine, diethylamine, dipropylamine,trimethylamine, triethylamine, tripropylamine, cyclohexylamine, benzylamine, aniline,diphenylamine, Ν,Ν-Diisopropylethylamine (DIPEA), and lithium diisopropylamide (LDA).

[0472] 101. The method of Aspect98, wherein the cyclic amine is selected from pyridine, pyrimidine, imidazole, pyrrole, indole, piperidine, prolidine, l,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and l,5-diazabicyclo[4.3.0]non-5-ene (DBN).

[0473] 102. The method of Aspect 98, wherein the carbonate buffer comprises sodium carbonate, potassium carbonate, calcium carbonate, sodium bicarbonate, potassium bicarbonate, or calcium bicarbonate.

[0474] 103. The method of Aspect 98, wherein the metal salt comprises silver.

[0475] 104. The method of Aspect 103, wherein the metal salt is AgClC .

[0476] 105. The method of any one of Aspects 1-104, wherein at least one binding agent binds to a terminal amino acid residue, terminal di-amino-acid residues, or terminal tri-amino-acid residues.

[0477] 106. The method of any one of Aspects 1-105, wherein at least one binding agent binds to a post-translationally modified amino acid.

[0478] 107. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the grou consisting of a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; and optionally wherein when R3isR1ancj R2are not both H.

[0479] 108. The method of Aspect 107, wherein R1i is

[0480] 109. The method of Aspect 107 or 108, whereinR2i is

[0481] 110. The method of any one of Aspects 107-109, wherein R or R is

[0482] 111. The method of any one of Aspects 107-110, wherein R3isN;¾ / , wherein0483] 112. The method of any one of Aspects 107-110, wherein R is or

[0484] 113. The method of Aspect 107, wherein the compound of Formula (I) is selectedfrom the group consisting of, and optionally further including a compound selected from the following(N-Boc,N'-trifluoroacetyl-pyrazolecarboxamidine, Ν,Ν'-bisacetyl-pyrazolecarboxamidine, N- methyl-pyrazolecarboxamidine, N,N'-bisacetyl-N-methyl-pyrazolecarboxamidine, N,N'-bisacetyl- N-methyl-4-nitro-pyrazolecarboxamidine, and N,N'-bisacetyl-N-methyl-4-trifluoromethyl- pyrazolecarboxamidine), or a salt or conjugate thereof.

[0485] 114 The method of any one of Aspects 107-113, wherein the chemical reagent additionally comprises Mukaiyama' s reagent (2-chloro-l-methylpyridinium iodide).

[0486] 115. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the roup consisting of a compound of Formula (II):H (Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted.

[0487] 116. The method of Aspect 115, wherein R4is carboxybenzyl.

[0488] 117. The method of Aspect 115, wherein R4is -C(0)R and R is C2-6alkenyl, optionally substituted with aryl, heteroaryl, or heterocycloalkyl.

[0489] 118. The method of Aspect 115, wherein the compound is selected from the groupnsisting ofor a salt or conjugate thereof.

[0490] 119. The method of any one of Aspects 115-118, wherein the chemical reagent additionally comprises TMS-C1, Sc(OTf)2, Zn (OTf)2, or a lanthanide-containing reagent.

[0491] 120. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (III):R5N=C=S (in)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^1, -S(0)2Ri, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted.

[0492] 121. The method of Aspect 120, wherein R5is substituted phenyl.

[0493] 122. The method of Aspect 120 or Aspect 121, wherein R5is phenyl, substituted with one or more groups selected from the group consisting of halo, -NR^R1, -S(0)2Ri, and heterocyclyl.

[0494] 123. The method of Aspect 120, wherein the compound of Formula (III) is trimethylsilyl isothiocyanate (TMSITC) or pentafluorophenyl isothiocyanate (PFPITC).

[0495] 124. The method of any one of Aspects 120-123, wherein the chemical reagent additionally comprises a carbodiimide compound.

[0496] 125. The method of any one of Aspects 120-124, wherein the NTAA is eliminated using trifluoroacetic acid or hydrochloric acid.

[0497] 126. The method of any one of Aspects 120-124, wherein the NTAA is eliminated using mild Edman degradation.

[0498] 127. The method of any one of Aspects 120-124, wherein the NTAA is eliminated using Edmanase or an engineered hydrolase, aminopeptidase, or carboxypeptidase.

[0499] 128. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (IV):R6R C^N'(iv)or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted.

[0500] 129. The method of Aspect 128, wherein R6and R7are each independently H, Ci-6alkyl or cycloalkyl.

[0501] 130. The method of Aspect 128, wherein the compound is selected from the groupor conjugate thereof.

[0502] 131. The method of any one of Aspects 128-130, wherein the compound of Formula (IV) is prepared by desulfurization of the corresponding thiourea.

[0503] 132. The method of any one of Aspects 128-131, wherein the chemical reagent additionally comprises Mukaiyama' s reagent (2-chloro-l-methylpyridinium iodide).

[0504] 133. The method of any one of Aspects 128-131, wherein the chemical reagent additionally comprises a Lewis acid.

[0505] 134. The method of Aspect 133, wherein the Lewis acid selected from N- ((aryl)imino-acenapthenone)ZnCl2, Zn(OTf)2, ZnCh, PdCh, CuCl, and CuCh.

[0506] 135. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (V):OR9^R8(V)or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl.

[0507] 136. The method of Aspect 135, wherein R8is chloro.

[0508] 137. The method of Aspect 135 or Aspect 136, wherein R9is hydrogen or bromo.

[0509] 138. The method of any one of Aspects 135-137, wherein the chemical reagent additionally comprises a peptide coupling reagent.

[0510] 139. The method of Aspect 138, wherein the peptide coupling reagent is a carbodiimide compound.

[0511] 140. The method of Aspect 139, wherein the carbodiimide compound is diisopropylcarbodiimide (DIC) or l-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC).

[0512] 141. The method of any one of Aspects 135-140, wherein the NTAA is eliminated using acylpeptide hydrolase (APH).

[0513] 142. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different.

[0514] 143. The method of Aspect 142, wherein M is Co.

[0515] 144. The method of Aspect 142 or Aspect 143, wherein the chemical reagent comprises a czs- ^hydroxyaquo(triethylenetetramine)cobalt(III) complex.

[0516] 145. The method of Aspect 142, wherein the chemical reagent comprises β- [Co(trien)(OH)(OH2)]2+.

[0517] 146. The method of any one of Aspects 1-106, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, R13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH.

[0518] 147. The method of Aspect 146, wherein G1is CH2and G2is CH or G1is NH andG2iis N.

[0519] 148 The method of Aspect 146 or 147, wherein R12is H.

[0520] 149 The method of any one of Aspects 146-148, wherein R10and R11are each H.

[0521] 150 The method of Aspect 146, wherein the compound of Formula (VII) isselected from the group consisting of, and , or a salt or conjugate thereof.

[0522] 151. The method of any one of Aspects 107-150, wherein the NTAA is eliminated using a base.

[0523] 152. The method of Aspect 151, wherein the base is a hydroxide, an alkylated amine, a cyclic amine, a carbonate buffer, or a metal salt.

[0524] 153. The method of Aspect 152, wherein the hydroxide is sodium hydroxide.

[0525] 154. The method of Aspect 152, wherein the alkylated amine is selected from methylamine, ethylamine, propylamine, dimethylamine, diethylamine, dipropylamine,trimethylamine, triethylamine, tripropylamine, cyclohexylamine, benzylamine, aniline,diphenylamine, Ν,Ν-diisopropylethylamine (DIPEA), and lithium diisopropylamide (LDA).

[0526] 155. The method of Aspect 152, wherein the cyclic amine is selected from pyridine, pyrimidine, imidazole, pyrrole, indole, piperidine, proolidine, 1,8- diazabicyclo[5.4.0]undec-7-ene (DBU), and l,5-diazabicyclo[4.3.0]non-5-ene (DBN).

[0527] 156. The method of Aspect 152, wherein the carbonate buffer comprises sodium carbonate, potassium carbonate, calcium carbonate, sodium bicarbonate, potassium bicarbonate, or calcium bicarbonate.

[0528] 157. The method of Aspect 152, wherein the metal salt comprises silver.

[0529] 158. The method of Aspect 152, wherein the metal salt is AgClC .

[0530] 159. The method of any one of Aspects 1-158, wherein the chemical reagent comprises a conjugate selected from the group consisting of / Formula (I)-Q, wherein R1, R2, and R3are as defined for Formula (I) in Aspect 1 , and Q is a ligand;Formula (II)-Q,wherein R4is as defined for For a ligand;wherein R5is as defined for For a ligand;wherein R6and R7are as defined for Formula (IV) in Aspect 1 , and Q is a ligand;a (V)-Q,wherein R8and R9are as defined for Formula (V) in Aspect 1, and Q is a ligand;(MLn)-Q Formula (VI)-Q, wherein M, L, and n are as defined for Formula (VI) in Aspect 1, and Q is a ligand;R11OR12 P / Formula (VII)-Q,wherein R10, R11, R12, R15, G1, G2, and p are as defined for Formula (VII) in Aspect 1, and Q is a ligand.

[0531] 160. The method of Aspect 159, wherein the Q is selected from the group consisting of -Ci-6alkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, heterocyclyl, -N=C=S, - CN, -C(0)Rn, -C(0)OR°, -SRpor -S(0)2Rq; wherein the -Ci-ealkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, and heterocyclyl are each unsubstituted or substituted, and Rn, R°, Rp, and Rqare each independently selected from the group consisting of -Ci-6alkyl, -Ci-6haloalkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, and heterocyclyl.

[0532] 161. The method of Aspect 159, wherein the Q is selected from the groupconsisting of

[0533] 162. The method of Aspect 159, wherein Q is a fluorophore.

[0534] 163. The method of any one of Aspects 1-162, wherein step (b) of Aspect 1 or Aspect 5 comprises difunctionalization of the NTAA.

[0535] 164. The method of Aspect 163, wherein step (b) of Aspect 1 or Aspect 5 comprises difunctionalizing the NTAA with (1) a first chemical reagent comprising a compound selected from the group consisting of a compound of Formula (I), (II), (III), (IV), (V), (VI), and (VII), or a salt or conjugate thereof, and (2) a second chemical reagent .

[0536] 165. The method of Aspect 164, wherein the second chemical reagent comprises a compound of Formula (Villa) or (Vlllb):0^R3(Villa) or a salt or conjugate thereof,whereinR13is H, Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, wherein the Ci-6alkyl, aryl, heteroaryl, cycloalkyl, and heterocycloalkyl are each unsubstituted or substituted; orR13— X (VHIb)whereinR13is Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, each of which is unsubstituted or substituted; andX is a halogen.

[0537] 166. The method of 164 or 165, wherein step (b) of Aspect 1 or Aspect 5 comprises functionalizing the NTAA with the second chemical reagent prior to functionalizing with the first chemical reagent.

[0538] 167. The method of 164 or 165, wherein step (b) of Aspect 1 or Aspect 5 comprises functionalizing the NTAA with the first chemical reagent prior to functionalizing with the second chemical reagent.

[0539] 168. The method of any one of Aspects 32-167, wherein step (f) of Aspect 6 comprises difunctionalization of the NTAA.

[0540] 169. The method of Aspect 168, wherein the step (f) of Aspect 6 comprises difunctionalizing the NTAA with (1) a first chemical reagent comprising a compound selected from the group consisting of a compound of Formula (I), (II), (III), (IV), (V), (VI), and (VII) and (2) a second chemical reagent.

[0541] 170. The method of Aspect 169, wherein the second chemical reagent comprises a compound of Formula (Villa) or (VHIb):O^ 13R (Villa) or a salt or conjugate thereof,whereinR13is H, Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, wherein the Ci-6alkyl, aryl, heteroaryl, cycloalkyl, and heterocycloalkyl are each unsubstituted or substituted; orR13-X (villb)whereinR13is Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, each of which is unsubstituted or substituted; andX is a halogen.

[0542] 171. The method of 169 or 170, wherein step (b) of Aspect 1 or Aspect 5 comprises functionalizing the NTAA with the second chemical reagent prior to functionalizing with the first chemical reagent.

[0543] 172. The method of 169 or 170, wherein step (b) of Aspect 1 or Aspect 5 comprises functionalizing the NTAA with the first chemical reagent prior to functionalizing with the second chemical reagent.

[0544] 173. The method of any one of Aspects 165-167 and 170-172, wherein the compound of Formula (Villa) is formaldehyde.

[0545] 174. The method of any one of Aspects 165-167 and 170-172, wherein the compound of Formula (Villb) is methyl iodide.

[0546] 175. A method for analyzing one or more polypeptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising:(a) partitioning the plurality of protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags optionally joined to a support (e.g., a solid support), wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments;(b) fragmenting the plurality of protein complexes, proteins, and / or polypeptides into a plurality of polypeptides;(c) contacting the plurality of polypeptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of polypeptides with the pluralityof compartment tags within the plurality of compartments, thereby generating a plurality of compartment tagged polypeptides;(d) collecting the compartment tagged polypeptides from the plurality of compartments; and(e) analyzing one or more compartment tagged polypeptide according to a method of any one of Aspects 1-174.

[0547] 176. The method of Aspect 175, wherein the compartment is a microfluidic droplet.

[0548] 177. The method of Aspect 175, wherein the compartment is a microwell.

[0549] 178. The method of Aspect 175, wherein the compartment is a separated region on a surface.

[0550] 179. The method of any one of Aspects 175-178, wherein each compartment comprises on average a single cell.

[0551] 180. A method for analyzing one or more polypeptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising:(a) labeling of the plurality of protein complexes, proteins, or polypeptides with a plurality of universal DNA tags;(b) partitioning the plurality of labeled protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags, wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments;(c) contacting the plurality of protein complexes, proteins, or polypeptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of protein complexes, proteins, or polypeptides with the plurality of compartment tags within the plurality of compartments, thereby generating a plurality of compartment tagged protein complexes, proteins or polypeptides;(d) collecting the compartment tagged protein complexes, proteins, or polypeptides from the plurality of compartments;(e) optionally fragmenting the compartment tagged protein complexes, proteins, or polypeptides into a compartment tagged polypeptides; and(f) analyzing one or more compartment tagged polypeptide according to a method of any one of Aspects 1-174.

[0552] 181. The method of any one of Aspects 175-180, wherein compartment tag information is transferred to a recording tag associated with a polypeptide via primer extension or ligation.

[0553] 182. The method of any one of Aspectsl75-181, wherein the support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0554] 183. The method of any one of Aspects 175-181, wherein the support comprises a bead.

[0555] 184. The method of Aspect 183, wherein the bead is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0556] 185. The method of any one of Aspects 175-184, wherein the compartment tag comprises a single stranded or double stranded nucleic acid molecule.

[0557] 186. The method of any one of Aspects 175-185, wherein the compartment tag comprises a barcode and optionally a UMI.

[0558] 187. The method of Aspect 186, wherein the support is a bead and thecompartment tag comprises a barcode, further wherein beads comprising the plurality ofcompartment tags joined thereto are formed by split-and-pool synthesis.

[0559] 188. The method of Aspect 186, wherein the support is a bead and thecompartment tag comprises a barcode, further wherein beads comprising a plurality of compartment tags joined thereto are formed by individual synthesis or immobilization.

[0560] 189. The method of any one of Aspects 175-188, wherein the compartment tag is a component within a recording tag, wherein the recording tag optionally further comprises a spacer,a barcode sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0561] 190. The method of any one of Aspects 175-189, wherein the compartment tags further comprise a functional moiety capable of reacting with an internal amino acid, the peptide backbone, or N-terminal amino acid on the plurality of protein complexes, proteins, or polypeptides.

[0562] 191. The method of Aspect 190, wherein the functional moiety is an aldehyde, an azide / alkyne, or a maleimide / thiol, or an epoxide / nucleophile, or an inverse electron demand Diels- Alder (iEDDA) group.

[0563] 192. The method of Aspect 190, wherein the functional moiety is an aldehyde group.

[0564] 193. The method of any one of Aspects 175-192, wherein the plurality of compartment tags is formed by: printing, spotting, ink-jetting the compartment tags into the compartment, or a combination thereof.

[0565] 194. The method of any one of Aspects 175-193, wherein the compartment tag further comprises a polypeptide.

[0566] 195. The method of Aspect 194, wherein the compartment tag polypeptide comprises a protein ligase recognition sequence.

[0567] 196. The method of Aspect 195, wherein the protein ligase is butelase I or a homolog thereof.

[0568] 197. The method of any one of Aspects 175-196, wherein the plurality of polypeptides is fragmented with a protease.

[0569] 198. The method of Aspect 197, wherein the protease is a metalloprotease.

[0570] 199. The method of Aspect 198, wherein the activity of the metalloprotease is modulated by photo-activated release of metallic cations.

[0571] 200. The method of any one of Aspects 175-199, further comprising subtraction of one or more abundant proteins from the sample prior to partitioning the plurality of polypeptides into the plurality of compartments.

[0572] 201. The method of Aspect 175-200, further comprising releasing the compartment tags from the support prior to joining of the plurality of polypeptides with the compartment tags.

[0573] 202. The method of Aspect 175, further comprising following step (d), joining the compartment tagged polypeptides to a support in association with recording tags.

[0574] 203. The method of Aspect 202, further comprising transferring information of the compartment tag on the compartment tagged polypeptide to the associated recording tag.

[0575] 204. The method of Aspect 203, further comprising removing the compartment tags from the compartment tagged polypeptides prior to step (e).

[0576] 205. The method of any one of Aspects 175-204, further comprising determining the identity of the single cell from which the analyzed polypeptide derived based on the analyzed polypeptide's compartment tag sequence.

[0577] 206. The method of any one of Aspects 175-204, further comprising determining the identity of the protein or protein complex from which the analyzed polypeptide derived based on the analyzed polypeptide's compartment tag sequence.

[0578] 207. The method of any one of Aspects 32-206, wherein steps (f), (g), (h), and (i) are repeated with multiple amino acids.

[0579] 208. The method of Aspect 207, wherein steps (f), (g), (h), and (i) are repeated with two or more amino acids.

[0580] 209. The method of Aspect 207, wherein steps (f), (g), and (h) are repeated with up to about 100 amino acids.

[0581] 210. A kit for analyzing a polypeptide, comprising:(a) a reagent for providing the polypeptide optionally associated directly or indirectly with a recording tag;(b) a reagent for functionalizing the N-terminal amino acid (NTAA) of the polypeptide, wherein the reagent comprises a compound selected from the group consisting of:(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; and optionally wherein when R3isR1ancj R2are not both H; (ii) a compound of Formuor a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (III)or a salt or conjugate thereof,whereinis Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^1, -S(0)2Rj, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula (IV):R6R~N '° (IV)or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):OR9^R8(V)or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, NR13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH;(c) a first binding agent comprising a first binding portion capable of binding to the functionalized NTAA and (cl) a first coding tag with identifying information regarding the first binding agent, or (c2) a first detectable label; and(d) a reagent for transferring the information of the first coding tag to the recording tag to generate an extended recording tag; and optionally(e) a reagent for analyzing the extended recording tag or a reagent for detecting the first detectable label.

[0582] 211. The kit of Aspect 210, wherein the reagent of (a) is configured to provide the polypeptide and an associated recording tag joined to a support (e.g., a solid support).

[0583] 212. The kit of Aspect 210, wherein the reagent of (a) is configured to provide the polypeptide associated directly with a recording tag in a solution.

[0584] 213. The kit of Aspect 210, wherein the reagent of (a) is configured to provide the polypeptide associated indirectly with a recording tag.

[0585] 214. The kit of Aspect 210, wherein the reagent of (a) is configured to provide the polypeptide which is not associated with a recording tag.

[0586] 215. The kit of any one of Aspects 210-214, wherein the kit comprises two or more different reagents for functionalizing the NTAA of the polypeptide.

[0587] 216. The kit of Aspect 215, wherein the kit comprises a first reagent comprising a compound selected from the group consisting of a compound of Formula (I), (II), (III), (IV), (V), (VI), and (VII), or a salt or conjugate thereof, as described in Aspect 125, and a second reagent.

[0588] 217. The kit of Aspect 216, wherein the second reagent comprises a compound of Formula (Villa) or (VHIb):O^ R 13 (Villa) or a salt or conjugate thereof,whereinR13is H, Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, wherein the Ci-6alkyl, aryl, heteroaryl, cycloalkyl, and heterocycloalkyl are each unsubstituted or substituted; orR13-X (villb)whereinR13is Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, each of which is unsubstituted or substituted; andX is a halogen.

[0589] 218. The kit of Aspect 217, wherein the compound of Formula (Villa) is formaldehyde.

[0590] 219. The kit of Aspect 217, wherein the compound of Formula (VHIb) is methyl iodide.

[0591] 220. The kit of any one of Aspects 210-219, wherein the kit comprises two or more different binding agents.

[0592] 221. The kit of any one of Aspects 210-220, further comprising a reagent for eliminating the functionalized NTAA to expose a new NTAA.

[0593] 222. The kit of any one of Aspects 211-221, wherein the kit comprises two or more different reagents for eliminating the functionalized NTAA.

[0594] 223. The kit of Aspect 221 or Aspect 222, wherein the reagent for eliminating the functionalized NTAA comprises a chemical cleavage reagent or an enzymatic cleavage reagent.

[0595] 224. The kit of Aspect 221 or Aspect 222, wherein the reagent for eliminating the functionalized NTAA comprises a carboxypeptidase or aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; a mild Edman degradation reagent; an Edmanase enzyme; TFA; a base; or any combination thereof.

[0596] 225. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (I):2RlNH (I)or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, -NRdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;RD, RE, and RFare each independently H or Ci-6alkyl; andoptionally wherein when R3is N¾¾ / ?R1ancj R2are not both H;.

[0597] 226. The kit of Aspect 225, wherein R .·s

[0598] 227. The kit of Aspect 225 or Aspect 226,whereiinnR2is.

[0599] 228. The kit of any one of Aspects 225-227, wherein R or R

[0600] 229. The kit of any one of Aspects 225-228, wherein R3isN :=1, wherein Gi is N or CH.30. The kit of any one of Aspects 225-228, wherein R3is0r

[0602] 231. The kit of Aspect 225, wherein the compound of Formula (I) is selected fromconjugate thereof.

[0603] 232. The kit of any one of Aspects 225-231, wherein the chemical reagent additionally comprises Mukaiyama' s reagent (2-chloro-l-methylpyridinium iodide).

[0604] 233. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (II):•.NR4AH (Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted.

[0605] 234. The kit of Aspect 142, wherein R4is carboxybenzyl.

[0606] 235. The kit of Aspect 142, wherein R4is -C(0)R and R is C2-6alkenyl, optionally substituted with aryl, heteroaryl, or heterocycloalkyl.

[0607] 236. The kit of Aspect 142, wherein the compound is selected from the groupnsisting ofor a salt or conjugate thereof.

[0608] 237. The kit of any one of Aspects 142-145, wherein the chemical reagent additionally comprises TMS-C1, Sc(OTf)2, Zn (OTf)2, or a lanthanide-containing reagent.

[0609] 238. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (III):R5N=C=S (in)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^1, -S(0)2Ri, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted.

[0610] 239. The kit of Aspect 238, wherein R5is substituted phenyl.

[0611] 240. The kit of Aspect 238 or Aspect 239, wherein R5is phenyl, substituted with one or more groups selected from the group consisting of halo, -NR^R1, -S(0)2Ri, and heterocyclyl.

[0612] 241. The kit of Aspect 238, wherein the compound of Formula (III) is trimethylsilyl isothiocyanate (TMSITC) or pentafluorophenyl isothiocyanate (PFPITC).

[0613] 242. The kit of any one of Aspects 238-240, wherein the chemical reagent additionally comprises a carbodiimide compound.

[0614] 243. The kit of any one of Aspects 238-242, wherein the reagent for eliminating the functionalized NTAA comprises trifluoroacetic acid or hydrochloric acid.

[0615] 244. The kit of any one of Aspects 238-243, wherein the reagent for eliminating the functionalized NTAA comprises a mild Edman degradation reagent.

[0616] 245. The kit of any one of Aspects 238-243, wherein the reagent for eliminating the functionalized NTAA comprises an Edmanase or an engineered hydrolase, aminopeptidase, or carboxypeptidase.

[0617] 246. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (IV):R6RVC(IV)or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted.

[0618] 247. The kit of Aspect 246 wherein R6and R7are each independently H, Ci-ealkyl or cycloalkyl.

[0619] 248. The kit of Aspect 246, wherein the compound is selected from the group consisting of

[0620] 249. The kit of any one of Aspects 246-248, wherein the compound of Formula (IV) is prepared by desulfurization of the corresponding thiourea.

[0621] 250. The kit of any one of Aspects 246-249, wherein the chemical reagent additionally comprises Mukaiyama' s reagent (2-chloro-l-methylpyridinium iodide).

[0622] 251. The kit of any one of Aspects 246-249, wherein the chemical reagent additionally comprises a Lewis acid.

[0623] 252. The kit of Aspect 251, wherein the Lewis acid selected from N-((aryl)imino- acenapthenone)ZnCl2, Zn(OTf)2, ZnCl2, PdCl2, CuCl, and CuCl2.

[0624] 253. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (V):OR9^R8(V)or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl.

[0625] 254. The kit of Aspect 253, wherein R8is chloro.

[0626] 255. The kit of Aspect 253 or Aspect 254, wherein R9is hydrogen or bromo.

[0627] 256. The kit of any one of Aspects 253-255, wherein the chemical reagent additionally comprises a peptide coupling reagent.

[0628] 257. The kit of Aspect 256, wherein the peptide coupling reagent is a carbodiimide compound.

[0629] 258. The kit of Aspect 257, wherein the carbodiimide compound isdiisopropylcarbodiimide (DIC) or l-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC).

[0630] 259. The kit of any one of Aspects 253-258, wherein the reagent for eliminating the functionalized NTAA comprises acylpeptide hydrolase (APH).

[0631] 260. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different.

[0632] 261. The kit of Aspect 260, wherein M is Co.

[0633] 262. The kit of Aspect 260 or 261, wherein the chemical reagent comprises a cis- β-hy droxy aquo(tri ethyl enetetramine)cob alt(III) compl ex .

[0634] 263. The kit of Aspect 260 or 261, wherein the chemical reagent comprises β- [Co(trien)(OH)(OH2)]2+.

[0635] 264. The kit of any one of Aspects 210-224, wherein the chemical reagent comprises a compound selected from the group consisting of a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, R13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH.

[0636] 265. The kit of Aspect 264, wherein G1is CH2and G2is CH or G1is NH and G2isN.

[0637] 266 The kit of Aspect 264 or 265, wherein R12is H.

[0638] 267 The kit of any one of Aspects 264-266, wherein R10and R11are each H.selected

[0640] 269. The kit of any one of Aspects 225-268, wherein the reagent for eliminating the functionalized NTAA comprises a base.

[0641] 270. The kit of Aspect 269, wherein the base is a hydroxide, an alkylated amine, a cyclic amine, a carbonate buffer, or a metal salt.

[0642] 271. The kit of Aspect 270, wherein the hydroxide is sodium hydroxide.

[0643] 272. The kit of Aspect 270, wherein the alkylated amine is selected from methylamine, ethylamine, propylamine, dimethylamine, diethylamine, dipropylamine,trimethylamine, triethylamine, tripropylamine, cyclohexylamine, benzylamine, aniline,diphenylamine, Ν,Ν-diisopropylethylamine (DIPEA), and lithium diisopropylamide (LDA).

[0644] 273. The kit of Aspect 270, wherein the cyclic amine is selected from pyridine, pyrimidine, imidazole, pyrrole, indole, piped dine, proolidine, l,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and l,5-diazabicyclo[4.3.0]non-5-ene (DBN).

[0645] 274. The kit of Aspect 270, wherein the carbonate buffer comprises sodium carbonate, potassium carbonate, calcium carbonate, sodium bicarbonate, potassium bicarbonate, or calcium bicarbonate.

[0646] 275. The kit of Aspect 270, wherein the metal salt comprises silver.

[0647] 276. The kit of Aspect 270, wherein the metal salt is AgClC .

[0648] 277. The kit of any one of Aspects 210-276, wherein the chemical reagent comprises a conjugate selected from the group consisting of / Formula (I)-Q, wherein R1, R2, and R3are as defined for Formula (I) in Aspect 1, and Q is a ligand;Formula (II)-Q,wherein R4is as defined for For a ligand;wherein R5is as defined for For ligand;wherein R6and R7are as defined for Formula (IV) in Aspect 1, and Q is a ligand;a (V)-Q,wherein R8and R9are as defined for Formula (V) in Aspect 1, and Q is a ligand;(MLn)-Q Formula (VI)-Q, wherein M, L, and n are as defined for Formula (VI) in Aspect 1, and Q is a ligand;R11OR12 P / Formula (VII)-Q,wherein R10, R11, R12, R15, G1, G2, and p are as defined for Formula (VII) in Aspect 1, and Q is a ligand.

[0649] 278. The kit of Aspect 277, wherein the Q is selected from the group consisting of -Ci-6alkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, heterocyclyl, -N=C=S, - CN, -C(0)Rn, -C(0)OR°, -SRpor -S(0)2Rq; wherein the -Ci-ealkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, and heterocyclyl are each unsubstituted or substituted, and Rn, R°, Rp, and Rqare each independently selected from the group consisting of -Ci-6alkyl, -Ci-6haloalkyl, -C2-6alkenyl, -C2-6alkynyl, aryl, heteroaryl, and heterocyclyl.

[0650] 279. The kit of Aspect 277, wherein the Q is selected from the group consisting of

[0651] 280. The kit of Aspect 277, wherein Q is a fluorophore.

[0652] 281. The kit of any one of Aspects 210-280, wherein the binding agent binds to a terminal amino acid residue, terminal di-amino-acid residues, or terminal tri-amino-acid residues.

[0653] 282. The kit of any one of Aspects 210-280, wherein the binding agent binds to a post-translationally modified amino acid.

[0654] 283. The kit of any one of Aspects 210-282, wherein the recording tag comprises a nucleic acid, an oligonucleotide, a modified oligonucleotide, a DNA molecule, a DNA with pseudo- complementary bases, a DNA with protected bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a morpholino DNA, or a combination thereof.

[0655] 284. The kit of Aspect 283, wherein the DNA molecule is backbone modified, sugar modified, or nucleobase modified.

[0656] 285. The kit of Aspect 283, wherein the DNA molecule has nucleobase protecting groups such as Alloc, electrophilic protecting groups such as thiranes, acetyl protecting groups, nitrobenzyl protecting groups, sulfonate protecting groups, or traditional base-labile protecting groups including Ultramild reagents.

[0657] 286. The kit of any one of Aspects 210-285, wherein the recording tag comprises a universal priming site.

[0658] 287. The kit of Aspect 286, wherein the universal priming site comprises a priming site for amplification, sequencing, or both.

[0659] 288. The kit of any one of Aspects 210-287, where the recording tag comprises a unique molecule identifier (UMI).

[0660] 289. The kit of any one of Aspects 210-288, wherein the recording tag comprises a barcode.

[0661] 290. The kit of any one of Aspects 210-288, wherein the recording tag comprises a spacer at its 3 '-terminus.

[0662] 291. The kit of any one of Aspects 210-290, wherein the reagents for providing the polypeptide and an associated recording tag joined to a support provide for covalent linkage of the polypeptide and the associated recording tag on the support.

[0663] 292. The kit of any one of Aspects 210-291, wherein the support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere

[0664] 293. The kit of Aspect 292, wherein the support comprises gold, silver, a semiconductor or quantum dots.

[0665] 294. The kit of Aspect 292, wherein the nanoparticle comprises gold, silver, or quantum dots.

[0666] 295. The kit of Aspect 292, wherein the support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0667] 296. The kit of any one of Aspects 210-295, wherein the reagents for providing the polypeptide and an associated recording tag joined to a support provide for a plurality of polypeptides and associated recording tags that are joined to a support.

[0668] 297. The kit of Aspect 296, wherein the plurality of polypeptides are spaced apart on the support, wherein the average distance between the polypeptides is about > 20 nm.

[0669] 298. The kit of any one of Aspects 210-297, wherein the binding agent is a peptide or protein.

[0670] 299. The kit of any one of Aspects 210-298, wherein the binding agent comprises an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or an antibody or binding fragment thereof; or any combination thereof.

[0671] 300. The kit of any one of Aspects 210-299, wherein the binding agent binds to a single amino acid residue {e.g., an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue), a dipeptide {e.g., an N-terminal dipeptide, a C-terminal dipeptide, or an internal dipeptide), a tripeptide {e.g., an N-terminal tripeptide, a C-terminal tripeptide, or an internal tripeptide), or a post-translational modification of the analyte or polypeptide.

[0672] 301. The kit of any one of Aspects 210-300, wherein the binding agent binds to a NTAA-functionalized single amino acid residue, a NTAA-functionalized dipeptide, a NTAA- functionalized tripeptide, or a NTAA-functionalized polypeptide.

[0673] 302. The kit of any one of Aspects 210-301, wherein the binding agent is capable of selectively binding to the polypeptide.

[0674] 303. The kit of any one of Aspects 210-302, wherein the coding tag is DNA molecule, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, or a combination thereof.

[0675] 304. The kit of any one of Aspects 210-303, wherein the coding tag comprises an encoder or barcode sequence.

[0676] 305. The kit of any one of Aspects 210-304, wherein the coding tag further comprises a spacer, a binding cycle specific sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0677] 306. The kit of any one of Aspects 210-305, wherein the binding portion and the coding tag in the binding agent are joined by a linker.

[0678] 307. The kit of any one of Aspects 210-305, wherein the binding portion and the coding tag are joined by a SpyTag / SpyCatcher peptide-protein pair, a SnoopTag / SnoopCatcher peptide-protein pair, or a HaloTag / HaloTag ligand pair.

[0679] 308. The kit of any one of Aspects 210-307, wherein the reagent for transferring the information of the coding tag to the recording tag comprises a DNA ligase or an RNA ligase.

[0680] 309. The kit of any one of Aspects 210-307, wherein the reagent for transferring the information of the coding tag to the recording tag comprises a DNA polymerase, an RNA polymerase, or a reverse transcriptase.

[0681] 310. The kit of any one of Aspects 210-307, wherein the reagent for transferring the information of the coding tag to the recording tag comprises a chemical ligation reagent.

[0682] 311. The kit of Aspect 310, wherein the chemical ligation reagent is for use with single-stranded DNA.

[0683] 312. The kit of Aspect 310, wherein the chemical ligation reagent is for use with double-stranded DNA.

[0684] 313. The kit of any one of Aspects 210-312, further comprising a ligation reagent comprised of two DNA or RNA ligase variants, an adenylated variant and a constitutively non- adenylated variant.

[0685] 314. The kit of any one of Aspects 210-312, further comprising a ligation reagent comprised of a DNA or RNA ligase and a DNA / RNA deadenylase.

[0686] 315. The kit of any one of Aspects 210-314, wherein the kit additionally comprises reagents for nucleic acid sequencing methods.

[0687] 316. The kit of Aspect 315, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

[0688] 317. The kit of Aspect 315, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

[0689] 318. The kit of any one of Aspects 210-317, wherein the kit additionally comprises reagents for amplifying the extended recording tag.

[0690] 319. The kit of any one of Aspects 210-318, further comprising reagents for adding a cycle label.

[0691] 320. The kit of Aspect 319, wherein the cycle label provides information regarding the order of binding by the binding agents to the polypeptide.

[0692] 321. The kit of Aspect 319 or Aspect 320, wherein the cycle label can be added to the coding tag.

[0693] 322. The kit of Aspect 319 or Aspect 320, wherein the cycle label can be added to the recording tag.

[0694] 323. The kit of Aspect 319 or Aspect 320, wherein the cycle label can be added to the binding agent.

[0695] 324. The kit of Aspect 319 or Aspect 320, wherein the cycle label can be added independent of the coding tag, recording tab, and binding agent.

[0696] 325. The kit of any one of Aspects 210-324, wherein the order of coding tag information contained on the extended recording tag provides information regarding the order of binding by the binding agents to the polypeptide.

[0697] 326. The kit of any one of Aspects 210-325, wherein frequency of the coding tag information contained on the extended recording tag provides information regarding the frequency of binding by the binding agents to the polypeptide.

[0698] 327. The kit of any one of Aspects 210-326, which is configured for analyzing one or more polypeptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides.

[0699] 328. The kit of Aspect 327, further comprising means for partitioning the plurality of protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags optionally joined to a support(e.g., a solid support), wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments.

[0700] 329. The kit of Aspect 327 or 328, further comprising a reagent for fragmenting the plurality of protein complexes, proteins, and / or polypeptides into a plurality of polypeptides.

[0701] 330. The kit of Aspect 328, wherein the compartment is a microfluidic droplet.

[0702] 331. The kit of Aspect 328, wherein the compartment is a microwell.

[0703] 332. The kit of Aspect 328, wherein the compartment is a separated region on a surface.

[0704] 333. The kit of any one of Aspects 328-332, wherein each compartment comprises on average a single cell.

[0705] 334. A kit of any one of Aspects 327-333, further comprising a reagent for labeling the plurality of protein complexes, proteins, or polypeptides with a plurality of universal DNA tags.

[0706] 335. The kit of any one of Aspects 328-334, wherein the reagent for transferring the compartment tag information to the recording tag associated with a polypeptide comprises a primer extension or ligation reagent.

[0707] 336. The kit of any one of Aspects 328-335, wherein the support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0708] 337. The kit of any one of Aspects 328-335, wherein the support comprises a bead.

[0709] 338. The kit of Aspect 337, wherein the bead is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

[0710] 339. The kit of any one of Aspects 328-338, wherein the compartment tag comprises a single stranded or double stranded nucleic acid molecule.

[0711] 340. The kit of any one of Aspects 328-339, wherein the compartment tag comprises a barcode and optionally a UMI.I l l

[0712] 341. The kit of Aspect 340, wherein the support is a bead and the compartment tag comprises a barcode, further wherein beads comprising the plurality of compartment tags joined thereto are formed by split-and-pool synthesis.

[0713] 342. The kit of Aspect 340, wherein the support is a bead and the compartment tag comprises a barcode, further wherein beads comprising a plurality of compartment tags joined thereto are formed by individual synthesis or immobilization.

[0714] 343. The kit of any one of Aspects 328-342, wherein the compartment tag is a component within a recording tag, wherein the recording tag optionally further comprises a spacer, a barcode sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

[0715] 344. The kit of any one of Aspects 328-343, wherein the compartment tags further comprise a functional moiety capable of reacting with an internal amino acid, the peptide backbone, or N-terminal amino acid on the plurality of protein complexes, proteins, or polypeptides.

[0716] 345. The kit of Aspect 344, wherein the functional moiety is an aldehyde, an azide / alkyne, or a malemide / thiol, or an epoxide / nucleophile, or an inverse electron demain Diels- Alder (iEDDA) group.

[0717] 346. The kit of Aspect 344, wherein the functional moiety is an aldehyde group.

[0718] 347. The kit of any one of Aspects 328-346, wherein the plurality of compartment tags is formed by: printing, spotting, ink-jetting the compartment tags into the compartment, or a combination thereof.

[0719] 348. The kit of any one of Aspects 328-347, wherein the compartment tag further comprises a polypeptide.

[0720] 349. The kit of Aspect 348, wherein the compartment tag polypeptide comprises a protein ligase recognition sequence.

[0721] 350. The kit of Aspect 349, wherein the protein ligase is butelase I or a homolog thereof.

[0722] 351. The kit of any one of Aspects 328-350, wherein the reagent for fragmenting the plurality of polypeptides comprises a protease.

[0723] 352. The kit of Aspect 351, wherein the protease is a metalloprotease.

[0724] 353. The kit of Aspect 352, further comprising a reagent for modulating the activity of the metalloprotease, e.g., a reagent for photo-activated release of metallic cations of the metalloprotease.

[0725] 354. The kit of any one of Aspects 328-353, further comprising a reagent for subtracting one or more abundant proteins from the sample prior to partitioning the plurality of polypeptides into the plurality of compartments.

[0726] 355. The kit of any one of Aspect 328-354, further comprising a reagent for releasing the compartment tags from the support prior to joining of the plurality of polypeptides with the compartment tags.

[0727] 356. The kit of Aspect 328, further comprising a reagent for joining the compartment tagged polypeptides to a support in association with recording tags.

[0728] 357. A method for screening for a polypeptide functionalizing reagent, an amino acid eliminating reagent and / or a reaction condition, which method comprises the steps of:(a) contacting a polynucleotide with a polypeptide functionalizing reagent and / or an amino acid eliminating reagent under a reaction condition; and(b) assessing the effect of step (a) on said polynucleotide, optionally to identify a polypeptide functionalizing reagent, an amino acid eliminating reagent and / or a reaction condition that has no or minimal effect on said polynucleotide.

[0729] 358. The method of Aspect 357, wherein the polynucleotide comprises at least about 4 nucleotides.

[0730] 359. The method of Aspect 357, wherein the polynucleotide comprises at most about 10 kb nucleotides.

[0731] 360. The method of any one of Aspects 357-359, wherein the polynucleotide is a DNA polynucleotide.

[0732] 361. The method of any one of Aspects 357-360, wherein the polynucleotide is genomic DNA or the method is conducted in the presence of genomic DNA.

[0733] 362. The method of any one of Aspects 357-360, wherein the polynucleotide is an isolated polynucleotide.

[0734] 363. The method of any one of Aspects 357-360, wherein the polynucleotide is a part of a binding agent for the polypeptide.

[0735] 364. The method of any one of Aspects 357-363, wherein the polynucleotide is contacted with the polypeptide functionalizing reagent and / or the amino acid eliminating reagent under a reaction condition in the absence of the polypeptide.

[0736] 365. The method of any one of Aspects 357-363, wherein the polynucleotide is contacted with the polypeptide functionalizing reagent and / or the amino acid eliminating reagent under a reaction condition in the presence of the polypeptide.

[0737] 366. The method of Aspect 365, wherein the polynucleotide is a part of a binding agent for the polypeptide.

[0738] 367. The method of any one of Aspects 357-366, wherein the polypeptide functionalizing reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):RLNH (I)or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; and optionally wherein when R3isR1ancj R2are not both H;(ii) a compound of Formula (II):(Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (III)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, NR13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH

[0739] 368. The method of any one of Aspects 357-367, wherein the amino acid eliminating reagent is a chemical cleavage reagent or an enzymatic cleavage reagent.

[0740] 369. The method of Aspect 368, wherein the amino acid eliminating reagent is a carboxypeptidase or aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; a mild Edman degradation reagent; an Edmanase enzyme; TFA; a base; or any combination thereof.

[0741] 370. The method of any one of Aspects 357-369, wherein the reaction condition comprises reaction time, reaction temperature, reaction pH, solvent type, co-solvent, catalysts, and ionic liquids, and electrochemical potential.

[0742] 371. The method of any one of Aspects 357-370, wherein step (a) is conducted in a solution.

[0743] 372. The method of any one of Aspects 357-370, wherein step (a) is conducted on a solid phase.

[0744] 373. The method of any one of Aspects 357-372, wherein the effect of step (a) on the polynucleotide is assessed by assessing the presence, absence or quantity of modification of the polynucleotide by the polypeptide functionalizing reagent, the amino acid eliminating reagent and / or the reaction condition.

[0745] 374. The method of any one of Aspects 357-373, wherein less than 50% modification of the polynucleotide, as compared to a corresponding polynucleotide not contacted with a polypeptide functionalizing reagent and / or an amino acid eliminating reagent under a reaction condition, identifies the polypeptide functionalizing reagent, the amino acid eliminating reagent and / or the reaction condition that has no or minimal effect on the polynucleotide.

[0746] 375. A kit for screening for a polypeptide functionalizing reagent, an amino acid eliminating reagent and / or a reaction condition, comprising: (a) a polynucleotide; (b) a polypeptide functionalizing reagent and / or an amino acid eliminating reagent; (c) means for assessing the effect of said polypeptide functionalizing reagent, said amino acid eliminating reagent and / or a reaction condition for polypeptide functionalization or elimination on said polynucleotide.

[0747] 376. The kit of Aspect 375, wherein the polypeptide functionalizing reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; andoptionally wherein when R isR1and R2are not both H;(ii) a compound of Formula (II):or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (III)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -S(0)2Rj, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formul IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, NR13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR is H or OH.

[0748] 377. The kit of Aspect 375 or Aspect 376, which comprises a polypeptide functionalizing reagent and an amino acid eliminating reagent.

[0749] 378. A method of sequencing a polypeptide comprising:(a) affixing the polypeptide to a support or substrate, or providing the polypeptide in a solution;(b) functionalizing the N-terminal amino acid (NTAA) of the polypeptide with a chemical reagent, wherein the chemical reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, -NRdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; andoptionally wherein when R isand R2are not both H;(ii) a compound of Formula (II):H (Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5N=C=S (Hi)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula (IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG is N, NR , or CR13R14;G2iis N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH;(c) contacting the polypeptide with a plurality of binding agents each comprising a binding portion capable of binding to the functionalized NTAA and a detectable label;(d) detecting the detectable label of the binding agent bound to the polypeptide, thereby identifying the N-terminal amino acid of the polypeptide;(e) eliminating the functionalized NTAA to expose a new NTAA; and(f) repeating steps (b) to (d) to determine the sequence of at least a portion of the polypeptide.

[0750] 379. The method of Aspect 378, wherein step (b) is conducted before step (c).

[0751] 380. The method of Aspect 378, wherein step (b) is conducted after step (c) and before step (d).

[0752] 381. The method of Aspect 378, wherein step (b) is conducted after both step (c) and step (d).

[0753] 382. The method of any one of Aspects 378-381, wherein the polypeptide is obtained by fragmenting a protein from a biological sample.

[0754] 383. The method of any one of Aspects 378-382, wherein the support or substrate is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0755] 384. The method of any one of Aspects 378-383, wherein the NTAA is eliminated by chemical cleavage or enzymatic cleavage from the polypeptide.

[0756] 385. The method of any one of Aspects 378-384, wherein the NTAA is eliminated by a carboxypeptidase or aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; mild Edman degradation; Edmanase enzyme; TFA, a base; or any combination thereof.

[0757] 386. The method of any one of Aspects 378-385, wherein the polypeptide is covalently affixed to the support or substrate.

[0758] 387. The method of any one of Aspects 378-386, wherein the support or substrate is optically transparent.

[0759] 388. The method of any one of Aspects 378-387, wherein the support or substrate comprises a plurality of spatially resolved attachment points and step a) comprises affixing the polypeptide to a spatially resolved attachment point.

[0760] 389. The method of Aspect any one of Aspects 378-388, wherein the binding portion of the binding agent comprises a peptide or protein.

[0761] 390. The method of any one of Aspects 378-389, wherein the binding portion of the binding agent comprises an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS (such as ClpS2) or variant, mutant, or modified protein thereof; a UBR box protein or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or an antibody or binding fragment thereof; or any combination thereof.

[0762] 391. The method of any one of Aspects 378-390, wherein the chemical reagent comprises a conjugate selected from the group consisting ofFormula (I)-Q,wherein R1, R2, and R3are as defined for Formula (I) in Aspect 1, and Q is a ligand;Formula (II)-Q,wherein R4is as defined for For 1, and Q is a ligand;Formula (III)-Q,wherein R5is as defined for Formula (III) in Aspect 1, and Q is a ligand;R6Formula (IV)-Q,wherein R6and R7are as defined for Formula (IV) in Aspect 1, and Q is a ligwherein R8and R9are as defined for Formula (V) in Aspect 1, and Q is a ligand;(MLn)-Q Formula (VI)-Q,wherein M, L, and n are as defined for Formula (VI) in Aspect 1, and Q is a ligand;Formula (VII)-Q,wherein R10, R11, R12, R15, G1, G2, and p are as defined for Formula (VII) in Aspect 1, and Q is a ligand.

[0763] 392. The method of any one of Aspects 378-391, wherein step (b) comprises functionalizing the NTAA with a second chemical reagent selected from Formula (Villa) and (Vlllb):OR13(Villa) or a salt or conjugate thereof,whereinR13is H, Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, wherein the Ci-6alkyl, aryl, heteroaryl, cycloalkyl, and heterocycloalkyl are each unsubstituted or substituted; andR13— X (VHIb)whereinR13is Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, each of which is unsubstituted or substituted; andX is a halogen.

[0764] 393. The method of any one of Aspects 378-392, wherein the polypeptide is a partially or completely digested protein.

[0765] 394. A method of sequencing a plurality of polypeptide molecules in a sample comprising:(a) affixing the polypeptide molecules in the sample to a plurality of spatially resolved attachment points on a support or substrate;(b) functionalizing the N-terminal amino acid (NTAA) of the polypeptide molecules with a chemical reagent, wherein the chemical reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;RA, RB, and RCare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORE, or -SRF, wherein the heteroaryl is unsubstituted or substituted;RD, RE, and RFare each independently H or Ci-6alkyl; andoptionally wherein when R3is N¾^RIancj R2ARE ΗΟ^ JJ.(ii) a compound of Formula (II):H (II)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORG; andRGis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5N=C=S (Hi)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;RH, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, R13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH;(c) contacting the polypeptides with a plurality of binding agents each comprising a binding portion capable of binding to the functionalized NTAA and a detectable label;(d) for a plurality of polypeptides molecule that are spatially resolved and affixed to the support or substrate, optically detecting the fluorescent label of the probe bound to eachpolypeptide;(e) eliminating the functionalized NTAA of each of the polypeptides; and(f) repeating steps b) to d) to determine the sequence of at least a portion of one or more of the plurality of polypeptide molecules that are spatially resolved and affixed to the support or substrate.

[0766] 395. The method of Aspect 394, wherein step (b) is conducted before step (c).

[0767] 396. The method of Aspect 394, wherein step (b) is conducted after step (c) and before step (d).

[0768] 397. The method of Aspect 394, wherein step (b) is conducted after both step (c) and step (d).

[0769] 398. The method of any one of Aspects 394-397, wherein the sample comprises a biological fluid, cell extract or tissue extract.

[0770] 399. The method of any one of Aspects 394-398, further comprising comparing the sequence of at least one polypeptide molecule determined in step e) to a reference protein sequence database.

[0771] 400. The method of any one of Aspects 394-399, further comprising comparing the sequences of each polypeptide determined in step e), grouping similar polypeptide sequences and counting the number of instances of each similar polypeptide sequence.

[0772] 401. The method of any one of Aspects 394-400, wherein the fluorescent label is a fluorescent moiety, color-coded nanoparticle or quantum dot.

[0773] 402. A kit for sequencing a polypeptide comprising:(a) a reagent for affixing the polypeptide to a support or substrate, or a reagent for providing the polypeptide in a solution;(b) a reagent for functionalizing the N-terminal amino acid (NTAA) of the polypeptide, wherein the reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):R' N^R3H (I)or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, - RdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; andoptionally wherein when R3is N¾¾^ ancj R2ARE nQ^ JJ.(ii) a compound of Formula (II):H(Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)Rg, or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Cialkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5-N=C=S (Hi)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -0Rk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG1is N, R13, or CR13R14;G2is N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH; and(c) a binding agent comprising a binding portion capable of binding to thefunctionalized NTAA and a detectable label.

[0774] 403. The kit of Aspect 402, wherein the kit additionally comprises a reagent for eliminating the functionalized NTAA to expose a new NTAA.

[0775] 404. The kit of Aspect 402 or Aspect 403, wherein the polypeptide is obtained by fragmenting a protein from a biological sample.

[0776] 405. The kit of any one of Aspects 402-404, wherein the support or substrate is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

[0777] 406. The kit of any one of Aspects 403-405, wherein the reagent for eliminating the functionalized NTAA is a carboxypeptidase or aminopeptidase or variant, mutant, or modified protein thereof; a hydrolase or variant, mutant, or modified protein thereof; mild Edman degradation; Edmanase enzyme; TFA, a base; or any combination thereof.

[0778] 407. The kit of any one of Aspects 402-406, wherein the polypeptide is covalently affixed to the support or substrate.

[0779] 408. The kit of any one of Aspects 402-407, wherein the support or substrate is optically transparent.

[0780] 409. The kit of any one of Aspects 402-408, wherein the support or substrate comprises a plurality of spatially resolved attachment points and step a) comprises affixing polypeptide to a spatially resolved attachment point.

[0781] 410. The kit of Aspect any one of Aspects 402-409, wherein the binding portion of the binding agent comprises a peptide or protein.

[0782] 411. The kit of any one of Aspects 402-410, wherein the binding portion of the binding agent comprises an aminopeptidase or variant, mutant, or modified protein thereof; an aminoacyl tRNA synthetase or variant, mutant, or modified protein thereof; an anticalin or variant, mutant, or modified protein thereof; a ClpS (such as ClpS2) or variant, mutant, or modified protein thereof; a UBR box protein or variant, mutant, or modified protein thereof; or a modified small molecule that binds amino acid(s), i.e. vancomycin or a variant, mutant, or modified molecule thereof; or an antibody or binding fragment thereof; or any combination thereof.

[0783] 412. The kit of any one of Aspects 402-411, wherein the chemical reagent comprises a conjugate selected from the group consisting ofFormula (I)-Q,wherein R1, R2, and R3are as defined for Formula (I) in Aspect 1, and Q is a ligand;Formula (II)-Q,wherein R4defined for Formula (II) in Aspect 1, and Q is a ligand;(III)-Q,wherein R5defined for Formula (III) in Aspect 1, and Q is a ligand;wherein R6and R7are as defined for Formul in Aspect 1, and Q is a ligand;Formula (V)-Q,wherein R8and R9are as defined for Formula (V) in Aspect 1, and Q is a ligand;(MLn)-Q Formula (VI)-Q,wherein M, L, and n are as defined for Formula (VI) in Aspect 1, and Q is a ligand;wherein R10, R11, R12, R15, G1, G2, and p are as defined for Formula (VII) in Aspect 1, and Q is a ligand.

[0784] Aspect 413. The kit of any one of Aspects 402-412, the kit includes a second chemical reagent selected from Formula (Villa) and (Vlllb):0^ 13R3(Villa) or a salt or conjugate thereof,whereinR13is H, Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, wherein the Ci-6alkyl, aryl, heteroaryl, cycloalkyl, and heterocycloalkyl are each unsubstituted or substituted; andR13-X (Vlllb)whereinR is Ci-6alkyl, aryl, heteroaryl, cycloalkyl, or heterocycloalkyl, each of which is unsubstituted or substituted; andX is a halogen.

[0785] 414. The method of any one of Aspects 402-413, wherein the polypeptide is a partially or completely digested protein.

[0786] 415. A kit for sequencing a plurality of polypeptide molecules in a sample comprising:(a) a reagent for affixing the polypeptide molecules in the sample to a plurality of spatially resolved attachment points on a support or substrate;(b) a reagent for functionalizing the N-terminal amino acid (NTAA) of the polypeptide molecules, wherein the reagent comprises a compound selected from the group consisting of(i) a compound of Formula (I):or a salt or conjugate thereof,whereinR1and R2are each independently H, Ci-ealkyl, cycloalkyl, -C(0)Ra, -C(0)ORb, or -S(0)2Rc;Ra, Rb, and Rcare each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;R3is heteroaryl, -NRdC(0)ORe, or -SRf, wherein the heteroaryl is unsubstituted or substituted;Rd, Re, and Rfare each independently H or Ci-6alkyl; andoptionally wherein when R isand R2are not both H;(ii) a compound of Formula (II):H (Π)or a salt or conjugate thereof,whereinR4is H, Ci-ealkyl, cycloalkyl, -C(0)R , or -C(0)ORg; andRgis H, Ci-6alkyl, C2-6alkenyl, Ci-6haloalkyl, or arylalkyl, wherein the Ci6alkenyl, Ci-6haloalkyl, and arylalkyl are each unsubstituted or substituted;(iii) a compound of Formula (III):R5N=C=S (Hi)or a salt or conjugate thereof,whereinR5is Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl;wherein the Ci-6alkyl, C2-6alkenyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl are each unsubstituted or substituted with one or more groups selected from the group consisting of halo, - R^t1, -8(0)^, or heterocyclyl;Rh, R1, and R> are each independently H, Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, or heteroaryl, wherein the Ci-6alkyl, Ci-6haloalkyl, arylalkyl, aryl, and heteroaryl are each unsubstituted or substituted;(iv) a compound of Formula (IV):or a salt or conjugate thereof,whereinR6and R7are each independently H, Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, or cycloalkyl, wherein the Ci-6alkyl, -C02Ci-4alkyl, -ORk, aryl, and cycloalkyl are each unsubstituted or substituted; andRkis H, Ci-6alkyl, or heterocyclyl, wherein the Ci-6alkyl and heterocyclyl are each unsubstituted or substituted;(v) a compound of Formula (V):or a salt or conjugate thereof,whereinR8is halo or -ORm;Rmis H, Ci-6alkyl, or heterocyclyl; andR9is hydrogen, halo, or Ci-6haloalkyl;(vi) a metal complex of Formula (VI):MLn (VI)or a salt or conjugate thereof,whereinM is a metal selected from the group consisting of Co, Cu, Pd, Pt, Zn, and Ni;L is a ligand selected from the group consisting of -OH, -OH2, 2,2'-bipyridine (bpy), l,5dithiacyclooctane (dtco), l,2-bis(diphenylphosphino)ethane (dppe), ethylenediamine (en), and triethylenetetramine (trien); andn is an integer from 1-8, inclusive;wherein each L can be the same or different; and(vii) a compound of Formula (VII):or a salt or conjugate thereof,whereinG is N, NR , or CR13R14;G2iis N or CH;p is 0 or 1;R10, R11, R12, R13, and R14are each independently selected from the group consisting of H, Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine , wherein the Ci-6alkyl, Ci-6haloalkyl, Ci-6alkylamine, and Ci-6alkylhydroxylamine are each unsubstituted or substituted, and R10and R11can optionally come together to form a ring; andR15is H or OH; and(c) a binding agent comprising a binding portion capable of binding to thefunctionalized NTAA and a detectable label.

[0787] 416. The kit of Aspect 415, wherein the kit additionally comprises a reagent for eliminating the functionalized NTAA to expose a new NTAA.

[0788] Aspect 417. The kit of Aspect 415 or 416, wherein the sample comprises a biological fluid, cell extract or tissue extract.

[0789] Aspect 418. The kit of any one of Aspects 415-417, wherein the fluorescent label is a fluorescent moiety, color-coded nanoparticle or quantum dot.

[0790] In any of the preceding embodiments, the recording tag and / or the coding tag can be a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0791] In any of the preceding embodiments, the recording tag and / or the coding tag can be a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0792] In any of the preceding embodiments, the recording tag and / or the coding tag can comprise a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0793] In any of the preceding embodiments, the coding tag can be a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer, while the recording tag is a sequenceable polymer. In some embodiments, the coding tag (a small molecule, subunit, or monomer etc.) can be added to the recording tag in order to form a sequenceable polymer, akin to beads {e.g., various coding tags) on a string {e.g., the extended recording tag).

[0794] In any of the preceding embodiments, the extended recording tag and / or the extended coding tag can be a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0795] In one aspect, disclosed herein is a method, comprising: (a) contacting an analyte with a first binding agent capable of binding to the analyte, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the analyte is associated with a recording portion joined to a support, and the analyte and / or the recording portion is immobilized to a support; (b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion; (c) contacting the analyte with a second binding agent capable of binding to the analyte, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent; (d) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and (e) analyzing the second order extended recording portion. In one embodiment, the method further comprises between steps (d) and (e), the following steps: (x) repeating steps (c) and (d) one or more times by replacing the second binding agent with a third (or higher order) binding agent capable of binding to the analyte, wherein the third (or higher order) binding agent comprises a third (or higher order) coding portion with identifying information regarding the third (or higher order) bind agent; and (y) transferring the information of the third (or higher order) coding portion to the second (or higher order) extended recording portion to generate a third (or higher order) extended recording portion, wherein the third (or higher order) extended recording portion is analyzed in step (e).

[0796] In any of the preceding embodiments, the recording portion can be a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0797] In any of the preceding embodiments, the recording portion can be a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer. In someembodiments, the first, second, third, and / or higher order coding portion comprises a small molecule, and / or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0798] In any of the preceding embodiments, the first, second, third, and / or higher order coding portion can be a small molecule, or a subunit, monomer, residue, or building block of asequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0799] In any of the preceding embodiments, the first order extended recording portion, second order extended recording portion, third order extended recording portion, and / or higher order extended recording portion can be a sequenceable polymer, such as a polynucleotide or a non- nucleic acid sequenceable polymer.

[0800] In another aspect, disclosed herein is a method, comprising: (a) contacting a polypeptide with a first binding agent capable of binding to one or more N-terminal, internal, or C-terminal amino acid of the polypeptide, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the polypeptide is associated with a recording portion joined to a support, and the polypeptide and / or the recording portion is immobilized to a support; (b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion; (c) contacting the analyte with a second binding agent capable of binding to a different one or more N-terminal, internal, or C-terminal amino acid of the polypeptide, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent; (d) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and (e) analyzing the second order extended recording portion. In one embodiment, the one or more N-terminal, internal, or C-terminal amino acid and / or the different one or more N-terminal, internal, or C-terminal amino acid of the polypeptide is a modified amino acid, such as a modified N-terminal amino acid (NTAA).

[0801] In another aspect, disclosed herein is a method, comprising: (a) contacting a polypeptide with a first binding agent capable of binding to one or more N-terminal or C-terminal amino acid of the polypeptide, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the polypeptide is associated with a recording portion joined to a support, and the polypeptide and / or the recording portion is immobilized to a support; (b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion; (c) eliminating the one or more N-terminal or C-terminal aminoacid of the polypeptide, to expose a different one or more N-terminal or C-terminal amino acid of the polypeptide; (d) contacting the analyte with a second binding agent capable of binding to the different one or more N-terminal or C-terminal amino acid of the polypeptide, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent; (e) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and (f) analyzing the second order extended recording portion. In one embodiment, the one or more N-terminal or C- terminal amino acid and / or the different one or more N-terminal or C-terminal amino acid of the polypeptide is a modified amino acid, such as a modified N-terminal amino acid (NTAA).

[0802] In any of the preceding embodiments, the recording portion of step (a) can be a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0803] In any of the preceding embodiments, the recording portion of step (a) can be a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer. In some embodiments, the first or second order coding portion comprises a small molecule, and / or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0804] In any of the preceding embodiments, the first or second order coding portion can be a small molecule, or a subunit, monomer, residue, or building block of a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0805] In any of the preceding embodiments, the first order extended recording portion or second order extended recording portion can be a sequenceable polymer, such as a polynucleotide or a non-nucleic acid sequenceable polymer.

[0806] In any of the preceding embodiments, the sequenceable polymer can comprise one or more blockade group. In one embodiment, the one or more blockade group is capable of generating a signature current blockade signal when the sequenceable polymer passes through a nanopore.

[0807] In any of the preceding embodiments, the sequenceable polymer can comprise one or more binding moiety capable of binding to a binding agent that stalls the sequenceable polymer when passing through a nanopore.

[0808] In any of the preceding embodiments, the sequenceable polymer can comprise one or more structure capable of stalling the sequenceable polymer when passing through a nanopore. In one embodiment, the one or more structure comprises a secondary structure, such as an intrinsic meta-stable secondary structure.

[0809] In any of the preceding embodiments, the sequenceable polymer can comprise a polymer built using phosphoramidite chemistry, or a peptoid polymer, or a combination thereof.

[0810] In another aspect, disclosed herein is a kit, comprising any molecule, molecular complex or conjugate, reagent (e.g., chemical or biological), agent, structure (e.g., support, surface, particle, or bead), reaction intermediate, reaction product, binding complex, or any other article of manufacture disclosed and / or used in the method of any of the preceding embodiments, or any combination thereof.

[0811] Any of the above-mentioned kit components, and any molecule, molecular complex or conjugate, reagent (e.g., chemical or biological reagents), agent, structure (e.g., support, surface, particle, or bead), reaction intermediate, reaction product, binding complex, or any other article of manufacture disclosed and / or used in the exemplary kits and methods, may be provided separately or in any suitable combination in order to form a kit. The kit may optionally comprise instruction for use, for example, in highly-parallel, high throughput digital analysis (such as macromolecule analysis), particularly polypeptide analysis.Brief Description of the Drawings

[0812] Non-limiting embodiments of the present disclosure will be described by way of example with reference to the accompanying figures, which are schematic and are not intended to be drawn to scale. For purposes of illustration, not every component is labeled in every figure, nor is every component of each embodiment of the invention shown where illustration is not necessary to allow those of ordinary skill in the art to understand the present disclosure.

[0813] Figures 1A-B: Figure 1A illustrates key for functional elements shown in the figures.Thus in one embodiment, provided herein is a recording tag or an extended recording tag, comprising one or more universal primer sequences (or one or more pairs of universal primer sequences, for example, one universal prime of the pair at the 5' end and the other of the pair at the3' end of the recording tag or extended recording tag), one or more barcode sequences that can identify the recording tag or extended recording tag among a plurality of recording tags or extended recording tags, one or more UMI sequences, one or more spacer sequences, and / or one or more encoder sequences (also referred to as the coding sequence, e.g., of a coding tag). In certain embodiments, the extended recording tag comprises (i) one universal primer sequence, one barcode sequence, one UMI sequence, and one spacer (all from the unextended recording tag), (ii) one or more "cassettes" arranged in tandem, each cassette comprising an encoder sequence for a binding agent, a UMI sequence, and a spacer, and each cassette comprises sequence information from a coding tag, and (iii) another universal primer sequence, which may be provided by the coding tag of the coding agent in the rP1binding cycle, where n is an integer representing the number of binding cycle after which assay read out is desired. In one embodiment, after a universal primer sequence is introduced into an extended recoding tag, the binding cycles may continue, the extended recording tag may be further extended, and one or more additional universal primer sequences may be introduced. In that case, amplification and / or sequencing of the extended recording tag may be done using any combination of the universal primer sequences. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof {e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0814] Figure IB illustrates a general overview of transducing or converting a protein code to a nucleic acid {e.g., DNA) code where a plurality of proteins or polypeptides are fragmented into a plurality of peptides, which are then converted into a library of extended recording tags, representing the plurality of peptides. The extended recording tags constitute a DNA Encoded Library (DEL) representing the peptide sequences. The library can be appropriately modified to sequence on any Next Generation Sequencing (NGS) platform. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof {e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0815] Figures 2A-2D illustrate an example of polypeptide (e.g., protein) analysis according to the methods disclosed herein, using multiple cycles of binding agents (e.g., antibodies, anticalins, N-recognins proteins (e.g., ClpSs, or UBR box proteins, etc.), and variants / homologues thereof, and aptamers etc.) comprising coding tags interacting with an immobilized protein that is co-localized or co-labeled with a single or multiple recording tags. In this example, the recording tag comprises a universal priming site, a barcode (e.g., partition barcode, compartment barcode, and / or fraction barcode), an optional unique molecular identifier (UMI) sequence, and optionally a spacer sequence (Sp) used in information transfer between the coding tag and the recording tag (or an extended recording tag). The spacer sequence (Sp) can be constant across all binding cycles, be binding agent specific, and / or be binding cycle number specific (e.g., used for "clocking" the binding cycles). In this example, the coding tag comprises an encoder sequence providing identifying information for the binding agent (or a class of binding agents, for example, a class of binders that all specifically bind to a terminal amino acid, such as a modified N-terminal Q as shown in Figure 3), an optional UMI, and a spacer sequence that hybridizes to the complementary spacer sequence on the recording tag, facilitating transfer of coding tag information to the recording tag (e.g., by primer extension, also referred to herein as polymerase extension). Ligation may also be used to transfer sequence information and in that case, a spacer sequence may be used but is not necessary. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle- specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non- nucleic acid sequenceable polymer.

[0816] Figure 2A illustrates a process of creating an extended recording tag through the cyclic binding of cognate binding agents to a analyte (such as a protein or protein complex), and corresponding information transfer from the binding agent's coding tag to the analyte' s recording tag. After a series of sequential binding and coding tag information transfer steps, the final extended recording tag is produced, containing binding agent coding tag information including encoder sequences from "«" binding cycles providing identifying information for the binding agents (e.g., antibody 1 (Abl), antibody 2 (Ab2), antibody 3 (Ab3), ... antibody "w" (Abw)), abarcode / optional UMI sequence from the recording tag, an optional UMI sequence from the binding agent's coding tag, and flanking universal priming sequences at each end of the library construct to facilitate amplification and / or analysis by digital next-generation sequencing. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0817] Figure 2B illustrates an example of a scheme for labeling a protein with DNA barcoded recording tags. In the top panel, N-hydroxysuccinimide (NHS) is an amine reactive coupling agent, and Dibenzocyclooctyl (DBCO) is a strained alkyne useful in "click" coupling to the surface of a solid substrate. In this scheme, the recording tags are coupled to ε amines of lysine (K) residues (and optionally N-terminal amino acids) of the protein via NHS moieties. In the bottom panel, a heterobifunctional linker, NHS-alkyne, is used to label the ε amines of lysine (K) residues to create an alkyne "click" moiety. Azide-labeled DNA recording tags can then easily be attached to these reactive alkyne groups via standard click chemistry. Moreover, the DNA recording tag can also be designed with an orthogonal methyltetrazine (mTet) moiety for downstream coupling to a trans- cyclooctene (TCO)-derivatized sequencing substrate via an inverse Electron Demand Diels- Alder (iEDDA) reaction. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof {e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0818] Figure 2C illustrates two examples of the protein analysis methods using recording tags. In the top panel, analytes such as protein macromolecules are immobilized on a solid support via a capture agent and optionally cross-linked. Either the protein or capture agent may co-localize or be labeled with a recording tag. In the bottom panel, proteins with associated recording tags are directly immobilized on a solid support. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, ifapplicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0819] Figure 2D illustrates an example of an overall workflow for a simple proteinimmunoassay using DNA encoding of cognate binders and sequencing of the resultant extended recording tag. The proteins can be sample barcoded (i.e., indexed) via recording tags and pooled prior to cyclic binding analysis, greatly increasing sample throughput and economizing on binding reagents. This approach is effectively a digital, simpler, and more scalable approach to performing reverse phase protein assays (RPPA), allowing measurement of protein levels (such as expression levels) in a large number of biological samples simultaneously in a quantitative manner. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0820] Figures 3A-D illustrate a process for a degradation-based polypeptide sequencing assay by construction of an extended recording tag (e.g., DNA sequence) representing the polypeptide sequence. This is accomplished through an Edman degradation-like approach using a cyclic process, such as N-terminal amino acid (NTAA) binding, coding tag information transfer to a recording tag attached to the polypeptide, terminal amino acid(s) cleavage (such as NTAA cleavage), and repeating the process in a cyclic manner, for example, all on a solid support.Provided is an overview of an exemplary construction of an extended recording tag from N-terminal degradation of a peptide: (A) N-terminal amino acid of a peptide is labeled (e.g., with aphenylthiocarbamoyl (PTC), dinitrophenyl (DNP), sulfonyl nitrophenyl (SNP), acetyl, or guanidindyl moiety); (B) shows a binding agent and an associated coding tag bound to the labeled NTAA; (C) shows the polypeptide bound to a solid support (e.g., bead) and associated with a recording tag (e.g., via a trifunctional linker), wherein upon binding of the binding agent to the NTAA of the polypeptide, information of the coding tag is transferred to the recording tag (e.g., via primer extension or ligation, including single strand ligation or double strand ligation or blunt endligation or sticky end ligation) to generate an extended recording tag; (D) the labeled NTAA is cleaved via chemical or biological (e.g., enzymatic) means to expose a new NTAA. As illustrated by the arrows, the cycle is repeated "«" times to generate a final extended recording tag. The final extended recording tag is optionally flanked by universal priming sites to facilitate downstream amplification and / or DNA sequencing. The forward universal priming site (e.g., Illumina's P5-S1 sequence) can be part of the original recording tag design and the reverse universal priming site (e.g., Illumina's P7-S2' sequence) can be added as a final step in the extension of the recording tag. This final step may be done independently of a binding agent. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0821] Figures 4A-B illustrate exemplary protein sequencing workflows according to the methods disclosed herein. Figure 4A illustrates exemplary work flows with alternative modes outlined in light grey dashed lines, with a particular embodiment shown in boxes linked by arrows. Alternative modes for each step of the workflow are shown in boxes below the arrows. Figure 4B illustrates options in conducting a cyclic binding and coding tag information transfer step to improve the efficiency of information transfer. Multiple recording tags per molecule can be employed. Moreover, for a given binding event, the transfer of coding tag information to the recording tag can be conducted multiples times, or alternatively, a surface amplification step can be employed to create copies of the extended recording tag library, etc. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0822] Figures 5A-B illustrate an overview of an exemplary construction of an extended recording tag using primer extension to transfer identifying information of a coding tag of a binding agent to a recording tag associated with an analyte such as a macromolecule (e.g., a polypeptide) to generate an extended recording tag. A coding tag comprising a unique encoder sequence withidentifying information regarding the binding agent is optionally flanked on each end by a common spacer sequence (Sp'). Figure 5A illustrates an NTAA binding agent comprising a coding tag binding to an NTAA of a polypeptide which is labeled with a recording tag and linked to a bead. The recording tag anneals to the coding tag via complementary spacer sequences (Sp anneals to Sp'), and a primer extension reaction mediates transfer of coding tag information to the recording tag using the spacer (Sp) as a priming site. The coding tag is illustrated as a duplex with a single stranded spacer (Sp') sequence at the terminus distal to the binding agent. This configuration minimizes hybridization of the coding tag to internal sites in the recording tag and favors hybridization of the recording tag's terminal spacer (Sp) sequence with the single stranded spacer overhang (Sp') of the coding tag. Moreover, the extended recording tag may be pre-annealed with one or more oligonucleotides (e.g., complementary to an encoder and / or a spacer sequence) to block hybridization of the coding tag to internal recording tag sequence elements. Figure 5B shows a final extended recording tag produced after "«" cycles of binding ("***" represents intervening binding cycles not shown in the extended recording tag) and transfer of coding tag information and the addition of a universal priming site at the 3' end. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0823] Figure 6 illustrates coding tag information being transferred to an extended recording tag via enzymatic ligation. Two different analytes are shown with their respective recording tags, with recording tag extension proceeding in parallel. Ligation can be facilitated by designing the double stranded coding tags so that the spacer sequences (Sp') have a "sticky end" overhang on one strand that anneals with a complementary spacer (Sp) on the recording tag. This "sticky end" (also known as "cohesive end") can be 0-8 bases in length, for example, around 2-4 bases. The complementary strand of the double stranded coding tag, after being ligated to the recording tag, transfers information to the recording tag. The complementary strand may comprise another spacer sequence, which may be the same as or different from the Sp of the recording tag before the ligation. When ligation is used to extend the recording tag, the direction of extension can be 5' to 3'as illustrated, or optionally 3' to 5' . In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0824] Figure 7 illustrates a "spacer-less" approach of transferring coding tag information to a recording tag via chemical ligation to link the 3' nucleotide of a recording tag or extended recording tag to the 5' nucleotide of the coding tag (or its complement) without inserting a spacer sequence into the extended recording tag. The orientation of the extended recording tag and coding tag could also be inverted such that the 5' end of the recording tag is ligated to the 3' end of the coding tag (or complement). In the example shown, hybridization between complementary "helper"oligonucleotide sequences on the recording tag ("recording helper") and the coding tag are used to stabilize the complex to enable specific chemical ligation of the recording tag to coding tag complementary strand. The resulting extended recording tag is devoid of spacer sequences. Also illustrated is a "click chemistry" version of chemical ligation (e.g., using azide and alkyne moieties (shown as a triple line symbol)) which can employ DNA, PNA, or similar nucleic acid polymers. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di- tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0825] Figures 8A-B illustrate an exemplary method of writing of post-translationalmodification (PTM) information of a polypeptide into an extended recording tag prior to N-terminal amino acid degradation. Figure 8A: A binding agent comprising a coding tag with identifying information regarding the binding agent (e.g., a phosphotyrosine antibody comprising a coding tag with identifying information for phosphotyrosine antibody) is capable of binding to the polypeptide. If phosphotyrosine is present in the recording tag-labeled polypeptide, as illustrated, upon binding of the phosphotyrosine antibody to phosphotyrosine, the coding tag and recording tag anneal via complementary spacer sequences and the coding tag information is transferred to the recording tagto generate an extended recording tag. Figure 8B: An extended recording tag may comprise coding tag information for both primary amino acid sequence (e.g., "aai", "aa2", "aa3", ... , "aaN") and post- translational modifications (e.g., "PTMi", "PTM2") of the peptide. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0826] Figures 9A-B illustrate a process of multiple cycles of binding of a binding agent to an analyte (e.g., a macromolecule such as a polypeptide) and transferring information of a coding tag that is attached to a binding agent to an individual recording tag among a plurality of recording tags, for example, which are co-localized at a site of a single analyte attached to a solid support (e.g., a bead), thereby generating multiple extended recording tags that collectively represent the analyte information (e.g., presence or absence, level, or amount in a sample, binding profile to a library of binders, activity or reactivity, amino acid sequence, post-translational modification, sample origin, or any combination thereof). In this figure, for purposes of example only, the analyte is a polypeptide and each cycle involves binding a binding agent to an N-terminal amino acid (NTAA), recording the binding event by transferring coding tag information to a recording tag, followed by removal of the NTAA to expose a new NTAA. Figure 9A illustrates on a solid support a plurality of recording tags (e.g., comprising universal forward priming sequence and a UMI) which are available to a binding agent bound to the analyte. Individual recording tags possess a common spacer sequence (Sp) complementary to a common spacer sequence within coding tags of binding agents, which can be used to prime an extension reaction to transfer coding tag information to a recording tag. For example, the plurality of recording tags may co-localize with the analyte on the support, and some of the recording tags may be closer to the analyte than others. In one aspect, the density of recording tags relative to the analyte density on the support may be controlled, so that statistically each analyte will have a plurality of recording tags (e.g., at least about two, about five, about ten, about 20, about 50, about 100, about 200, about 500, about 1000, about 2000, about 5000, or more) available to a binding agent bound to that analyte. This mode may be particularly useful for analyzing low abundance proteins or polypeptides in a sample. Although Figure 9Ashows a different recording tag is extended in each of Cycles 1-3 (e.g., a cycle-specific barcode in the binding agent or separately added in each binding / reaction cycle may be used to "clock" the binding / reactions), it is envisaged that an extended recording tag may be further extended in any one or more of subsequent binding cycles, and the resultant pool of extended recording tags may be a mix of recording tags that are extended only once, twice, three times, or more. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0827] Figure 9B illustrates different pools of cycle-specific NTAA binding agents that are used for each successive cycle of binding, each pool having a cycle specific sequence, such as a cycle specific spacer sequence. Alternatively, the cycle specific sequence may be provided in a reagent separate from the binding agents. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0828] Figures lOA-C illustrate an exemplary mode comprising multiple cycles of transferring information of a coding tag that is attached to a binding agent to a recording tag among a plurality of recording tags co-localized at a site of a single analyte (e.g., a macromolecule such as a polypeptide) attached to a solid support (e.g., a bead), thereby generating multiple extended recording tags that collectively represent the analyte. In this figure, for purposes of example only, the analyte is a polypeptide and each round of processing involves binding to an NTAA, recording the binding event, followed by removal of the NTAA to expose a new NTAA. Figure 10Aillustrates a plurality of recording tags (e.g., comprising a universal forward priming sequence and a UMI) on a solid support for the analyte, for example, a single molecule per bead. Individual recording tags possess different spacer sequences at their 3 '-end with different "cycle specific" sequences (e.g., Ci, C2, C3, ... C«). For example, the recording tags on each bead share the samecompartment barcode and / or UMI sequence. In a first cycle of binding (Cycle 1), a plurality of NTAA binding agents is contacted with the analyte. The binding agents used in Cycle 1 possess a common 5'-spacer sequence (C 1) that is complementary to the Cycle 1 Ci spacer sequence of the recording tag. The binding agents used in Cycle 1 also possess a 3 '-spacer sequence (C'2) that is complementary to the Cycle 2 spacer C2. During binding Cycle 1, a first NTAA binding agent binds to the free N-terminus of the analyte, and the information of a first coding tag is transferred to a cognate recording tag via primer extension from the Ci sequence hybridized to the complementary C i spacer sequence. Following removal of the NTAA to expose a new NTAA, binding Cycle 2 contacts a plurality of NTAA binding agents that possess a Cycle 2 5'-spacer sequence (C'2) that is identical to the 3 '-spacer sequence of the Cycle 1 binding agents and a common Cycle 3 3 '-spacer sequence (C' 3), with the analyte. A second NTAA binding agent binds to the NTAA of the analyte, and the information of a second coding tag is transferred to a cognate recording tag via primer extension from the complementary C2 and C'2 spacer sequences. These cycles are repeated up to "«" binding cycles, wherein the last extended recording tag is capped with a universal reverse priming sequence, generating a plurality of extended recording tags co-localized with the single analyte, wherein each extended recording tag possesses coding tag information from one binding cycle. Because each set of binding agents used in each successive binding cycle possess cycle specific spacer sequences in the coding tags, binding cycle information can be associated with binding agent information in the resulting extended recording tags. Figure 10B illustrates different pools of cycle-specific binding agents that are used for each successive cycle of binding, each pool having cycle specific spacer sequences. Figure IOC illustrates how the collection of extended recording tags (e.g., that are co-localized at the site of the analyte) can be assembled in a sequential order based on PCR assembly of the extended recording tags using cycle specific spacer sequences, thereby providing an ordered sequence of the analyte such as a macromolecule. In a preferred mode, multiple copies of each extended recording tag are generated via amplification prior to concatenation. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a bindingcycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0829] Figures 11A-B illustrate information transfer from recording tag to a coding tag or di- tag construct. Two methods of recording binding information are illustrated in (A) and (B). A binding agent may be any type of binding agent as described herein; an anti-phosphotyrosine binding agent is shown for illustration purposes only. For extended coding tag or di-tagconstruction, rather than transferring binding information from the coding tag to the recording tag, information is either transferred from the recording tag to the coding tag to generate an extended coding tag (Figure 11 A), or information is transferred from both the recording tag and coding tag to a third di -tag-forming construct (Figure 11B). The di-tag and extended coding tag comprise the information of the recording tag (containing a barcode, an optional UMI sequence, and an optional compartment tag (CT) sequence (not illustrated)) and the coding tag. The di-tag and extended coding tag can be eluted from the recording tag, collected, and optionally amplified and read out on a next generation sequencer. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof {e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0830] Figures 12A-D illustrate design of PNA combinatorial barcode / UMI recording tag and di-tag detection of binding events. In Figure 12A, the construction of a combinatorial PNA barcode / UMI via chemical ligation of four elementary PNA word sequences (A, A'-B, B'-C, and C) is illustrated. Hybridizing DNA arms are included to create a spacer-less combinatorial template for combinatorial assembly of a PNA barcode / UMI. Chemical ligation is used to stitch the annealed PNA "words" together. Figure 12B shows a method to transfer the PNA information of the recording tag to a DNA intermediate. The DNA intermediate is capable of transferring information to the coding tag. Namely, complementary DNA word sequences are annealed to the PNA and chemically ligated (optionally enzymatically ligated if a ligase is discovered that uses a PNA template). In Figure 12C, the DNA intermediate is designed to interact with the coding tag via a spacer sequence, Sp. A strand-displacing primer extension step displaces the ligated DNA andtransfers the recording tag information from the DNA intermediate to the coding tag to generate an extended coding tag. A terminator nucleotide may be incorporated into the end of the DNA intermediate to prevent transfer of coding tag information to the DNA intermediate via primer extension. Figure 12D: Alternatively, information can be transferred from the coding tag to the DNA intermediate to generate a di-tag construct. A terminator nucleotide may be incorporated into the end of the coding tag to prevent transfer of recording tag information from the DNAintermediate to the coding tag. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0831] Figures 13A-E illustrate proteome partitioning on a compartment barcoded bead, and subsequent di-tag assembly via emulsion fusion PCR to generate a library of elements representing polypeptide sequence composition. The amino acid content of the polypeptide can be subsequently characterized through N-terminal sequencing or alternatively through attachment (covalent or non- covalent) of amino acid specific chemical labels or binding agents associated with a coding tag. The coding tag comprises universal priming sequence, as well as an encoder sequence for the amino acid identity, a compartment tag, and an amino acid UMI. After information transfer, the di-tags are mapped back to the originating molecule via the recording tag UMI. In Figure 13A, the proteome is compartmentalized into droplets with barcoded beads. Peptides with associated recording tags (comprising compartment barcode information) are attached to the bead surface. The droplet emulsion is broken, releasing barcoded beads with partitioned peptides. In Figure 13B, specific amino acid residues on the peptides are chemically labeled with DNA coding tags that are conjugated to site-specific labeling moieties. The DNA coding tags comprise amino acid barcode information and optionally an amino acid UMI. Figure 13C: Labeled peptide-recording tag complexes are released from the beads. Figure 13D: The labeled peptide-recording tag complexes are emulsified into nano or microemulsions such that there is, on average, less than one peptide- recording tag complex per compartment. Figure 13E: An emulsion fusion PCR transfers recording tag information (e.g., compartment barcode) to all of the DNA coding tags attached to the aminoacid residues. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc.), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0832] Figure 14 illustrates generation of extended coding tags from emulsified peptide recording tag -coding tags complex. The peptide complexes from Figure 13C are co-emulsified with PCR reagents into droplets with on average a single peptide complex per droplet. A three- primer fusion PCR approach is used to amplify the recording tag associated with the peptide, fuse the amplified recording tags to multiple binding agent coding tags or coding tags of covalently labeled amino acids, extend the coding tags via primer extension to transfer peptide UMI and compartment tag information from the recording tag to the coding tag, and amplify the resultant extended coding tags. There are multiple extended coding tag species per droplet, with a different species for each amino acid encoder sequence-UMI coding tag present. In this way, both the identity and count of amino acids within the peptide can be determined. The Ul universal primer and Sp primer are designed to have a higher melting Tmthan the U2tr universal primer. This enables a two-step PCR in which the first few cycles are performed at a higher annealing temperature to amplify the recording tag, and then stepped to a lower Tm so that the recording tags and coding tags prime on each other during PCR to produce an extended coding tag, and the Ul and U2tr universal primers are used to prime amplification of the resultant extended coding tag product. In certain embodiments, premature polymerase extension from the U2tr primer can be prevented by using a photo-labile 3 ' blocking group (Young et al., 2008, Chem. Commun. (Camb) 4:462-464). After the first round of PCR amplifying the recording tags, and a second-round fusion PCR step in which the coding tag Sptr primes extension of the coding tag on the amplified Sp' sequences of the recording tag, the 3 ' blocking group of U2tr is removed, and a higher temperature PCR is initiated for amplifying the extended coding tags with Ul and U2tr primers. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di-tag, the compartment tag, or the partition tag, if applicable), or any portion thereof (e.g., a universal primer, a spacer, a UMI, arecording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0833] Figure 15 illustrates use of proteome partitioning and barcoding facilitating enhanced mappability and phasing of proteins. In polypeptide sequencing, proteins are typically digested into peptides. In this process, information about the relationship between individual polypeptides that originated from a parent protein molecule, and their relationship to the parent protein molecule is lost. In order to reconstruct this information, individual peptide sequences are mapped back to a collection of protein sequences from which they may have derived. The task of finding a unique match in such a set is rendered more difficult with short and / or partial peptide sequences, and as the size and complexity of the collection {e.g., proteome sequence complexity) increases. The partitioning of the proteome into barcoded {e.g., compartment tagged) compartments or partitions, subsequent digestion of the protein into peptides, and the joining of the compartment tags to the peptides reduces the "protein" space to which a peptide sequence needs to be mapped to, greatly simplifying the task in the case of complex protein samples. Labeling of a protein with unique molecular identifier (UMI) prior to digestion into peptides facilitates mapping of peptides back to the originating protein molecule and allows annotation of phasing information between post- translational modified (PTM) variants derived from the same protein molecule and identification of individual proteoforms. Figure 15A shows an example of proteome partitioning comprising labeling proteins with recording tags comprising a compartment or partition barcode and subsequent fragmentation into recording-tag labeled peptides. Figure 15B: For partial peptide sequence information or even just composition information, this mapping is highly-degenerate. However, partial peptide sequence or composition information coupled with information from multiple peptides from the same protein, allow unique identification of the originating protein molecule. In any of the examples shown in this figure, the encoding tag and / or the recording tag (and / or the di- tag, the compartment tag, or the partition tag, if applicable), or any portion thereof {e.g., a universal primer, a spacer, a UMI, a recording tag barcode, an encoder sequence, a binding cycle-specific barcode, etc), may comprise or be replaced with a sequenceable polymer, such as a non-nucleic acid sequenceable polymer.

[0834] Figure 16 illustrates exemplary modes of compartment tagged bead sequence design. The compartment tags comprise a barcode of X5-20 to identify an individual compartment and a unique molecular identifier (UMI) of N5-10 to identify the peptide to which the compartment tag is joined, where X and N represent degenerate nucleobases or nucleobase words. Compartment tags can be single stranded (upper depictions) or d...

Claims

CLAIMS1. A method for analyzing a macromolecule, comprising the steps of:(a) providing a macromolecule and an associated recording polymer joined to a solid support;(b) contacting the macromolecule with a first binding agent capable of binding to the macromolecule, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(c) transferring the information of the first coding polymer to the recording polymer to generate a first order extended recording polymer;(d) contacting the macromolecule with a second binding agent capable of binding to the macromolecule, wherein the second binding agent comprises a second coding polymer with identifying information regarding the second binding agent;(e) transferring the information of the second coding polymer to the first order extended recording polymer to generate a second order extended recording polymer; and(f) analyzing the second order extended recording polymer.

2. The method of claim 1, wherein contacting steps (b) and (d) are performed in sequential order.

3. The method of claim 1, where wherein contacting steps (b) and (d) are performed at the same time.

4. The method of claim 1, further comprising, between steps (e) and (f), the following steps: (x) repeating steps (d) and (e) one or more times by replacing the second binding agent with a third (or higher order) binding agent capable of binding to the macromolecule, wherein the third (or higher order) binding agent comprises a third (or higher order) coding polymer with identifying information regarding the third (or higher order) bind agent; and (y) transferring the information of the third (or higher order) coding polymer to the second (or higher order) extended recording polymer to generate a third (or higher order) extended recording polymer;and wherein the third (or higher order) extended recording polymer is analyzed in step (f).

5. A method for analyzing a macromolecule, comprising the steps of:(a) providing a macromolecule, an associated first recording polymer and an associated second recording polymer joined to a solid support;(b) contacting the macromolecule with a first binding agent capable of binding to the macromolecule, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(c) transferring the information of the first coding polymer to the first recording polymer to generate a first extended recording polymer;(d) contacting the macromolecule with a second binding agent capable of binding to the macromolecule, wherein the second binding agent comprises a second coding polymer with identifying information regarding the second binding agent;(e) transferring the information of the second coding polymer to the second recording polymer to generate a second extended recording polymer; and(f) analyzing the first and second extended recording polymers.

6. The method of claim 5, wherein contacting steps (b) and (d) are performed in sequential order.

7. The method of claim 5, wherein contacting steps (b) and (d) are performed at the same time.

8. The method of claim 5, wherein step (a) further comprises providing an associated third (or higher odder) recording polymer joined to the solid support.

9. The method of claim 8, further comprising, between steps (e) and (f), the following steps:(x) repeating steps (d) and (e) one or more times by replacing the second binding agent with a third (or higher order) binding agent capable of binding to the macromolecule, wherein the third (or higher order) binding agent comprises a third (or higher order) coding polymer with identifying information regarding the third (or higher order) bind agent; and(y) transferring the information of the third (or higher order) coding polymer to the third (or higher order) recording polymer to generate a third (or higher order) extended recording polymer;and wherein the first, second and third (or higher order) extended recording polymers are analyzed in step (f).

10. The method of any one of claims 5-9, wherein the first coding polymer, second coding polymer, and any higher order coding polymers comprise a binding cycle specific spacer polymer sequence.

11. A method for analyzing a peptide, comprising the steps of:(a) providing a peptide and an associated recording polymer joined to a solid support;(b) modifying the N-terminal amino acid (NTAA) of the peptide with a chemical agent;(c) contacting the peptide with a first binding agent capable of binding to the modified NTAA, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(d) transferring the information of the first coding polymer to the recording polymer to generate an extended recording polymer; and(e) analyzing the extended recording polymer.

12. The method of claim 11, wherein step (c) further comprises contacting the peptide with a second (or higher order) binding agent comprising a second (or higher order) coding polymer with identifying information regarding the second (or higher order) binding agent, wherein the second (or higher order) binding agent is capable of binding to a modified NTAA other than the modified NTAA of step (b).

13. The method of claim 12, wherein contacting the peptide with the second (or higher order) binding agent occurs in sequential order following the peptide being contacted with the first binding agent.

14. The method of claim 12, wherein contacting the peptide with the second (or higher order) binding agent occurs simultaneously with the peptide being contacted with the first binding agent.

15. The method of any one of claims 11-14, wherein the chemical agent is anisothiocyanate derivative, 2,4-dinitrobenzenesulfonic (DNBS), 4-sulfonyl-2-nitrofluorobenzene(SNFB) l-fluoro-2,4-dinitrobenzene, dansyl chloride, 7-methoxycoumarin acetic acid, a thioacylation reagent, a thioacetylation reagent, or a thiobenzylation reagent.

16. A method for analyzing a peptide, comprising the steps of:(a) providing a peptide and an associated recording polymer joined to a solid support;(b) modifying the N-terminal amino acid (NTAA) of the peptide with a chemical agent to yield a modified NTAA;(c) contacting the peptide with a first binding agent capable of binding to the modified NTAA, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(d) transferring the information of the first coding polymer to the recording polymer to generate a first extended recording polymer;(e) removing the modified NTAA to expose a new NTAA;(f) modifying the new NTAA of the peptide with a chemical agent to yield a newly modified NTAA;(g) contacting the peptide with a second binding agent capable of binding to the newly modified NTAA, wherein the second binding agent comprises a second coding polymer with identifying information regarding the second binding agent;(h) transferring the information of the second coding polymer to the first extended recording polymer to generate a second extended recording polymer; and(i) analyzing the second extended recording polymer.

17. A method for analyzing a peptide, comprising the steps of:(a) providing a peptide and an associated recording polymer joined to a solid support;(b) contacting the peptide with a first binding agent capable of binding to the N-terminal amino acid (NTAA) of the peptide, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(c) transferring the information of the first coding polymer to the recording polymer to generate an extended recording polymer; and(d) analyzing the extended recording polymer.

18. The method of claim 17, wherein step (b) further comprises contacting the peptide with a second (or higher order) binding agent comprising a second (or higher order) coding polymer with identifying information regarding the second (or higher order) binding agent, wherein the second (or higher order) binding agent is capable of binding to a NTAA other than the NTAA of the peptide.

19. The method of claim 18, wherein contacting the peptide with the second (or higher order) binding agent occurs in sequential order following the peptide being contacted with the first binding agent.

20. The method of claim 18, wherein contacting the peptide with the second (or higher order) binding agent occurs simultaneously with the peptide being contacted with the first binding agent.

21. A method for analyzing a peptide, comprising the steps of:(a) providing a peptide and an associated recording polymer joined to a solid support;(b) contacting the peptide with a first binding agent capable of binding to the N-terminal amino acid (NTAA) of the peptide, wherein the first binding agent comprises a first coding polymer with identifying information regarding the first binding agent;(c) transferring the information of the first coding polymer to the recording polymer to generate a first extended recording polymer;(d) removing the NTAA to expose a new NTAA of the peptide;(e) contacting the peptide with a second binding agent capable of binding to the new NTAA, wherein the second binding agent comprises a second coding polymer with identifying information regarding the second binding agent;(h) transferring the information of the second coding polymer to the first extended recording polymer to generate a second extended recording polymer; and(i) analyzing the second extended recording polymer.

22. The method of any one of claims 1-10, wherein the macromolecule is a protein, polypeptide or peptide.

23. The method of any one of claims 1-10, wherein the macromolecule is a peptide.

24. The method of any one of claims 11-23, wherein the peptide is obtained by fragmenting a protein from a biological sample.

25. The method of any one of claims 1-10, wherein the macromolecule is a lipid, a carbohydrate, or a macrocycle.

26. The method of any one of claims 1-25, wherein the recording polymer comprises a DNA molecule, DNA with pseudo-complementary bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, a non-nucleic acid sequenceable polymer, e.g., a polysaccharide, a polypeptide, a peptide, or a polyamide, or a combination thereof.

27. The method of any one of claims 1-26, wherein the recording polymer comprises a universal priming site.

28. The method of claim 27, wherein the universal priming site comprises a priming site for amplification, sequencing, or both.

29. The method of claims 1-28, where the recording polymer comprises a unique molecule identifier (UMI).

30. The method of any one of claims 1-29, wherein the recording polymer comprises a barcode.

31. The method of any one of claims 1-30, wherein the recording polymer comprises a spacer polymer at its 3 '-terminus.

32. The method of claim any one of claims 1-31, wherein the macromolecule and the associated recording polymer are covalently joined to the solid support.

33. The method of any one of claims 1-32, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

34. The method of claim 33, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

35. The method of any one of claims 1-34, wherein a plurality of macromolecules and associated recording polymers are joined to a solid support.

36. The method of claim 35, wherein the plurality of macromolecules are spaced apart on the solid support at an average distance > 50 nm.

37. The method of any one of claims 1-36, wherein the binding agent is a polypeptide or protein.

38. The method of claim 37, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or a modified ClpS.

39. The method of any one of claims 1-38, wherein the binding agent is capable of selectively binding to the macromolecule.

40. The method of any one of claims 1-39, wherein the coding polymer comprises a DNA molecule, an RNA molecule, a BNA molecule, an XNA molecule, a LNA molecule, a PNA molecule, a γΡΝΑ molecule, a non-nucleic acid sequenceable polymer, e.g., a polysaccharide, a polypeptide, a peptide, or a polyamide, or a combination thereof.

41. The method of any one of claims 1-40, wherein the coding polymer comprises an encoder sequence.

42. The method of any one of claims 1-41, wherein the coding polymer further comprises a spacer polymer, a binding cycle specific sequence, a unique molecular identifier, a universal priming site, or any combination thereof.

43. The method of any one of claims 1-42, wherein the binding agent and the coding polymer are joined by a linker.

44. The method of claims 1-42, wherein the binding agent and the coding polymer are joined by a Spy Tag / Spy Catcher or SnoopTag / SnoopCatcher peptide-protein pair.

45. The method of any one of claims 1-44, wherein transferring the information of the coding polymer to the recording polymer is mediated by a DNA ligase.

46. The method of any one of claims 1-44, wherein transferring the information of the coding polymer to the recording polymer is mediated by a DNA polymerase.

47. The method of any one of claims 1-44, wherein transferring the information of the coding polymer to the recording polymer is mediated by chemical ligation.

48. The method of any one of claims 1-47, wherein analyzing the extended recording polymer comprises a nucleic acid sequencing method.

49. The method of claim 48, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

50. The method of claim 48, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

51. The method of any one of claims 1-50, wherein the extended recording polymer is amplified prior to analysis.

52. The method of claim 1-51, wherein the order of coding polymer information contained on the extended recording polymer provides information regarding the order of binding by the binding agents to the macromolecule.

53. The method of claim 1-52, wherein frequency of the coding polymer information contained on the extended recording polymer provides information regarding the frequency of binding by the binding agents to the macromolecule.

54. The method of claim 1-53, wherein a plurality of extended recording polymers representing a plurality of macromolecules are analyzed in parallel.

55. The method of claim 54, wherein the plurality of extended recording polymers representing a plurality of macromolecules is analyzed in a multiplexed assay.

56. The method of any one of claims 1-55, wherein the plurality of extended recording polymers undergoes a target enrichment assay prior to analysis.

57. The method of any one of claims 1-56, wherein the plurality of extended recording polymers undergoes a subtraction assay prior to analysis.

58. The method of any one of claims 1-57, wherein the plurality of extended recording polymers undergoes a normalization assay to reduce highly abundant species prior to analysis.

59. The method of any one of claims 1-58, wherein the NTAA is removed by a modified aminopeptidase, a modified amino acid tRNA synthetase, mild Edman degradation, Edmanase enzyme, or anhydrous TFA.

60. The method of any one of claims 1-59, wherein at least one binding agent binds to a terminal amino acid residue.

61. The method of any one of claims 1-60, wherein at least one binding agent binds to a post-translationally modified amino acid.

62. A method for analyzing one or more peptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising:(a) partitioning the plurality of protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags (e.g., in the form of non-nucleic acid sequenceable polymers) optionally joined to a solid support, wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments;(b) fragmenting the plurality of protein complexes, proteins, and / or polypeptides into a plurality of peptides;(c) contacting the plurality of peptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of peptides with the plurality ofcompartment tags within the plurality of compartments, thereby generating a plurality ofcompartment tagged peptides;(d) collecting the compartment tagged peptides from the plurality of compartments; and(e) analyzing one or more compartment tagged peptide according to a method of any one of claims 1-21 and 26-61.

63. The method of claim 62, wherein the compartment is a microfluidic droplet.

64. The method of claim 62, wherein the compartment is a microwell.

65. The method of claim 62, wherein the compartment is a separated region on a surface.

66. The method of any one of claims 62-65, wherein each compartment comprises on average a single cell.

67. A method for analyzing one or more peptides from a sample comprising a plurality of protein complexes, proteins, or polypeptides, the method comprising:(a) labeling of the plurality of protein complexes, proteins, or polypeptides with a plurality of universal DNA tags;(b) partitioning the plurality of labeled protein complexes, proteins, or polypeptides within the sample into a plurality of compartments, wherein each compartment comprises a plurality of compartment tags (e.g., in the form of non-nucleic acid sequenceable polymers), wherein the plurality of compartment tags are the same within an individual compartment and are different from the compartment tags of other compartments;(c) contacting the plurality of protein complexes, proteins, or polypeptides to the plurality of compartment tags under conditions sufficient to permit annealing or joining of the plurality of protein complexes, proteins, or polypeptides with the plurality of compartment tags within the plurality of compartments, thereby generating a plurality of compartment tagged protein complexes, proteins or polypeptides;(d) collecting the compartment tagged protein complexes, proteins, or polypeptides from the plurality of compartments;(e) optionally fragmenting the compartment tagged protein complexes, proteins, or polypeptides into a compartment tagged peptides; and(f) analyzing one or more compartment tagged peptide according to a method of any one of claims 1-21 and 26-61.

68. The method of any one of claims 62-67, wherein compartment tag information is transferred to a recording polymer associated with a peptide via primer extension or ligation.

69. The method of any one of claims 62-68, wherein the solid support comprises a bead.

70. The method of claim 69, wherein the bead is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

71. The method of any one of claims 62-70, wherein the compartment tag comprises a single stranded or double stranded nucleic acid molecule.

72. The method of any one of claims 62-71, wherein the compartment tag comprises a barcode and optionally a UMI.

73. The method of claim 72, wherein the solid support is a bead and the compartment tag comprises a barcode, further wherein beads comprising the plurality of compartment tags joined thereto are formed by split-and-pool synthesis.

74. The method of claim 72, wherein the solid support is a bead and the compartment tag comprises a barcode, further wherein beads comprising a plurality of compartment tags joined thereto are formed by individual synthesis or immobilization.

75. The method of any one of claims 62-74, wherein the compartment tag is a component within a recording polymer, wherein the recording polymer optionally further comprises a spacer polymer, a unique molecular identifier, a universal priming site, or any combination thereof.

76. The method of any one of claims 62-75, wherein the compartment tags further comprise a functional moiety capable of reacting with an internal amino acid or N-terminal amino acid on the plurality of protein complexes, proteins, or polypeptides.

77. The method of claim 76, wherein the functional moiety is an NHS group.

78. The method of claim 76, wherein the functional moiety is an aldehyde group.

79. The method of any one of claims 62-78, wherein the plurality of compartment tags is formed by: printing, spotting, ink-jetting the compartment tags into the compartment, or a combination thereof.

80. The method of any one of claims 62-79, wherein the compartment tag further comprises a peptide.

81. The method of claim 80, wherein the compartment tag peptide comprises a protein ligase recognition sequence.

82. The method of claim 81, wherein the protein ligase is butelase I or a homolog thereof.

83. The method of any one of claims 62-82, wherein the plurality of polypeptides is fragmented with a protease.

84. The method of claim 83, wherein the protease is a metalloprotease.

85. The method of claim 84, wherein the activity of the metalloprotease is modulated by photo-activated release of metallic cations.

86. The method of any one of claims 62-85, further comprising subtraction of one or more abundant proteins from the sample prior to partitioning the plurality of polypeptides into the plurality of compartments.

87. The method of claim 62-86, further comprising releasing the compartment tags from the solid support prior to joining of the plurality of peptides with the compartment tags.

88. The method of claim 62, further comprising following step (d), joining the compartment tagged peptides to a solid support in association with recording polymers.

89. The method of claim 88, further comprising transferring information of the compartment tag on the compartment tagged peptide to the associated recording polymer.

90. The method of claim 89, further comprising removing the compartment tags from the compartment tagged peptides prior to step (e).

91. The method of any one of claims 62-90, further comprising determining the identity of the single cell from which the analyzed peptide derived based on the analyzed peptide's compartment tag sequence.

92. The method of any one of claims 62-90, further comprising determining the identity of the protein or protein complex from which the analyzed peptide derived based on the analyzed peptide's compartment tag sequence.

93. A method for analyzing a plurality of macromolecules, comprising the steps of:(a) providing a plurality macromolecules and associated recording polymers joined to a solid support;(b) contacting the plurality of macromolecules with a plurality of binding agents capable of binding to the plurality of macromolecules, wherein each binding agent comprises a coding polymer with identifying information regarding the binding agent;(c) (i) transferring the information of the macromolecule associated recording polymers to the coding polymers of the binding agents that are bound to the macromolecules to generate extended coding polymers; or (ii) transferring the information of macromolecule associated recording polymers and coding polymers of the binding agents that are bound to the macromolecules to a di- tag construct;(d) collecting the extended coding polymers or di-tag constructs;(e) optionally repeating steps (b) - (d) for one or more binding cycles;(f) analyzing the collection of extended coding polymers or di-tag constructs.

94. The method of claim 93, wherein the macromolecule is a protein.

95. The method of claim 93, wherein the macromolecule is a peptide.

96. The method of claim 95, wherein the peptide is obtained by fragmenting a protein from a biological sample.

97. The method of any one of claims 93-96, wherein the recording polymer comprises a DNA molecule, an RNA molecule, a PNA molecule, a BNA molecule, an XNA, molecule, an LNA molecule, a γΡΝΑ molecule, a non-nucleic acid sequenceable polymer, e.g., a polysaccharide, a polypeptide, a peptide, or a polyamide, or a combination thereof.

98. The method of any one of claims 93-97, wherein the recording polymer comprises a unique molecular identifier (UMI) (e.g., in the form of a non-nucleic acid sequenceable polymer).

99. The method of claims 93-98, wherein the recording polymer comprises acompartment tag (e.g., in the form of a non-nucleic acid sequenceable polymer).

100. The method of any one of claims 93-99, wherein the recording polymer comprises a universal priming site (e.g., in the form of a non-nucleic acid sequenceable polymer).

101. The method of any one of claims 93-100, wherein the recording polymer comprises a spacer polymer at its 3 '-terminus, e.g., in the form of a non-nucleic acid sequenceable polymer.

102. The method of any one of claims 93-101, wherein the 3'-terminus of the recording polymer is blocked to prevent extension of the recording polymer by a polymerase and the information of macromolecule associated recording polymer and coding polymer of the bindingagent that is bound to the macromolecule is transferred to a di-tag construct (e.g., in the form of a non-nucleic acid sequenceable polymer).

103. The method of any one of claims 93-102, wherein the coding polymer comprises an encoder sequence.

104. The method of any one of claims 93-103, wherein the coding polymer comprises aUMI.

105. The method of any one of claims 93-104, wherein the coding polymer comprises a universal priming site.

106. The method of any one of claims 93-105, wherein the coding polymer comprises a spacer polymer at its 3 '-terminus.

107. The method of any one of claims 93-106, wherein the coding polymer comprises a binding cycle specific sequence.

108. The method of any one of claims 93-107, wherein the binding agent and the coding polymer are joined by a linker.

109. The method of any one of claims 93-108, wherein transferring information of the recording polymer to the coding polymer is effected by primer extension.

110. The method of any one of claims 93-108, wherein transferring information of the recording polymer to the coding polymer is effected by ligation.

111. The method of any one of claims 93-108, wherein the di-tag construct is generated by gap fill, primer extension, or both.

112. The method of any one of claims 93-97, 107, 108, and 111, wherein the di-tag molecule comprises a universal priming site derived from the recording polymer, a compartment tag derived from the recording polymer, a unique molecular identifier derived from the recording polymer, an optional spacer polymer derived from the recording polymer, an encoder sequence derived from the coding polymer, a unique molecular identifier derived from the coding polymer, an optional spacer polymer derived from the coding polymer, and a universal priming site derived from the coding polymer.

113. The method of any one of claims 93-112, wherein the macromolecule and the associated recording polymer are covalently joined to the solid support.

114. The method of claim 113, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

115. The method of claim 114, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

116. The method of any one of claims 93-115, wherein the binding agent is a polypeptide or protein.

117. The method of claim 116, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or an antibody or binding fragment thereof.

118. The method of any one of claims 95-117 wherein the binding agent binds to a single amino acid residue, a dipeptide, a tripeptide or a post-translational modification of the peptide.

119. The method of claim 118, wherein the binding agent binds to an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue.

120. The method of claim 118, wherein the binding agent binds to an N-terminal peptide, a C-terminal peptide, or an internal peptide.

121. The method of claim 119, wherein the binding agent binds to the N-terminal amino acid residue and the N-terminal amino acid residue is cleaved after each binding cycle.

122. The method of claim 119, wherein the binding agent binds to the C-terminal amino acid residue and the C-terminal amino acid residue is cleaved after each binding cycle.

123. The method of claim 121, wherein the N-terminal amino acid residue is cleaved via Edman degradation.

124. The method of claim 93, wherein the binding agent is a site-specific covalent label of an amino acid or post-translational modification.

125. The method of any one of claims 93-124, wherein following step (b), complexes comprising the macromolecule and associated binding agents are dissociated from the solid support and partitioned into an emulsion of droplets or microfluidic droplets.

126. The method of claim 125, wherein each microfluidic droplet, on average, comprises one complex comprising the macromolecule and the binding agents.

127. The method of claim 125 or 126, wherein the recording polymer is amplified prior to generating an extended coding polymer or di-tag construct.

128. The method of claim 125-127, wherein emulsion fusion PCR is used to transfer the recording polymer information to the coding polymer or to create a population of di-tag constructs.

129. The method of any one of claims 93-128, wherein the collection of extended coding polymers or di-tag constructs are amplified prior to analysis130. The method of any one of claims 93-129, wherein analyzing the collection of extended coding polymers or di-tag constructs comprises a nucleic acid sequencing method.

131. The method of claim 130, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

132. The method of claim 130, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

133. The method of claim 130, wherein a partial composition of the macromolecule is determined by analysis of a plurality of extended coding polymers or di-tag constructs using unique compartment tags and optionally UMIs.

134. The method of any one of claims 1-133, wherein the analysis step is performed with a sequencing method having a per base error rate of > 5%, > 10%, > 15%, > 20%, > 25%, or > 30%.

135. The method of any one of claims 1-134, wherein the identifying components of a coding polymer, recording polymer, or both comprise error correcting codes.

136. The method of claim 135, wherein the identifying components are selected from an encoder sequence, barcode, UMI, compartment tag, cycle specific sequence, or any combination thereof.

137. The method of claim 135 or 136, wherein the error correcting code is selected from Hamming code, Lee distance code, asymmetric Lee distance code, Reed-Solomon code, and Levenshtein-Tenengolts code.

138. The method of any one of claims 1-134, wherein the identifying components of a coding polymer, recording polymer, or both are capable of generating a unique current or ionic flux or optical signature, wherein the analysis step comprises detection of the unique current or ionic flux or optical signature in order to identify the identifying components.

139. The method of claim 138, wherein the identifying components are selected from an encoder sequence, barcode, UMI, compartment tag, cycle specific sequence, or any combination thereof.

140. A method for analyzing a plurality of macromolecules, comprising the steps of:(a) providing a plurality macromolecules and associated recording polymers joined to a solid support;(b) contacting the plurality of macromolecules with a plurality of binding agents capable of binding to cognate macromolecules, wherein each binding agent comprises a coding polymer with identifying information regarding the binding agent;(c) transferring the information of a first coding polymer of a first binding agent to a first recording polymer associated with the first macromolecule to generate a first order extended recording polymer, wherein the first binding agent binds to the first macromolecule;(d) contacting the plurality of macromolecules with the plurality of binding agents capable of binding to cognate macromolecules;(e) transferring the information of a second coding polymer of a second binding agent to the first order extended recording polymer to generate a second order extended recording polymer, wherein the second binding agent binds to the first macromolecule;(f) optionally repeating steps (d) - (e) for "n" binding cycles, wherein the information of each coding polymer of each binding agent that binds to the first macromolecule is transferred to the extended recording polymer generated from the previous binding cycle to generate an nth order extended recording polymer that represents the first macromolecule;(g) analyzing the nth order extended recording polymer.

141. The method of claim 140, wherein a plurality of nth order extended recording polymers that represent a plurality of macromolecules are generated and analyzed.

142. The method of claim 140 or 141, wherein the macromolecule is a protein.

143. The method of claim 142, wherein the macromolecule is a peptide.

144. The method of claim 143, wherein the peptide is obtained by fragmenting proteins from a biological sample.

145. The method of any one of claims 140-144, wherein the plurality of macromolecules comprises macromolecules from multiple, pooled samples.

146. The method of any one of claims 140-145, wherein the recording polymer comprises a DNA molecule, an RNA molecule, a PNA molecule, a BNA molecule, an XNA, molecule, an LNA molecule, a γΡΝΑ molecule, a non-nucleic acid sequenceable polymer, e.g., a polysaccharide, a polypeptide, a peptide, or a polyamide, or a combination thereof.

147. The method of any one of claims 140-146, wherein the recording polymer comprises a unique molecular identifier (UMI).

148. The method of claims 140-147, wherein the recording polymer comprises a compartment tag.

149. The method of any one of claims 140-148, wherein the recording polymer comprises a universal priming site.

150. The method of any one of claims 140-149, wherein the recording polymer comprises a spacer polymer at its 3 '-terminus.

151. The method of any one of claims 140-150, wherein the coding polymer comprises an encoder sequence.

152. The method of any one of claims 140-151, wherein the coding polymer comprises aUMI.

153. The method of any one of claims 140-152, wherein the coding polymer comprises a universal priming site.

154. The method of any one of claims 140-153, wherein the coding polymer comprises a spacer polymer at its 3 '-terminus.

155. The method of any one of claims 140-154, wherein the coding polymer comprises a binding cycle specific sequence.

156. The method of any one of claims 140-155, wherein the coding polymer comprises a unique molecular identifier.

157. The method of any one of claims 140-156, wherein the binding agent and the coding polymer are joined by a linker.

158. The method of any one of claims 140-157, wherein transferring information of the recording polymer to the coding polymer is mediated by primer extension.

159. The method of any one of claims 140-158, wherein transferring information of the recording polymer to the coding polymer is mediated by ligation.

160. The method of any one of claims 140-159, wherein the plurality of macromolecules, the associated recording polymers, or both are covalently joined to the solid support.

161. The method of any one of claims 140-160, wherein the solid support is a bead, a porous bead, a porous matrix, an array, a glass surface, a silicon surface, a plastic surface, a filter, a membrane, nylon, a silicon wafer chip, a flow through chip, a biochip including signal transducing electronics, a microtitre well, an ELISA plate, a spinning interferometry disc, a nitrocellulose membrane, a nitrocellulose-based polymer surface, a nanoparticle, or a microsphere.

162. The method of claim 161, wherein the solid support is a polystyrene bead, a polymer bead, an agarose bead, an acrylamide bead, a solid core bead, a porous bead, a paramagnetic bead, glass bead, or a controlled pore bead.

163. The method of any one of claims 140-162, wherein the binding agent is a polypeptide or protein.

164. The method of claim 163, wherein the binding agent is a modified aminopeptidase, a modified amino acyl tRNA synthetase, a modified anticalin, or an antibody or binding fragment thereof.

165. The method of any one of claims 142-164 wherein the binding agent binds to a single amino acid residue, a dipeptide, a tripeptide or a post-translational modification of the peptide.

166. The method of claim 165, wherein the binding agent binds to an N-terminal amino acid residue, a C-terminal amino acid residue, or an internal amino acid residue.

167. The method of claim 165, wherein the binding agent binds to an N-terminal peptide, a C-terminal peptide, or an internal peptide.

168. The method of any one of claims 142-164, wherein the binding agent binds to a chemical label of a modified N-terminal amino acid residue, a modified C-terminal amino acid residue, or a modified internal amino acid residue.

169. The method of claim 166 or 168, wherein the binding agent binds to the N-terminal amino acid residue or the chemical label of the modified N-terminal amino acid residue, and the N- terminal amino acid residue is cleaved after each binding cycle.

170. The method of claim 166 or 168, wherein the binding agent binds to the C-terminal amino acid residue or the chemical label of the modified C-terminal amino acid residue, and the C- terminal amino acid residue is cleaved after each binding cycle.

171. The method of claim 169, wherein the N-terminal amino acid residue is cleaved via Edman degradation, Edmanase, a modified amino peptidase, or a modified acylpeptide hydrolase.

172. The method of claim 163, wherein the binding agent is a site-specific covalent label of an amino acid or post-translational modification.

173. The method of any one of claims 140-172, wherein the plurality of nth order extended recording polymers are amplified prior to analysis.

174. The method of any one of claims 140-173, wherein analyzing the nth order extended recording polymer comprises a nucleic acid sequencing method.

175. The method of claim 174, wherein a plurality of nth order extended recording polymers representing a plurality of macromolecules are analyzed in parallel.

176. The method of claim 174 or 175, wherein the nucleic acid sequencing method is sequencing by synthesis, sequencing by ligation, sequencing by hybridization, polony sequencing, ion semiconductor sequencing, or pyrosequencing.

177. The method of claim 174 or 175, wherein the nucleic acid sequencing method is single molecule real-time sequencing, nanopore-based sequencing, or direct imaging of DNA using advanced microscopy.

178. A kit, comprising:(a) a recording polymer configured to associate directly or indirectly with an analyte;(b) (i) a coding polymer which comprises identifying information regarding a binding moiety capable of binding to the analyte, and which is configured to associate directly or indirectly with the binding moiety to form a binding agent, and / or (ii) a label,wherein the recording polymer and the coding polymer are configured to allow transfer of information between them, upon binding between the binding agent and the analyte; and optionally (c) the binding moiety.

179. A kit, comprising:at least (a) a first binding agent comprising (i) a first binding moiety capable of binding to an N-terminal amino acid (NTAA) or a functionalized NTAA of a polypeptide to be analyzed, and (ii) a first coding polymer comprising identifying information regarding the first binding moiety,optionally (b) a recording polymer configured to associate directly or indirectly with the polypeptide, andfurther optionally (c) a functionalizing reagent capable of modifying a first NTAA of the polypeptide to generate a first functionalized NTAA,wherein the recording polymer and the first binding agent are configured to allow transfer of information between the first coding polymer and the recording polymer, upon binding between the first binding agent and the polypeptide.

180. A kit, comprising:at least (a) one or more binding agents each comprising (i) a binding moiety capable of binding to an N-terminal amino acid (NTAA) or a functionalized NTAA of a polypeptide to be analyzed, and (ii) a coding polymer comprising identifying information regarding the binding moiety, and / or(b) one or more recording polymers configured to associate directly or indirectly with the polypeptide,wherein the one or more recording polymers and the one or more binding agents are configured to allow transfer of information between the coding polymers and the recording polymers, upon binding between each binding agent and the polypeptide, andoptionally (c) a functionalizing reagent capable of modifying a first NTAA of the polypeptide to generate a first functionalized NTAA.

181. A method, compri sing :(a) contacting a set of proteins, wherein each protein is associated directly or indirectly with a recording polymer, with a library of agents, wherein each agent comprises (i) a small molecule, a peptide or peptide mimetic, a peptidomimetic (e.g., a peptoid, a β-peptide, or a D- peptide peptidomimetic), a polysaccharide, or an aptamer (e.g., a nucleic acid aptamer, such as a DNA aptamer, or a peptide aptamer), and (ii) a coding polymer comprising identifying information regarding the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer,wherein each protein and / or its associated recording polymer, or each agent, is immobilized directly or indirectly to a support;(b) allowing transfer of information between (i) the recording polymer associated with each protein that binds and / or reacts with the small molecule(s), peptide(s) or peptide mimetic(s), peptidomimetic(s) (e.g., peptoid(s), P-peptide(s), or D-peptide peptidomimetic(s)), polysaccharide(s), or aptamer(s) of one or more agents, and (ii) the coding polymer of the one or more agents, to generate an extended recording polymer and / or an extended coding polymer; and(c) analyzing the extended recording polymer and / or the extended coding polymer.

182. A method for analyzing a polypeptide, comprising:(a) contacting (i) a set of fragments of a polypeptide, wherein each fragment is associated directly or indirectly with a recording polymer, with (ii) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding polymer comprising identifying information regarding the binding moiety,wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent, andwherein each fragment and / or its associated recording polymer, or each binding agent, is immobilized directly or indirectly to a support;(b) allowing transfer of information between (i) the recording polymer associated with each fragment and (ii) the coding polymer, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of the fragment, to generate an extended recording polymer and / or an extended coding polymer; and(c) analyzing the extended recording polymer and / or the extended coding polymer.

183. A method for analyzing a plurality of polypeptides, comprising:(a) labeling each molecule of a plurality of polypeptides with a plurality of universal tags;(b) contacting the plurality of polypeptides with a plurality of compartment tags(e.g., in the form of non-nucleic acid sequenceable polymers), under a condition suitable for annealing or joining of the plurality of universal tags with the plurality of compartment tags, thereby partitioning the plurality of polypeptides into a plurality of compartments (e.g., a bead surface, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof), wherein the plurality of compartment tags are the same within each compartment and are different from the compartment tags of other compartments;(c) fragmenting the polypeptide(s) in each compartment, thereby generating a set of polypeptide fragments each associated with a recording polymer comprising at least one universal polynucleotide tag and at least one compartment tag;(d) immobilizing the set of polypeptide fragments, directly or indirectly, to a support;(e) contacting the immobilized set of polypeptide fragments with a library of binding agents, wherein each binding agent comprises a binding moiety and a coding polymer comprising identifying information regarding the binding moiety,wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent;(f) allowing transfer of information between (i) the recording polymer associated with each fragment and (ii) the coding polymer, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of the fragment, to generate an extended recording polymer and / or an extended coding polymer; and(g) analyzing the extended recording polymer and / or the extended coding polymer.

184. A method for analyzing a plurality of polypeptides, comprising:(a) immobilizing a plurality of polypeptides to a plurality of substrates, wherein each substrate comprises a plurality of recording polymers each comprising a compartment tag, optionally wherein each compartment is a bead, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof;(b) fragmenting (e.g., by a protease digestion) the polypeptide(s) immobilized on each substrate, thereby generating a set of polypeptide fragments immobilized to the substrate;(c) contacting the immobilized set of polypeptide fragments with a library of binding agents, wherein each binding agent comprises a binding moiety and a coding polymer comprising identifying information regarding the binding moiety,wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C- terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent;(d) allowing transfer of information between (i) the recording polymer and (ii) the coding polymer, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of each fragment, to generate an extended recording polymer and / or an extended coding polymer; and(e) analyzing the extended recording polymer and / or the extended coding polymer.

185. A kit, comprising:(a) a library of agents, wherein each agent comprises (i) a small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, and / or aptamer, and (ii) a coding polymer comprising identifying information regarding the small molecule, peptide or peptide mimetic, peptidomimetic (e.g., peptoid, β-peptide, or D-peptide peptidomimetic), polysaccharide, or aptamer; andoptionally (b) a set of proteins, wherein each protein is associated directly or indirectly with a recording polymer,wherein each protein and / or its associated recording polymer, or each agent, is immobilized directly or indirectly to a support, andwherein the set of proteins, the recording polymers, and the library of agents are configured to allow information transfer between (i) the recording polymer associated with each protein that binds and / or reacts with the small molecule(s), peptide(s) or peptide mimetic(s), peptidomimetic(s) (e.g., peptoid(s), P-peptide(s), or D-peptide peptidomimetic(s)), polysaccharide(s), or aptamer(s) of one or more agents, and (ii) the coding polymer of the one or more agents, to generate an extended recording polymer and / or an extended coding polymer.

186. A kit for analyzing a polypeptide, comprising:(a) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding polymer comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acidsof the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent; andoptionally (b) a set of fragments of a polypeptide, wherein each fragment is associated directly or indirectly with a recording polymer, or (b') a means for fragmenting a polypeptide, such as a protease,wherein each fragment and / or its associated recording polymer, or each binding agent, is immobilized directly or indirectly to a support, andwherein the set of fragments of a polypeptide, the recording polymers, and the library of binding agents are configured to allow transfer of information between (i) the recording polymer associated with each fragment and (ii) the coding polymer, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of the fragment, to generate an extended recording polymer and / or an extended coding polymer.

187. A kit for analyzing a plurality of polypeptides, comprising: (a) a library of binding agents, wherein each binding agent comprises a binding moiety and a coding polymer comprising identifying information regarding the binding moiety, wherein the binding moiety is capable of binding to one or more N-terminal, internal, or C-terminal amino acids of the fragment, or capable of binding to the one or more N-terminal, internal, or C-terminal amino acids modified by a functionalizing reagent; and (b) a plurality of substrates, optionally with a plurality of polypeptides immobilized thereto, wherein each substrate comprises a plurality of recording polymers each comprising a compartment tag (e.g., in the form of a non-nucleic acid sequenceable polymer), optionally wherein each compartment is a bead, a microfluidic droplet, a microwell, or a separated region on a surface, or any combination thereof, wherein the polypeptide(s) immobilized on each substrate are configured to be fragmented (e.g., by a protease cleavage) to generate a set of polypeptide fragments immobilized to the substrate; wherein the plurality of polypeptides, the recording polymers, and the library of binding agents are configured to allow transfer of information between (i) the recording polymer and (ii) the coding polymer, upon binding between the binding moiety and the one or more N-terminal, internal, or C-terminal amino acids of each fragment, to generate an extended recording polymer and / or an extended coding polymer.

188. A method, comprising:(a) contacting an analyte with a first binding agent capable of binding to the analyte, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the analyte is associated with a recording portion joined to a support, and the analyte and / or the recording portion is immobilized to a support;(b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion;(c) contacting the analyte with a second binding agent capable of binding to the analyte, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent;(d) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and(e) analyzing the second order extended recording portion.

189. A method, comprising:(a) contacting a polypeptide with a first binding agent capable of binding to one or more N-terminal, internal, or C-terminal amino acid of the polypeptide, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the polypeptide is associated with a recording portion joined to a support, and the polypeptide and / or the recording portion is immobilized to a support;(b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion;(c) contacting the analyte with a second binding agent capable of binding to a different one or more N-terminal, internal, or C-terminal amino acid of the polypeptide, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent;(d) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and(e) analyzing the second order extended recording portion.

190. A method, comprising:(a) contacting a polypeptide with a first binding agent capable of binding to one or more N-terminal or C-terminal amino acid of the polypeptide, wherein the first binding agent comprises a first coding portion with identifying information regarding the first binding agent, the polypeptide is associated with a recording portion joined to a support, and the polypeptide and / or the recording portion is immobilized to a support;(b) transferring the information of the first coding portion to the recording portion to generate a first order extended recording portion;(c) eliminating the one or more N-terminal or C-terminal amino acid of the polypeptide, to expose a different one or more N-terminal or C-terminal amino acid of the polypeptide;(d) contacting the analyte with a second binding agent capable of binding to the different one or more N-terminal or C-terminal amino acid of the polypeptide, wherein the second binding agent comprises a second coding portion with identifying information regarding the second binding agent;(e) transferring the information of the second coding portion to the first order extended recording portion to generate a second order extended recording portion; and(f) analyzing the second order extended recording portion.

191. A kit, comprising any molecule, molecular complex or conjugate, reagent (e.g., chemical or biological), agent, structure (e.g., support, surface, particle, or bead), reaction intermediate, reaction product, binding complex, or any other article of manufacture disclosed and / or used in the method of claim 190.