Methods for site-specific conjugation of proteins containing glycosylated Fc domains - Patent Application 20070122999

Abstract

Provided herein is a method for site-specific conjugation of glycan-intact antibodies using transglutaminase. According to certain embodiments, the reaction conditions are maintained or reduced to low ionic strength conditions, which allow efficient and rapid conjugation without the need for antibody deglycosylation. Pharmaceutical compositions and uses related to the conjugation method are also described.

Description

[Technical Field]

[0001] (CROSS-REFERENCE TO RELATED APPLICATIONS) This application claims the benefit of priority to U.S. Provisional Application No. 63 / 027,400, filed May 20, 2020, which is incorporated herein by reference in its entirety for all purposes.

[0002] (Sequence Listing) This application contains a Sequence Listing that has been submitted electronically in ASCII format, and is incorporated herein by reference in its entirety. The ASCII copy, created on April 27, 2021, is named JBI6303WOPCT1_SL.txt and is 12,288 bytes in size.

[0003] FIELD OF THE INVENTION The present invention relates to a method for the site-specific conjugation of glycan-intact antibodies by transglutaminase under optimized buffer conditions to generate optimized antibody-drug-conjugates (ADCs) with better manufacturability and in vivo properties. [Background technology]

[0004] Covalent attachment of molecules to specific sites on large proteins, such as monoclonal antibodies (mAbs), is a technology of increasing importance. More and more therapeutic platforms that use site-specific conjugation, such as antibody-drug conjugates, are entering clinical development. As a result, novel methods to complement or replace existing approaches are of great value.

[0005] One approach to the site-specific conjugation described above utilizes transglutaminase (TGase) enzymes. Transglutaminases are a large class of enzymes found in microorganisms and higher organisms (Savoca et al., Micromachine (2018) 9(11):562). These enzymes catalyze the formation of covalent bonds between the ε-amino group of lysine and the γ-carboxamide group of the glutamine side chain of proteins, resulting in an isopeptide bond. TGases play a role in multiple biological processes, including blood coagulation, extracellular matrix assembly, and sporulation. In addition to their natural function, some TGases can substitute other amides or amines for glutamine or lysine side chains, respectively, thereby catalyzing the covalent conjugation of small molecule substrates to proteins. For example, they can conjugate the primary amine of a drug to the side chain carboxyamide group of a glutamine residue in a protein or peptide, forming an isopeptide bond between the drug and the protein or peptide.

[0006] Microbial TGase (MTG) from S. mobarensis has proven particularly useful for the covalent conjugation of small molecules to protein side chains. MTG has been shown to catalyze the addition of PEG to various proteins, including recombinant human IL2 (Sato, Advanced drug delivery reviews (2002), 54(4):487-504), interferon (Spolaore et al., Bioconjugate chemistry (2016), 27(11):2695-2706), and human growth hormone (Mero et al., J Control Release (2011), 154(1):27-34), by using amine-modified PEG for conjugation to the glutamine side chains of the protein or PEG modified with a Gln-containing dipeptide for conjugation to the lysine side chains of the protein. In both cases, PEG was selectively added to only one or a small subset of the Gln or Lys side chains. The substrate specificity of S. mobaraensis microbial TGase (MTG) is not fully understood, but various studies have shown some sequence selectivity for glutamine substrates (Sugimura et al., Arch Biochem Biophys (2008), 477(2):379-383) and some dependence on secondary structure (Spolaore et al., Biochemistry (2012), 51(43):8679-8689). Currently, empirical approaches are typically used to determine whether MTG can be used for the selective conjugation of specific proteins.

[0007] MTG has been used to selectively conjugate small molecules to monoclonal antibodies at specific sites. Two different approaches have been demonstrated for the conjugation of amine-containing payloads to Gln side chains on mAbs: one uses a tagging approach, and the other exploits the serendipitous discovery that certain Gln residues can be good MTG substrates under certain conditions. A tag-based approach for the conjugation of Gln-containing payloads to lysine side chains has also been described.

[0008] In the course of preparing radioimmunoconjugates, Jeger et al. demonstrated that the rate of modification of mAbs with MTG was much faster in deglycosylated antibodies than in those with intact N-linked glycans at Asn297 (Jeger et al., Angewandte Chemie (2010), 49(51):9995-9997), and that the modification was highly specific to one particular Gln site on the mAb. The conjugation site was identified as Gln295, which is conserved across all human IgG isotypes and is located in the CH2 domain, two residues upstream from the glycosylation site. Since then, deglycosylation followed by MTG-catalyzed conjugation to Gln295 has become a conventional approach for preparing antibody-radioconjugates, antibody-drug conjugates, and other molecules. While the MTG-driven conjugation method does not require antibody engineering, conjugation using this approach requires removal of the glycan at Asn297. Removal of the glycan at Asn297 has been shown to affect the immunological properties of antibodies, as binding to Fc receptors is abrogated, and also the biophysical properties of antibodies, as a decrease in thermal stability was observed following glycan removal, with a decrease in the melting temperature of the CH2 domain of up to 7–8°C.

[0009] A tag-based method for site-selective mAb conjugation with transglutaminase has also been demonstrated. It has been shown that adding or inserting a "Q-tag"—a short Gln-containing peptide such as LLQG—at a specific position in a mAb allows for selective conjugation with the tag without the need for deglycosylation (Strop et al., Chem Biol (2013), 20(2):161-167). A preferred approach has been to introduce Q-tags at the C-terminus of the mAb light and heavy chains by adding an exogenous peptide sequence. A similar approach has been described using the c-myc tag (Dennler et al., Chembiochem (2015), 16(5):861-867).

[0010] Site-specific conjugation has become an important area of ​​focus in the antibody-drug conjugate (ADC) field (Agarwal, P. and C.R. Bertozzi, Bioconjug Chem, (2015), 26(2):176-92), demonstrating that both the efficacy and safety of ADCs can be improved with site-specific methods compared to random conjugation. Summary of the Invention [Problem to be solved by the invention]

[0011] However, efficient methods for site-specific conjugation of antibodies that preserve the immunological and biophysical properties of the conjugated antibody, for example, preserving N-linked glycans and not introducing Gln-containing peptide tags, are still needed to generate safe and effective ADCs. [Means for solving the problem]

[0012] Provided herein are methods for site-specific conjugation of antibodies that do not require antibody deglycosylation. In some embodiments, the present invention provides a method for producing a conjugated antibody, the method comprising reacting a glycosylated antibody, a glycan-intact antibody, or an Fc-fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions.

[0013] In one aspect, a method for conjugating a glycosylated antibody is provided herein. One embodiment of the method includes contacting a glycan-intact antibody with a primary amine compound in the presence of transglutaminase under low ionic strength conditions that allow reaction of the primary amine with the antibody despite the presence of glycans. In some embodiments, the antibody is glycosylated. In some embodiments, the antibody is glycosylated at Asn297. The present disclosure is based on the discovery that low ionic strength buffer conditions allow conjugation of glycosylated antibodies without the need for the preliminary deglycosylation step required in conventional conjugation methods.

[0014] Embodiments of the method further include reducing the ionic strength of the transglutaminase preparation and / or antibody preparation prior to reacting with the amine compound to provide a low ionic strength transglutaminase preparation and / or antibody preparation. This additional step is preferred when the antibody and / or microbial transglutaminase preparation is provided in a high ionic strength buffer or contains unwanted additives that affect the rate of the transglutamination reaction.

[0015] In certain embodiments, the low ionic strength conditions include 10 mM or less sodium phosphate, potassium phosphate, sodium acetate, or Tris buffer. In another aspect, the degree of labeling (DOL) of the resulting conjugated antibody is at least 1.8. In some embodiments, the DOL is 2. [Brief explanation of the drawings]

[0016] The foregoing Summary of the Invention and the following Detailed Description of the Invention will be better understood when read in conjunction with the accompanying drawings. It is to be understood that the invention is not limited to the precise embodiments shown in the drawings. [Figure 1] Figure 1 shows the rate of MTG-catalyzed conjugation of 3-APA to intact, deglycosylated trastuzumab in different reaction buffer compositions. The degree of labeling (DOL) per heavy chain is shown as a function of time. [Figure 2A] Glycan-intact trastuzumab peptide mapping is shown. Trastuzumab was digested with trypsin and the peptides were analyzed by LC-MS. The peak corresponding to HC peptide 289-317 containing Gln295 glycosylation shows a retention time of 28.65 min. [Figure 2B] An enlarged version of the LC trace from 25 to 35 min is shown, highlighting the peak containing the Gln295 amino acid in the intact mAb. [Figure 2C] Peptide mapping of 3-APA-modified glycans of intact trastuzumab is shown. The 3-APA addition site was identified by trypsin digestion followed by LC-MS analysis. The peak corresponding to HC peptide 289-317 (retention time 28.65 min), which contains the glycosylated Gln295 site observed in the intact sample, is absent in the azide-conjugated sample and is replaced by a peptide corresponding to HC 289-317 (retention time 30.3 min) with a +83 Da modification at the Gln295 position. [Figure 2D] An enlarged version of the LC trace from 25 to 35 minutes is shown, highlighting the peak containing the Gln295 amino acid in the azide-conjugated antibody. [Figure 3A] 1 shows the melting temperatures of intact trastuzumab (glycosylated trastuzumab) compared to azido-conjugated trastuzumab produced by a low ionic strength method (glycosylated trastuzumab-3APA) and azido-conjugated trastuzumab produced by a deglycosylation method. [Figure 3B]1 shows the aggregation temperature of intact trastuzumab (glycosylated trastuzumab) compared to azide-conjugated trastuzumab produced by the low ionic strength method (glycosylated trastuzumab-3APA) and azide-conjugated trastuzumab produced by the deglycosylation method. [Figure 4] We compared the cell-killing activity of trastuzumab-Val-Cit-MMAF (T-vcMMAF) drug conjugates, generated by deglycosylated trastuzumab using an established transglutaminase method or under low-salt reaction conditions with glycan-intact mAb. SK-BR3 cells were treated with various concentrations of the conjugate for 72 hours, and cell killing was measured by the Cell Titer Glo assay. DETAILED DESCRIPTION OF THE INVENTION

[0017] Various publications, articles, and patents are cited or described in the Background and throughout this specification, and each of these references is incorporated herein by reference in its entirety. Any discussion of documents, operations, materials, devices, articles and the like which has been included in the specification is for the purpose of providing a context for the present invention. Such discussion is not an admission that any or all of these items constitute part of the prior art to any invention disclosed or claimed.

[0018] Throughout this specification, the numbering of amino acid residues in antibody constant regions is according to the EU index as set forth in Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, MD. (1991), unless otherwise expressly stated herein.

[0019] All references (including patent applications, patents, or literature) cited in this specification are incorporated herein by reference in their entirety for all purposes to the same extent as if each individual literature, patent, or patent application was specifically and individually indicated to be incorporated by reference in its entirety for all purposes.

[0020] term It should be understood that the terms used herein are used for the purpose of describing particular embodiments only and are not intended to be limiting. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used to carry out testing of the present invention, exemplary materials and methods are described herein. In describing and claiming the present invention, the following terms are used:

[0021] It should be noted that as used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "a cell" includes a combination of two or more cells, and the like.

[0022] Throughout this specification and the claims that follow, unless the context otherwise requires, the word "comprise" and variations such as "comprises" and "comprising" will be understood to mean the inclusion of the specified integer or step or group of integers or steps, but not the exclusion of any other integer or step or group of integers or steps. As used herein, the term "comprising" can be replaced with the terms "containing" or "including," or, as sometimes used herein, can also be replaced with the term "having."

[0023] The transitional phrases "comprising," "consisting essentially of," and "consisting" are intended to connote their generally accepted meanings in patent language, i.e., (i) "comprising" is synonymous with "comprising," "containing," or "characterized by" and is inclusive or open-ended, not excluding other unrecited elements or method steps; (ii) "consisting of" excludes any element, step, or ingredient not specified in the claim; and (iii) "consisting essentially of" limits the scope of the claim to the specified materials or steps and those that do not materially affect the "basic and novel characteristic(s)" of the claimed invention. Embodiments described with the phrase "comprising" (or its equivalents) are also provided as embodiments described independently with "consisting of" and "consisting essentially of."

[0024] As used herein, "consisting of" excludes any element, step, or ingredient not specified in the claim element. As used herein, "consisting essentially of" does not exclude materials or steps that do not materially affect the basic and novel characteristics of the claim. When used herein in connection with aspects or embodiments of the present invention, any of the above terms "comprising," "containing," "including," and "having" can be substituted with the terms "consisting of" or "essentially consisting of" to vary the scope of the disclosure.

[0025] As used herein, the connective term "and / or" between multiple listed elements is understood to encompass both individual and combined alternatives. For example, when two elements are connected by "and / or," the first alternative refers to the applicability of the first element without the second element. The second alternative refers to the applicability of the second element without the first element. The third alternative refers to the applicability of the first and second elements together. Any one of these alternatives is understood to be within the meaning and, therefore, meets the requirements of the term "and / or" as used herein. The simultaneous applicability of two or more of the alternatives is also understood to be within the meaning and, therefore, meets the requirements of the term "and / or."

[0026] An "antigen-binding fragment" or "antigen-binding domain" refers to a portion of a protein that binds to an antigen. Antigen-binding fragments may be synthetic, enzymatically obtainable, or genetically engineered polypeptides, and include antigen-binding portions of immunoglobulins, such as VH, VL, VH and VL, Fab, Fab', F(ab')2, Fd, and Fv fragments, domain antibodies (dAbs) consisting of one VH domain or one VL domain, shark variable IgNAR domains, camelized VH domains, VHH domains, minimal recognition units consisting of amino acid residues mimicking the CDRs of an antibody, such as the FR3-CDR3-FR4 portion, HCDR1, HCDR2, and / or HCDR3, and LCDR1, LCDR2, and / or LCDR3, alternative scaffolds that bind to antigen, and multispecific proteins comprising antigen-binding fragments. Antigen-binding fragments (such as VH and VL) can be linked together via synthetic linkers to form a variety of single-chain antibody designs in which, when the VH and VL domains are expressed as separate single chains, the VH / VL domains can pair intramolecularly or intermolecularly to form monovalent antigen-binding domains, e.g., single-chain Fvs (scFvs) or diabodies. Antigen-binding fragments can also be conjugated to other antibodies, proteins, antigen-binding fragments, or alternative scaffolds, which can be monospecific or multispecific, to engineer bispecific and multispecific proteins. As used herein, the term "antigen-binding fragment" refers to an antibody fragment such as, for example, a diabody, Fab, Fab', F(ab'), Fv fragment, disulfide-stabilized Fv fragment (dsFv), (dsFv)2, bispecific dsFv (dsFv-dsFv'), disulfide-stabilized diabody (dsdiabody), single-chain antibody molecule (scFv), single domain antibody (sdab), scFv dimers (bivalent diabodies), multispecific antibodies formed from a portion of an antibody comprising one or more CDRs, camelized single domain antibody, nanobody, domain antibody, bivalent domain antibody, or any other antibody fragment that binds to an antigen but does not comprise the entire antibody structure.An antigen-binding fragment can bind to the same antigen to which the parent antibody or parent antibody fragment binds.

[0027] As used herein, the term "single-chain antibody" refers to a single-chain antibody conventionally known in the art, which comprises a heavy-chain variable region and a light-chain variable region connected by a short peptide of about 15 to about 20 amino acids. As used herein, the term "single-domain antibody" refers to a single-domain antibody conventionally known in the art, which comprises a heavy-chain variable region and a heavy-chain constant region, or which comprises only a heavy-chain variable region.

[0028] As used herein, the term "antibody" or "immunoglobulin" is used broadly and includes immunoglobulin or antibody molecules, including polyclonal antibodies, monoclonal antibodies, including murine, human, human-adapted, humanized, and chimeric monoclonal antibodies, and antigen-binding fragments thereof.

[0029] In general, an antibody is a protein or peptide chain that exhibits binding specificity to a specific antigen, referred to herein as a "target." The structure of an antibody is known. An intact "antibody" comprises at least two heavy (H) chains and two light (L) chains interconnected by disulfide bonds. See generally, Fundamental Immunology, Ch. 7 (Paul, W., ed., 2nd ed. Raven Press, NY (1989)), incorporated by reference in its entirety for all purposes. Each heavy chain is composed of a heavy chain variable region (VH) and a heavy chain constant region (consisting of domains CH1, hinge, CH2, and CH3). Each light chain is composed of a light chain variable region (VL) and a light chain constant region (CL). The VH and VL regions can be further divided into hypervariable regions called complementarity-determining regions (CDRs), which are interspersed with framework regions (FR). Each VH and VL is composed of three CDR and four FR segments, arranged from amino-terminus to carboxy-terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, and FR4. Immunoglobulins can be assigned to five major classes, IgA, IgD, IgE, IgG, and IgM, depending on the amino acid sequence of the heavy chain constant domain. IgA and IgG are further classified into isotypes, IgA1, IgA2, IgG1, IgG2, IgG3, and IgG4. Antibody light chains of any vertebrate species can be assigned to one of two clearly distinct types, kappa (κ) and lambda (λ), based on the amino acid sequence of their constant domains. Thus, antibodies of the present invention can contain either a κ or λ light chain constant domain. According to certain embodiments, antibodies of the present invention comprise heavy and / or light chain constant regions of murine or human antibodies. Each of the four IgG subclasses has a distinct biological function, known as an effector function. These effector functions are generally mediated by interaction with Fc receptors (FcγR) or by binding of C1q and fixation of complement. Binding to FcγR can result in antibody-dependent cell-mediated cytolysis, whereas binding to complement factors can result in complement-mediated cytolysis.Antibodies useful in the present invention may have no or minimal effector functions but retain their ability to bind to FcRn. A "full-length antibody" is composed of two heavy chains (HC) and two light chains (LC), and multimers thereof (e.g., IgM), inter-connected by disulfide bonds.

[0030] The term "Fc fusion protein" refers to a fusion protein comprising at least one Fc polypeptide linked by a C-terminal or N-terminal fusion to a protein or peptide of interest, wherein the Fc polypeptide of the Fc fusion protein comprises IgG CH2 and IgG CH3 constant domain sequences.

[0031] As used herein, the term "engineered antibody" refers to an antibody or fragment thereof that comprises at least one engineered constant region, e.g., an engineered Fc region, an engineered Cκ region, and / or an engineered Cλ region. An engineered antibody can include one or more mutations, one or more amino acid residue deletions, or one or more amino acid insertions.

[0032] The term "glycan" refers to a polysaccharide or oligosaccharide. Glycan is also used to refer to the carbohydrate portion of a glycoconjugate, such as an antibody. O-linked and N-linked glycans are very common in eukaryotes. N-linked glycans are found attached to the R-group nitrogen (N) of asparagine in the Asn-X-Ser or Asn-X-Thr sequence, where X is any amino acid.

[0033] The term "exo-glycosidase" or "exoglycosidase" refers to an enzyme capable of hydrolyzing terminal glycosidic bonds in a glycan structure. Examples of suitable exo-glycosidases include, but are not limited to, sialidase, galactosidase, alpha-fucosidase, and alpha-mannosidase. The term "endo-glycosidase" or "endoglycosidase" refers to an enzyme capable of hydrolyzing glycosidic bonds between non-terminal residues in a glycan structure. Endo-glycosidases randomly hydrolyze glycan bonds from internal sites throughout the glycan. Examples include, but are not limited to, Endo-H, Endo-F3, Endo-F2, and Endo-F1.

[0034] The term "deglycosylated antibody" refers to an antibody in which the glycan group at N297 has been removed, thereby allowing Q295 to initiate conjugation with transglutaminase. Conventional conjugation methods known in the art provide methods that encompass this deglycosylation process to remove the glycan at N297 prior to conjugation with transglutaminase. A "glycosylated antibody" or a "glycosylated Fc fusion protein" refers to an antibody or Fc fusion protein, respectively, having an N-linked glycan at position N297 and / or other residues.

[0035] As used herein, the term "antibody glycan" refers to the N-linked glycan at position Asn297 in the Fc region of a monoclonal antibody heavy chain.

[0036] The term "glycan-intact antibody" or "intact antibody" or "native antibody" refers to an antibody molecule that has an intact glycan content and whose glycan content is unchanged compared to a native antibody. A glycan-intact antibody is an antibody whose glycans have not been hydrolyzed by endo- or exo-glycosidases (e.g., but not limited to, PNGase F or Endo F) or modified by glycan engineering (i.e., the antibody has not been "glycan engineered," such as by reducing the glycan or adding either natural or unnatural sugars to the glycan). In a glycan-intact antibody, a heterologous N-linked glycan is attached to asparagine at position 297 (N297) in the CH2 domain of the Fc region of the monoclonal antibody heavy chain.

[0037] The Fc region of IgG contains two glycans, one per heavy chain, attached to a single conserved glycosylation site at asparagine (Asn) 297. Each glycan can assume more than 30 different forms, a diversity that offers opportunities for fine-tuning humoral immunity. There are three major classes of glycans: G0, G1, and G2, depending on the number of terminal galactoses (0, 1, or 2). Complex-type oligosaccharides containing a core fucose in addition to a terminal galactose are described as G0F, G1F, and G2F (e.g., G2F refers to two terminal galactoses and a core fucose). Glycoforms lacking terminal galactose (designated G0, indicating 0 galactoses) are particularly pro-inflammatory because they have enhanced abilities to fix complement and engage the activating IgG receptor FcγRIIIa, while also blocking anti-inflammatory mechanisms mediated through sialylated and / or bigalactosylated (G2) glycans. Other small forms of glycans include G0F (no galactose, no bisecting N-acetylglucosamine, and core fucose) and G1F (galactose attached to either the α1,6 arm or the α1,3 arm).

[0038] The term "conjugated antibody" or "conjugate" refers to an antibody covalently attached to one or more chemical moieties, and the term "conjugated Fc-fusion protein" refers to an Fc-fusion protein covalently attached to one or more chemical moieties. The chemical moieties covalently attached to the antibody or Fc-fusion protein can include a linker, a reactive linker, an amine linker, a payload, a reactive payload, an amine payload, and / or a reactive linker-payload.

[0039] As used herein, the term "antibody-payload conjugate," "reactive payload," "conjugate," or "antibody drug conjugate" or "ADC" refers to an antibody or fragment thereof that is chemically linked to a cytotoxic or cytosolic drug / agent, toxin, or radionuclide, referred to herein as a "payload," and is capable of binding to a tumor-specific or tumor-associated cell surface antigen. Typically, antibody drug conjugates (ADCs) are formed by covalently attaching an anti-cancer drug to a mAb via a stable linker system. For example, tumor cell killing can occur when the drug conjugate binds to tumor cells and releases or / and enhances the cytotoxic activity of the drug moiety. The selectivity afforded by the drug conjugate minimizes toxicity to normal cells, thereby increasing the tolerability of the drug in patients.

[0040] In view of the present disclosure, any suitable payload known to one of skill in the art can be used in the present invention. The payload can be, for example, a drug / drug, a linker, a click reaction partner, etc. According to certain embodiments, the payload can be, for example, a cytotoxic drug, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, a linker, or a first click reaction partner.

[0041] As used herein, a "pharmaceutical composition" refers to a composition comprising at least one active pharmaceutical ingredient (API). Examples of APIs suitable for use in the present invention are conjugated antibodies or conjugated Fc-fusion proteins. Components other than the API in a pharmaceutical composition may include one or more excipients. Preferably, the excipients are substantially or completely pharmaceutically inactive.

[0042] As used herein, the term "covalently attached" means that the payload is attached to the antibody via at least one covalent bond. The attachment can be direct, i.e., without a linker, or indirect, i.e., via a linker.

[0043] As used herein, the term "linker" refers to a chemical moiety that connects two molecules. In view of the present disclosure, any suitable linker known to those of skill in the art can be used in the present invention. The linker can be, for example, a single covalent bond, a substituted or unsubstituted alkyl, a substituted or unsubstituted heteroalkyl moiety, a polyethylene glycol (PEG) linker, a peptide linker, a sugar-based linker, or a cleavable linker such as a disulfide bond or a protease cleavage site such as valine-citrulline-PAB.

[0044] As used herein, the term "amine-containing payload" refers to a payload containing one or more reactive amines (e.g., primary amines). For example, the amine-containing payload can include an amine donor unit (e.g., a primary amine NH), a linker (e.g., a molecule linked to the amine donor unit and having additional functionality for conjugation to a payload such as a small molecule, polypeptide, or biocompatible polymer), and a drug moiety (e.g., a payload such as a cytotoxic drug, cytostatic agent, chemotherapeutic agent, toxin, radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, unnatural amino acid, peptide, enzyme, fluorescent tag, biotin, linker, or first click reaction partner). The amine-containing payload can also be a polypeptide (e.g., an antibody) or biocompatible polymer containing one or more reactive lysines, N-termini, or reactive amines.

[0045] The term "drug-to-antibody ratio" or "DAR" refers to the number of drugs, e.g., 3-APA, conjugated to the antibody of an ADC. The number of drug molecules conjugated per antibody moiety, or the degree of labeling, is a parameter commonly used in the art and is referred to as "DAR," short for "drug-to-antibody ratio." The DAR of an ADC can range from 1 to 8, although higher loadings, e.g., 10, are possible depending on the number of binding sites on the antibody. The term DAR can be used to refer to the number of drugs loaded onto an individual antibody. A DAR of 2 indicates a drug-loaded species of two. The behavior of the DAR in biological samples indicates the stability of the ADC. A decrease in the DAR between two samples indicates the stability of the ADC.

[0046] The term "DOL" or "degree of labeling" refers to the number of covalently conjugated labels, such as 3-APA, per antibody heavy chain of an antibody-drug conjugate (ADC). The DOL can range from 1 to 8, although higher loadings, such as 10, are possible depending on the number of binding sites on the antibody. The term DOL can be used in reference to the number of drugs loaded onto an individual antibody. A DOL of 2 refers to a degree of labeling of 2. The degree of labeling is a parameter commonly used in the art. The terms "degree of substitution" or "DOS" can be used interchangeably with DOL. The degree of labeling is experimentally measured by mass spectrometry, UV-Vis spectroscopy, or chromatographic methods such as reverse-phase HPLC and hydrophobic interaction chromatography. The desired DOL for site-specific labeling methods is often complete occupancy of the desired site with the label absent from other sites. For example, for a typical antibody comprising two heavy chains and two light chains, each heavy chain containing a Gln295 conjugation site, the optimal DOL is a DOL of 2, in which both Gln295 residues of the antibody are fully conjugated to the drug molecule.

[0047] The term "reactive group" refers to a group that is capable of reacting with another chemical group to form a covalent bond, i.e., is covalently reactive under suitable reaction conditions, and generally represents a point of attachment for another substance.

[0048] The term "low ionic strength" or "low salt" conditions refers to buffer conditions in which the salt concentration of the buffer is maintained or made to be less than about 30 mM (also referred to herein as a "low ionic strength solution"). The salt can be a sodium salt, a potassium salt, or any other salt. A low salt concentration can be about 25 mM or less, or about 24 mM or less, or about 23 mM or less, or about 22 mM or less, or about 21 mM or less, or about 20 mM or less, or about 19 mM or less, or about 18 mM or less, or about 17 mM or less, or about 16 mM or less, or about 15 mM or less, or about 14 mM or less, or about 13 mM or less, or about 12 mM or less, or about 11.2 mM or less, or about 11 mM or less, or about 10 mM or less. The low salt concentration can be, for example, about 0.1 mM to about 10 mM, or about 1 mM to about 10 mM, or about 2 mM to about 10 mM, or about 0.1 mM to about 12 mM, or about 1 mM to about 12 mM, or about 2 mM to about 12 mM. The low salt concentration can be, for example, 25 mM, 24 mM, 23 mM, 22 mM, 21 mM, 20 mM, 19 mM, 18 mM, 17 mM, 16 mM, 15 mM, 14 mM, 13 mM, 12 mM, 11 mM, 10 mM, 9 mM, 8 mM, 7 mM, 6 mM, 5 mM, 4 mM, 3 mM, 2 mM, 1 mM, or 0 mM. Low salt or low ionic strength conditions can be achieved, for example, but not limited to, by dilution or buffer exchange methods such as dialysis, diafiltration, filtration, precipitation, and / or chromatography methods, and / or other methods such as precipitation or lyophilization. Methods that "reduce the ionic strength" of a solution or preparation refer to reducing the salt concentration of the solution or preparation.

[0049] "Tm" or "midpoint temperature" is the temperature midpoint of a thermal denaturation curve. It refers to the temperature at which 50% of the amino acid sequence is in its native conformation and the other 50% is denatured. Thermal denaturation curves are typically plotted as a function of temperature. Tm is used to measure protein stability. Generally, a higher Tm is indicative of a more stable protein. Tm can be easily measured using methods well known to those skilled in the art, such as circular dichroism spectroscopy, differential scanning calorimetry, differential scanning fluorometry (both intrinsic and extrinsic dye-based), UV spectroscopy, FT-IR, and isothermal calorimetry (ITC).

[0050] "Tagg" refers to the temperature at which a protein begins to aggregate through either dimerization or oligomerization. The aggregation temperature is the temperature at which the onset of aggregation is detected and indicates the tendency of a protein to aggregate. Tagg can be measured by differential scanning calorimetry (DSC), differential scanning fluorometry (DSF), or circular dichroism (CD). These techniques can detect small changes in protein conformation and therefore the onset of aggregation. The Tagg value can be lower or higher than Tm. If Tagg is lower than Tm, the protein will first dimerize and / or oligomerize, and then begin to unfold later at temperatures higher than Tagg. If Tagg is higher than Tm, the protein will first begin to unfold, and then aggregate at temperatures higher than Tm. Both events are commonly observed and depend on the amino acid composition and protein conformation.

[0051] As used herein, "Q295" or "Gln295" refers to an Fc conjugation site found in the CH2 domain of an antibody constant region. Gln295 is a substrate for transglutaminase. Because certain antibodies have two heavy chains and two Gln295 residues, transglutaminase antibody conjugation can provide antibodies with conjugates on each Gln295 residue with a drug-to-antibody ratio (DAR) of up to 2.0. Conjugation occurs between glutamine and an amine-conjugated payload. The bond between glutamine and an amine-containing payload is an isopeptide bond of the formula CO-NH-, where NH- is attached to the linker and payload moieties.

[0052] "N297" or "Asn297" refers to the heavy chain Fc glycosylation site. In traditional conjugation methods using microbial transglutaminase, this site is deglycosylated prior to conjugation.

[0053] As used herein, the term "transglutaminase" refers to an enzyme that catalyzes the formation of an isopeptide bond between a free amine group on a payload in an antibody or antigen-binding fragment thereof and an acyl group on the side chain of a glutamine residue. Transglutaminase is a protein-glutamine γ-glutamyltransferase (EC 2.3.2.13) that typically catalyzes the pH-dependent transamidation of glutamine residues with lysine residues. Examples of transglutaminases include, but are not limited to, microbial transglutaminase (mTG), human transglutaminase, tissue transglutaminase (tTG), and factor XIII. Examples of human transglutaminase include, but are not limited to, keratinocyte transglutaminase (Uniprot P22735), tissue transglutaminase (UniProt P21980), epidermal transglutaminase, and prostate transglutaminase. These enzymes may be derived from natural or recombinant sources. Glutamine and lysine amino acids in peptides or polypeptides can be substrates for transglutaminase cross-linking, for example, a payload can be linked to a linker containing lysine.

[0054] The transglutaminase may be any transglutaminase deemed suitable by those skilled in the art. The transglutaminase used in the invention described herein may be obtained or produced from a variety of sources. In some embodiments, the transglutaminase is a calcium-dependent transglutaminase that requires calcium to induce a conformational change in the enzyme to enable enzymatic activity. For example, transglutaminase derived from guinea pig liver can be obtained from commercial sources (e.g., Sigma-Aldrich (St. Louis, MO) and MP Biomedical (Irvine, CA)).

[0055] In some embodiments, the transglutaminase is derived from a fungal protein (e.g., Oomycetes, Actinomycetes, Saccharomyces, Candida, Cryptococcus, Monascus, or Rhizopus transglutaminases). In some embodiments, the transglutaminase polypeptide is derived from a slime mold (e.g., Physarum polycephalum transglutaminase). In some embodiments, the mTGase polypeptide is derived from a bacterial protein, such as a transglutaminase from the genus Streptoverticillium or Streptomyces (e.g., Streptomyces mobarensis or Streptoverticillium mobarensis).In some embodiments, the transglutaminase polypeptide is selected from the group consisting of Streptoverticillium mobarensis, Streptoverticillium griseocameum, Streptoverticillium ladakanum, Streptomyces mobarensis, Streptomyces viridis, Streptomyces ladakanum, Streptomyces caniferus, Streptomyces hygroscopius, Streptomyces hygroscopicus, Streptomyces netropsis, and the like. netropsis, Streptomyces lavendulae, Streptomyces roseovertivillatus, Streptomyces cinnamaoneous, Streptomyces griseocameum, Streptomyces lavendulae, Streptomyces lividans, Streptomyces lydicus, Streptomyces sioyansis, Actinomadura sp., Bacillus spp. (e.g., Bacillus circulans, Bacillus subtilis, etc.), Corynebacterium ammoniac, Corynebacterium glutamicum, Clostridium, Enterobacter species.The transglutaminase polypeptide is derived from a bacterial protein, such as a protein of Micrococcus sp., Providencia sp., or an isolate thereof. In some embodiments, the transglutaminase is a calcium-independent transglutaminase that does not require calcium to induce a conformational change in the enzyme to enable enzymatic activity. In some embodiments, the transglutaminase polypeptide is derived from S. mobaraensis.

[0056] Commercially available calcium-independent transglutaminases, such as ACTIVA (Ajinomoto), are also suitable for the present invention. In some embodiments, the transglutaminase used in the present invention described herein may also be a recombinant protein produced using recombinant techniques known to those skilled in the art. In some embodiments, the transglutaminase used in the present invention described herein may be a purified protein.

[0057] Throughout this specification, the numbering of amino acid residues in antibody constant regions is according to the EU index as set forth in Kabat et al. (1991, J Immunol 147(5):1709-19), unless expressly stated otherwise.

[0058] Conventional one-letter and three-letter amino acid codes are used herein as shown in Table 1.

[0059] [Table 1]

[0060] Methods of the Invention To assist the reader of this application, the description has been divided into various paragraphs or sections or directed to various embodiments of this application. These separations should not be considered as separating the substance of a paragraph or section or embodiment from the substance of another paragraph or section or embodiment. To the contrary, those skilled in the art will understand that the description herein has broad applicability and encompasses all combinations of the various paragraphs, paragraphs, and sentences that may be conceived.

[0061] The embodiments of the present invention are intended to be illustrative only, and those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific procedures of the invention. All such equivalents are considered to be within the scope of this invention and covered by the following claims.

[0062] Monoclonal antibodies (mAbs) are increasingly being used for targeted drug delivery due to their high selectivity for tumor-associated antigens, favorable pharmacokinetics, and relatively low inherent toxicity. Antibody-drug conjugates (ADCs) are formed by covalently attaching anticancer drugs to mAbs, usually via stable linker systems to specific sites on the mAb. Glutamine 295 (Q295), located in the CH2 domain of the Fc heavy chain of mAbs, is a commonly used conjugation site. Conjugation is typically performed using microbial transglutaminase (MTG), which catalyzes the formation of a stable isopeptide bond between the glutamine side chain and the free amine of the cytotoxic drug.

[0063] A major challenge in ADC manufacturing is the attachment of cytotoxic agents to antibodies in a manner that allows for strict control over the conjugation site, conjugation rate, and degree of labeling (DOL). The conjugation product is often a highly heterogeneous mixture with respect to its DOL, which not only complicates ADC development but can also result in a suboptimal therapeutic window for the final drug.

[0064] Antibodies are often glycosylated at residue N297, near the Q295 conjugation site. Removal of antibody glycans is known to increase the mobility of the C'D / E chain, as demonstrated by HD exchange (Houde D. et al., Anal Chem (2009), 81(7):2644). Furthermore, reactivity with MTG has been shown to correlate with protease susceptibility (Spolaore et al., 2012, Biochemistry 51(43):8679-8689) and is likely an indicator of backbone flexibility. Steric effects of the glycan molecule at N297 are thought to hinder conjugation at Q295. Glycosylation at residue N297 may hinder transglutaminase conjugation at Q295, affecting the degree of labeling (DOL) or drug-to-antibody ratio (DAR). As a result, conjugation of glycan-intact antibodies under conventional buffer conditions produces products with low labeling and efficacy.

[0065] In a conventional conjugation method known in the art, antibodies are deglycosylated or non-glycosylated at N297 to allow conjugation at Q295. The resulting antibody is suitable for treatment with microbial transglutaminase (MTG) without interfering with glycosylation and can be reacted with primary amine compounds to produce glutamyl-modified antibodies.

[0066] Conventional conjugation methods require an initial deglycosylation step, resulting in less manufacturable antibodies because removal of glycans inhibits antibody-Fc receptor interaction. Fc glycans are important for maintaining structural integrity, Fc receptor communication, and downstream immunological responses. The presence and structure of N-linked glycans, particularly at N297, are understood to be necessary for immune complexes to activate effector functions. Conjugated antibodies produced by conventional conjugation methods requiring deglycosylated or glycan-engineered antibodies typically have low activity and / or stability due to their glycan modification content. For example, the antibodies may lack stability, affinity, or selectivity.

[0067] The invention described herein provides a method for conjugating glycosylated antibodies, thus enabling the production of antibody-drug conjugates that are more suitable for manufacturing. The invention provides a desired DOL and provides conditions that are applicable to any reactive species or antibody. The conditions of the invention do not require glycan engineering or glycan removal.

[0068] Conventional microbial transglutaminase conjugation methods using deglycosylated or glycan-engineered antibodies are generally performed under conventional buffer conditions, such as PBS or a buffer with similar ionic strength. Existing methods used to adjust the degree of labeling (DOL) generally rely on varying the concentration of the carrier molecule or the reactive labeling species. The DOL can also vary depending on the chemical nature of the reactive species. However, such variations typically have little effect on the DOL when used with glycan-intact antibodies. In contrast to known procedures, the low ionic strength conditions of the present invention enable site-specific conjugation of antibodies with amine compounds or amine-containing payloads using transglutaminase, providing the desired DOL without the need for a preliminary deglycosylation step and removal of antibody glycans, thus enabling antibody-drug conjugates with better manufacturability.

[0069] In some embodiments, the primary amine compound comprises a reactive group that can be further reacted after transglutamation. In some embodiments, the glutamyl-modified antibody can be reacted with a reactive payload compound to form an antibody-payload conjugate. In some embodiments, the primary amine compound comprises an azide.

[0070] In some embodiments, the methods of the present invention provide improved recovery due to the elimination of the need for deglycosylation and subsequent purification, as well as the fact that deglycosylation improves the T of antibodies. m and T aggThis method may offer many advantages over conventional conjugation methods, including improved stability as it has been shown to reduce the levels of

[0071] In certain embodiments, the present invention provides a method for producing a conjugated antibody or a conjugated Fc-fusion protein, the method comprising reacting a glycosylated antibody or a glycosylated Fc-fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. The glycosylated antibody or glycosylated Fc-fusion protein comprises an N-linked glycan at amino acid Asn297. Preferably, the glycosylated antibody or glycosylated Fc-fusion protein has an intact glycan content. Preferably, the glycosylated antibody or glycosylated Fc-fusion protein has not been treated with an endo- or exo-glycosidase before reacting the glycosylated antibody or glycosylated Fc-fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. Preferably, the glycosylation site of the glycosylated antibody or glycosylated Fc fusion protein has not been glycan engineered or glycan modified prior to reacting the glycosylated antibody or glycosylated Fc fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions.

[0072] In certain embodiments, the antibodies used in the methods of the invention are glycosylated antibodies or glycosylated Fc fusion proteins, which have partially modified or partially engineered glycans but still retain an N-linked glycan at amino acid Asn297.

[0073] According to some embodiments, the glycosylated antibody has G0F, G1F, G2F, G0, G1, or G2 glycans.

[0074] In some embodiments, the antibody can be any antibody from those known to those of skill in the art. In some embodiments, the antibody comprises an IgA1, IgA2, IgD, IgE, IgG1, IgG2, IgG3, IgG4, or IgM heavy chain. In some embodiments, the antibody comprises a κ or λ light chain. In some embodiments, the antibody is a monoclonal antibody. In some embodiments, the antibody is a polyclonal antibody. In some embodiments, the antibody is a bispecific or multispecific antibody. In some embodiments, the antibody is a chimeric, humanized, or human antibody.

[0075] In some embodiments, the amine compound is an amine-containing payload comprising one or more of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, an imaging agent, or a first click reaction partner.

[0076] In some embodiments, the method of producing a conjugated antibody or conjugated Fc-fusion protein under low ionic strength conditions is carried out in a solution having a salt concentration of about 25 mM or less, or about 20 mM or less, or about 15 mM or less, or about 10 mM or less.

[0077] In another embodiment of the invention, the conjugation reaction is carried out in water buffered with, but not limited to, phosphate, acetate, or Tris. In an alternative embodiment, the low ionic strength solution comprises sodium phosphate, potassium phosphate, HEPES, sodium acetate, or Tris.

[0078] In some embodiments of the invention, the conjugation reaction is carried out under low ionic strength conditions containing up to 10 mM sodium phosphate, potassium phosphate, sodium acetate, or Tris.

[0079] In certain embodiments of the invention, the conjugation reaction is carried out under low ionic strength conditions comprising up to 10 mM potassium phosphate, up to 10 mM sodium phosphate, up to 10 mM sodium acetate, or up to 10 mM Tris.

[0080] In another embodiment of the invention, the method further comprises reducing the ionic strength of the antibody or antibody preparation prior to reacting with the amine compound to provide a low ionic strength antibody preparation, i.e., the method of producing a conjugated antibody or conjugated Fc-fusion protein comprises reducing the ionic strength of a solution containing a glycosylated antibody or glycosylated Fc-fusion protein to provide low ionic strength conditions.

[0081] In another embodiment of the present invention, the method further comprises reducing the ionic strength of the transglutaminase preparation prior to reacting with the amine compound to provide a low ionic strength transglutaminase preparation, i.e., the method for producing a conjugated antibody or conjugated Fc-fusion protein further comprises reducing the ionic strength of the solution containing the transglutaminase to provide low ionic strength conditions.

[0082] In another embodiment, the ionic strength is reduced by dilution or by dialysis, diafiltration, filtration, precipitation, and / or buffer exchange by chromatographic methods. In conjugation method embodiments, salts and / or additives are removed, for example, by dilution or by methods such as dialysis, diafiltration, filtration, precipitation, and / or buffer exchange by suitable chromatographic methods, including gel permeation, size exclusion chromatography, ion exchange chromatography, or affinity chromatography. Salt and / or additive removal can be achieved using dialysis membrane tubing, centrifugation devices with porous membranes sized to retain the protein but allow the buffer to pass through, and / or chromatographic supports. Alternatively or additionally, salt and / or additive removal can be by precipitation or lyophilization. The concentration of salts or additives is preferably reduced before the conjugation reaction begins. Ideally, the concentration of salts and / or additives is reduced to a level that allows conjugation of the conjugate without removing and / or manipulating the glycan content of the antibody. Ideally, the concentration of salts and / or additives is reduced to a level where greater than 90% of the antibody is conjugated to one amine-containing payload per heavy chain.

[0083] According to one embodiment, a method for producing a conjugated antibody or conjugated Fc-fusion protein comprises reacting a glycosylated antibody or glycosylated Fc-fusion protein with an amine compound in the presence of transglutaminase under conditions of low ionic strength sufficient to convert 80-100% or 90-100% of the glycosylated antibody or glycosylated Fc-fusion protein, respectively, to an antibody or Fc-fusion protein conjugated to one amine-containing payload per heavy chain (e.g., 2 DOL).

[0084] In other embodiments of the present invention, the transglutaminase is a microbial transglutaminase.As mentioned above, the transglutaminase can be any transglutaminase deemed suitable by the person skilled in the art.

[0085] In some embodiments of the present invention, the reaction is carried out for at least 18 hours.

[0086] In another embodiment of the invention, the reaction is carried out for at least 24 hours.

[0087] In certain embodiments, the amine compound is a primary amine compound containing an azide. In some embodiments, the primary amine compound contains a reactive group or a protected reactive group. The reactive group and the protected reactive group can be any group deemed suitable by those skilled in the art. In some embodiments, the reactive group can form a covalent bond with a reactive payload compound. Useful reactive groups include azide, alkyne, cycloalkyne, thiol, alcohol, ketone, aldehyde, acid, ester, hydrazide, aniline, tetrazine, cyclooctene, and cyclopropene. In certain embodiments, the primary amine group contains a carboxyl and the reactive payload contains an amine.

[0088] In another embodiment, the method further comprises reacting the conjugated antibody with a reactive payload compound to form an antibody-payload conjugate. The payload of the reactive payload compound can be any payload deemed suitable by those skilled in the art. In certain embodiments, the payload is provided in the form of a reactive payload compound containing a reactive group capable of forming a covalent bond with a reactive group on a primary amine compound. Reactive groups on reactive payload compounds include azides, alkynes, cycloalkynes, thiols, alcohols, ketones, aldehydes, acids, esters, hydrozides, anilines, and amines.

[0089] In some embodiments of the invention, the methods of the invention provide a degree of labeling (DOL) of at least 1.8.

[0090] In some embodiments of the invention, the methods of the invention provide a degree of labeling (DOL) of at least 1.9.

[0091] In some embodiments of the present invention, the methods of the present invention provide a degree of labeling (DOL) of 2.

[0092] In some embodiments of the invention, the methods of the invention provide a drug-to-antibody ratio (DAR) of 2.0.

[0093] In some embodiments of the invention, greater than 90% of the antibodies or Fc fusion proteins produced by the methods of the invention are conjugated to two amine compounds.

[0094] In some embodiments of the invention, greater than 95% of the antibodies or Fc-fusion proteins produced by the methods of the invention are conjugated to two amine-containing payloads.

[0095] In some embodiments of the invention, 100% of the antibodies or Fc-fusion proteins produced by the methods of the invention are conjugated to two amine-containing payloads.

[0096] In some embodiments, conjugation occurs at the Fc domain of the antibody.

[0097] In some embodiments, conjugation occurs at Gln295.

[0098] In some embodiments, the methods of the present invention provide antibodies conjugated to an amine-containing payload, preferably via a linker at Gln295, wherein the payload comprises one or more reagents selected from the group consisting of cytotoxic agents, cytostatic agents, chemotherapeutic agents, toxins, radionuclides, DNA, RNA, siRNA, microRNA, peptide nucleic acids, unnatural amino acids, peptides, enzymes, fluorescent tags, biotin, and first click reaction partners. In some embodiments, the cytotoxic agent comprises any agent that is detrimental to cell growth, viability, or proliferation. The payload may also comprise a chelator or a radionuclide. Exemplary radionuclides include: 225 Ac, 212Bi, 131 I, 211 At, 227 Th and 186 Examples of suitable refrigerants include, but are not limited to, Re.

[0099] In some embodiments, the amine compound is an amine-containing payload comprising one or more of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, and a first click reaction partner.

[0100] In certain embodiments, the amine-containing payload comprises a first Click reaction partner, and preferably, the method further comprises reacting the antibody-payload conjugate with a second Click reaction partner comprising one or more of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, and biotin to obtain a second antibody-payload conjugate.

[0101] In some embodiments, the first Click reaction partner is 3-azido-1-propylamine and the second Click reaction partner is DBCO-val-cit-MMAF or DBCO-MMAF.

[0102] Examples of click chemistry methods suitable for use in accordance with the present invention are described, for example, in International Application No. US2018 / 065913, which is incorporated herein by reference.

[0103] Numbered Embodiments Exemplary numbered embodiments of the present invention are provided below. 1. A method for producing a conjugated antibody or a conjugated Fc fusion protein, comprising reacting a glycosylated antibody or a glycosylated Fc fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. 2. The method of embodiment 1, wherein the glycosylated antibody or glycosylated Fc fusion protein has an intact glycan content. 3. The method of embodiment 1 or 2, wherein the amine compound is an amine-containing payload comprising one or more of a cytotoxic drug, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, an imaging agent, or a first click reaction partner. 4. The method of any one of embodiments 1 to 3, wherein the glycosylated antibody or glycosylated Fc fusion protein has not been treated with an endo- or exo-glycosidase prior to reacting the glycosylated antibody or glycosylated Fc fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. 5. The method of any one of embodiments 1 to 4, wherein the glycosylation site of the glycosylated antibody or glycosylated Fc fusion protein has not been glycan engineered or glycan modified prior to reacting the glycosylated antibody or glycosylated Fc fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. 6. The method of any one of embodiments 1 to 5, wherein the glycosylated antibody or glycosylated Fc fusion protein comprises an N-linked glycan at amino acid Asn297. 7. The method of any one of embodiments 1 to 6, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein under low ionic strength conditions is carried out in a solution containing a salt concentration of about 25 mM or less. 8. The method of any one of embodiments 1 to 6, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein under low ionic strength conditions is carried out in a solution containing a salt concentration of about 20 mM or less. 9. The method of any one of embodiments 1 to 6, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein under low ionic strength conditions is carried out in a solution containing a salt concentration of about 15 mM or less. 10. The method of any one of embodiments 1 to 6, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein under low ionic strength conditions is carried out in a solution containing a salt concentration of about 10 mM or less. 11. The method of any one of embodiments 7 to 10, wherein the low ionic strength solution comprises sodium phosphate, potassium phosphate, HEPES, sodium acetate, or Tris. 12. The method of embodiment 11, wherein the low ionic strength solution comprises potassium phosphate. 13. The method of embodiment 11, wherein the low ionic strength solution comprises sodium phosphate. 14. The method of embodiment 11, wherein the low ionic strength solution comprises HEPES. 15. The method of embodiment 11, wherein the low ionic strength solution comprises Tris. 16. The method of embodiment 11, wherein the low ionic strength solution comprises sodium acetate. 17. The method of any one of embodiments 1 to 16, wherein the method for producing a conjugated antibody or conjugated Fc-fusion protein further comprises reducing the ionic strength of the solution containing the glycosylated antibody or glycosylated Fc-fusion protein to provide low ionic strength conditions. 18. The method of any one of embodiments 1 to 17, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein further comprises reducing the ionic strength of the solution containing transglutaminase to provide low ionic strength conditions. 19. The method of embodiment 17 or 18, wherein the ionic strength is reduced by dilution or by buffer exchange by dialysis, diafiltration, filtration, precipitation, and / or chromatographic methods. 20. The method of any one of embodiments 1 to 19, wherein the transglutaminase is a microbial transglutaminase. 21. The method of any one of embodiments 1 to 20, wherein the amine compound is a primary amine compound. 22. The method of embodiment 21, wherein the primary amine compound comprises an azide. 23. The method of any one of embodiments 1 to 22, wherein the method for producing a conjugated antibody or conjugated Fc fusion protein further comprises reacting the conjugated antibody with a reactive payload compound to form an antibody-payload conjugate. 24. The method of any one of embodiments 1 to 23, wherein the method for producing the conjugated antibody or conjugated Fc-fusion protein provides an average degree of labeling (DOL) per heavy chain of at least 0.9. 25. The method of embodiment 24, wherein the method for producing the conjugated antibody or conjugated Fc-fusion protein provides an average degree of labeling (DOL) of 1 per heavy chain. 26. The method of any one of embodiments 1 to 23, wherein the method for producing the conjugated antibody or conjugated Fc-fusion protein provides a DOL of at least 1.8 per antibody. 27. The method of embodiment 26, wherein the method for producing the conjugated antibody or conjugated Fc-fusion protein provides a DOL of 2.0 per antibody. 28. The method of any one of embodiments 1 to 23, wherein 80% or more of the glycosylated antibody or glycosylated Fc fusion protein is converted to a conjugated antibody or conjugated Fc fusion protein, respectively, having a DOL of 2 (i.e., an antibody species or conjugated Fc fusion protein species having a DOL of 2). 29. The method of any one of embodiments 1 to 23, wherein 90% or more of the glycosylated antibody or glycosylated Fc-fusion protein is converted to a conjugated antibody or conjugated Fc-fusion protein, respectively, in 2 DOL. 30. The method of any one of embodiments 1 to 23, wherein 100% of the glycosylated antibody or glycosylated Fc-fusion protein is converted into a conjugated antibody or conjugated Fc-fusion protein, respectively, in 2 DOL. 31. The method of any one of embodiments 1 to 23, wherein the method for producing the conjugated antibody or conjugated Fc-fusion protein provides less than 10% by-products compared to the conjugated antibody or conjugated Fc-fusion protein, respectively. 32. The method of any one of embodiments 24 to 30, comprising measuring the degree of labeling (DOL) by LC-MS. 33. The method of any one of embodiments 1 to 32, wherein the conjugated antibody or conjugated Fc fusion protein is conjugated at its Fc domain. 34. The method of embodiment 33, wherein the conjugated antibody or conjugated Fc-fusion protein is conjugated at Gln295. 35. The method of any one of embodiments 1 to 32, wherein the conjugated antibody or conjugated Fc-fusion protein is conjugated to an amine-containing payload via a linker at Gln295, and the payload comprises one or more reactive groups selected from the group consisting of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, a chelator, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, an imaging agent, and a first click reaction partner. 36. The method of embodiment 35, wherein the amine-containing payload comprises a first Click reaction partner, and the method further comprises reacting the conjugated antibody or conjugated Fc-fusion protein with a second Click reaction partner comprising one or more of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, an imaging agent, or biotin to obtain a second conjugate. 37. The method of embodiment 36, wherein the first click reaction partner is 3-azido-1-propylamine and the second click reaction partner is DBCO-val-cit-MMAF or DBCO-MMAF. 38. A method according to any one of embodiments 1 to 37 for producing a conjugated antibody, comprising reacting a glycosylated antibody with an amine compound in the presence of transglutaminase under low ionic strength conditions. 39. A method according to any one of embodiments 1 to 37 for producing a conjugated Fc-fusion protein, comprising reacting a glycosylated Fc-fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions. 40. A conjugated antibody produced according to the method of any one of embodiments 1 to 38. 41. A pharmaceutical composition comprising the conjugated antibody described in embodiment 40. 42. A conjugated Fc fusion protein produced according to the method of any one of embodiments 1 to 37 or 39. 43. A pharmaceutical composition comprising the conjugated Fc-fusion protein of embodiment 42.

[0104] The following examples of the present invention are provided to further illustrate certain embodiments. It should be understood that the following examples do not limit the scope of the present invention. [Example]

[0105] The antibodies used in the following examples are commercially available and include trastuzumab (Herceptin®), pertuzumab (Perjeta®), and panitumumab (Victibix®). Trastuzumab and pertuzumab bind to human Her2. Panitumumab binds to human EGFR.

[0106] Example 1: Conjugation of trastuzumab with 3-APA under low ionic strength conditions using microbial transglutaminase (MTG) from Zedira Antibody and transglutaminase preparation Proprietary recombinant microbial transglutaminase (MTG or BTG for bacterial transglutaminase) produced in E. coli was purchased from Zedira (catalog number T001). The lyophilized powder was resuspended in water and buffer-exchanged into a low ionic strength buffer (e.g., 10 mM potassium phosphate buffer, pH 7.2) using a Zeba desalting column (Thermo Fisher). Trastuzumab, a humanized IgG1 antibody, was also buffer-exchanged into a low ionic strength buffer (e.g., 10 mM potassium phosphate) using a Zeba desalting column. The buffer-exchanged trastuzumab and microbial transglutaminase were then diluted with water or an appropriate buffer for the desired reaction conditions to a final concentration of 1 mg / mL for the mAb and 10 U / mg for the enzyme. The antibody and enzyme were incubated in a 20- to 100-fold molar excess over the mAb with 3-azidopropylamine (3-APA) substrate, an azide-containing reagent with suitable reactivity for payload conjugation.

[0107] Conjugation Reactions Reactions were stopped at the indicated time points by the addition of C102, an MTG blocker from Zedira that irreversibly alkylates the active site cysteine ​​of microbial transglutaminase. The final concentration of MTG blocker used was 100 μM. For intact mass analysis, mAbs were deglycosylated with Rapid PNGase F (2% v / v) to reduce sample heterogeneity and facilitate analysis; for mass reduction analysis, dithiothreitol or TCEP was added.

[0108] LC-MS was performed on an Agilent 1260 HPLC system connected to an Agilent G6224 MS-TOF mass spectrometer. LC was performed on an Agilent RP-mAb C4 column (2.1 × 50 mm, 3.5 microns) at a flow rate of 1 mL / min using mobile phases of 0.1% formic acid in water (A) and 0.1% formic acid in acetonitrile (Sigma-Aldrich catalog no. 34688) (B), with a gradient of 20% B (0–2 min), 20–60% B (2–3 min), and 60–80% B (3–5.5 min). The instrument was operated in positive electrospray ionization mode, scanning from m / z 600 to 6000. Instrument settings included capillary voltage 3500 V, fragmentor 175 V, skimmer 65 V; gas temperature 325 °C, drying gas flow rate 5.0 L / min, nebulizer pressure 30 psig, and acquisition mode range 100–7000 with a 0.42 scan rate.

[0109] Mass-to-charge spectra were deconvoluted using a maximum entropy algorithm, and the relative intensities of the deconvoluted masses corresponding to intact mAb or mAb heavy chain spiked with multiples of 83 Da (corresponding to 3-APA) were used to estimate the degree of labeling (DOL) for each reaction.

[0110] Figure 1 shows the kinetics of MTG-catalyzed conjugation of 3-APA to intact and deglycosylated trastuzumab in different reaction buffer compositions. The conjugation rate of deglycosylated mAb in PBS buffer was very fast, with the reaction being complete within 3 h. The conjugation rate of deglycosylated mAb appeared to be even faster in 10 mM phosphate buffer. The conjugation rate of glycan-intact mAb was slower in PBS, reaching only 25% conversion in 5 h, with overnight conversion progress ranging from 40 to 60% (data not shown). However, conjugation of glycan-intact mAb in 5 or 10 mM phosphate buffer was significantly faster than in PBS buffer, reaching approximately 70 to 80% completion after 5 h and reaching complete or nearly complete conversion after longer incubation times (data not shown). Reactions performed under low ionic strength conditions showed improved conjugation rates compared to reactions performed in PBS. Both 10 mM and 5 mM phosphate buffers showed significant rate enhancement compared to PBS (8 mM sodium phosphate, 1.5 mM potassium phosphate, 2.7 mM KCl, 138 mM NaCl).

[0111] Transglutaminase reactions were tested in a panel of different buffer conditions using 1 mg / mL of the human IgG1 antibody trastuzumab, a 100 molar excess (690 μM) of 3-APA, and Zedira transglutaminase (catalog no. T001) at 10 U / mg of antibody. Table 2 shows the fraction of fully modified and glycan-intact WT human trastuzumab after 18-20 hours of incubation (at DOL=2) with MTG and 3-APA at 37°C under a range of reaction conditions. Many low ionic strength formulations showed increased modification, often allowing complete or near-complete modification.

[0112] [Table 2-1]

[0113] [Table 2-2]

[0114] Reactions performed under low ionic strength conditions, including potassium phosphate buffer at pH 5.8, 7.2, or 8.0, HEPES buffer at pH 7.2 or 8.0, Tris buffer at pH 7.2, 8.0, or 9.2, and sodium acetate buffer at pH 5.6, resulted in increased modification of mAbs with 3-APA. In all cases, complete or nearly complete conversion of the mAb to a DOL of 2 was achieved after 16–20 h at 37°C in a 2.2 mM buffer. In many cases, complete conjugation (reactions achieving a DOL of 2) was achieved at 6.2 mM and 11.2 mM, and in these cases, the low-salt conditions produced significantly more conjugate than PBS or other higher ionic strength reaction conditions. Under low pH conditions (pH 3.6 and 4.2), limited product was produced in most conditions tested in sodium acetate buffer, likely due to suboptimal pH conditions for MTG. One exception is the reaction with 2.2 mM sodium acetate, pH 4.2, which resulted in complete modification of the mAb with 3-APA, which may be explained by limited buffer capacity inability to maintain a low pH.

[0115] Peptide mapping Peptide mapping experiments were performed on the resulting conjugate to identify the conjugation site. 50 μg of mAb in 50 μL of PBS was mixed with 150 μL of 8 M GuHCl, 4 mM EDTA, and 30 mM DTT at pH 8.0 and incubated at 37°C for 1 hour. Cysteines were alkylated by adding 24 μL of 0.5 M iodoacetamide (IAA) and incubating the reaction mixture in the dark at room temperature for 1 hour. The mAb was then exchanged into 50 mM Tris, 1 mM CaCl2, pH 8.0 using a Zeba spin column (Thermo) and then divided into 90 μL for trypsin digestion and 130 μL for chymotrypsin digestion. Fifteen microliters of 0.1 mg / mL trypsin / Lys-C (Promega #V507) or 0.1 mg / mL chymotrypsin in 1 mM HCl was added, and the samples were incubated at 37°C for 4 hours for trypsin / Lys-C digestion or at room temperature in the dark for 4 hours for chymotrypsin digestion. LC-MS / MS data were acquired on a SCIEX Triple TOF 6600. Data were processed using Protein Metrics software, Byos (version 3.5-10x64). Peptide mapping experiments demonstrated that the modification was localized to Gln295 (Figures 2A-2D).

[0116] Biophysical characterization of the conjugates Melting and Coagulation Temperatures Biophysical characterization of conjugated trastuzumab was performed to determine the effect of conjugation on antibody stability. Data were compared to unconjugated wild-type (WT) trastuzumab. The unfolding temperature (T) was measured in PBS by differential scanning fluorescence using a Prometheus nanoDSF instrument from Nanotemper. m ) (Figure 3A) and agglomeration temperature (T agg ) (Figure 3B). Tm was determined by monitoring the change in fluorescence intensity at 330 nm and 350 nm during a thermal scan from 20°C to 95°C, and Tagg was determined by monitoring scattering. The T of the trastuzumab azide conjugatem was determined to be 68.3°C for the first transition (corresponding to the CH2 domain), a difference of 2.1°C relative to the glycosylated wild-type mAb. The second transition (corresponding to the Fab) was determined to be 79.2°C, a difference of 0.3°C relative to the glycosylated wild-type mAb. In contrast, deglycosylation of trastuzumab reduced the Tm of the CH2 domain by approximately 8°C. The aggregation temperatures (Tagg) of the glycosylated and deglycosylated trastuzumab conjugates were similar, with Tag at 77.7°C, but 1.1°C lower when compared to glycosylated unconjugated trastuzumab (Table 3).

[0117] [Table 3]

[0118] Analytical Size Exclusion Chromatography (SEC) The oligomerization state of the conjugated mAb was measured by analytical size-exclusion chromatography for both the azide-modified mAb and the conjugated mAb in which the drug payload DBCO-val-cit-MMAF was attached to the azide-modified mAb. In both cases, the elution profile was essentially identical to that of unconjugated trastuzumab and consistent with 100% monomer.

[0119] Conjugate activity To demonstrate that the activity of conjugates generated under low ionic strength conditions for glycosylated mAbs is comparable to that of conjugates generated by established methods, we conjugated azido-mAbs generated under low-salt conditions to drug payloads and demonstrated their activity in cellular assays (Figure 4). Trastuzumab was either conjugated to 3-APA under low-salt conditions as described above or deglycosylated overnight at 37°C using 1 U / mL Rapid PNGase F (New England Biolabs) and then reacted with 3-APA (100-fold molar excess) and MTG (Activa TI, 5–20% w / v or Zedira, 5–20 units / mg mAb) in PBS buffer at 37°C for 2–4 hours. The DBCO-Val-Cit-PABC-MMAF drug payload was added to the azide-conjugated mAb in a 10-fold molar excess and reacted via strain-promoted click chemistry (SPAAC) at room temperature for 2–6 h. Free drug was removed from the resulting ADC using a Zeba desalting column (Thermo).

[0120] SKBR3 cells, a Her2-high cell line, were treated with various concentrations of ADC for 72 hours at 37°C. Cell viability at the end of treatment was measured using Cell Titer Glo. The cytotoxic activity of trastuzumab-vcMMAF produced by the conventional conjugation method, including a deglycosylation step, was found to be similar to that of trastuzumab-vcMMAF produced under low ionic strength conditions using a glycosylated antibody (Figure 4).

[0121] Example 2: Conjugation of trastuzumab with 3-APA under low ionic strength conditions using Activa TI microbial transglutaminase A low ionic strength conjugation method was also successfully demonstrated using Activa TI MTG enzyme purchased from Ajinomoto.

[0122] Conjugation of trastuzumab under low ionic strength conditions using buffer-exchanged Activa TI microbial transglutaminase. Activa TI MTG is typically formulated with maltodextrin, a polysaccharide used as a food additive and for other applications. Initial conjugation experiments were performed with resolubilized Activa TI MTG. Trastuzumab was exchanged into 10 mM potassium phosphate buffer, pH 7.2, using a Zeba desalting column (Thermo). Activa TI powder was dissolved in 10 mM potassium phosphate buffer, and 3-APA was dissolved in water. The reaction components were combined in a reaction mixture with a final concentration of 1 mg / mL trastuzumab, 690 μM 3-APA, and 20% w / v Activa TI MTG in 10 mM potassium phosphate, pH 7.2. For comparison, identical reactions were set up in PBS buffer (1 mg / mL trastuzumab, 690 μM 3-APA, 20% w / v Activa TI MTG, 1.5 mM KH2PO4, 8.1 mM Na2HPO4, 2.7 mM KCl, 137 mM NaCl pH 7). The reactions were incubated overnight at 37°C. For analysis, MTG was inactivated by the addition of an MTG blocker, and the mAb was deglycosylated with Rapid PNGase F (1% v / v) for 20 min at 50°C and reduced to 50 mM with DTT, followed by LC-MS to measure the DOL.

[0123] The data showed that the DOL remained low in the presence of maltodextrin and altering the buffer composition did not increase the conjugation rate (Table 4). Conjugation of trastuzumab under low ionic strength conditions using purified Activa TI microbial transglutaminase. To remove maltodextrin from commercially available MTG, MTG obtained from Ajinomoto was purified from the Activa TI formulation by cation exchange chromatography (CEX) and further exchanged into a low-salt buffer. 50 mg of Activa transglutaminase powder was dissolved in 500 mL of 20 mM sodium acetate pH 5.2. The sample was purified using a 5 mL SP HP HiTrap column (GE) mounted on an Akta Avant at room temperature at a flow rate of 5 mL / min. The method involved a 5 column volume (CV) equilibration, a 5 CV wash, followed by a 0-55% gradient of buffer B over 20 CV (Buffer A = 20 mM sodium acetate pH 5.2; Buffer B = 20 mM sodium acetate pH 5.2, 1 M NaCl). Fractions containing MTG were pooled and concentrated using an Amicon concentrator (MWCO = 10 kDa). The concentrated enzyme was then exchanged into 10 mM phosphate buffer pH 7.2 on a Zeba desalting column.

[0124] Trastuzumab was incubated overnight at 37°C with transglutaminase and 3-APA at concentrations of 1 mg / ml antibody, 69 μM transglutaminase, and 690 μM 3-APA in 10 mM phosphate buffer, pH 7.2. With this purified MTG, production of purified mAb with a DOL of 2 was increased 4-fold under low-salt conditions compared to standard conditions (Table 4).

[0125] [Table 4]

[0126] Example 3: Conjugation of PSMA monoclonal antibodies PSMB127, a human IgG4 mAb that binds to prostate-specific membrane antigen (PSMA), was conjugated with MTG under low ionic strength conditions. Using a Zeba desalting column (Thermo), PSMB127 was exchanged into 10 mM potassium phosphate buffer, pH 7.2. Zedira MTG was exchanged into 10 mM potassium phosphate buffer, and 3-APA was dissolved in water. The components were combined in a reaction mixture with final concentrations of 1 mg / mL PSMB127, 690 μM 3-APA, and 10 U / mg Zedira MTG in 0.9 mM potassium phosphate, pH 7.2. For comparison, identical reactions were set up in a PBS-based buffer (1 mg / mL PSMB127, 690 μM 3-APA, 10 U / mg Zedira MTG in 1.5 mM KH2PO4, 8.1 mM Na2HPO4, 2.7 mM KCl, 167 mM NaCl, 5 mM sodium acetate pH 7). Reactions were incubated overnight at 37°C. For analysis, MTG was inactivated by the addition of an MTG blocker, and the mAb was deglycosylated with Rapid PNGase F (1% v / v) at 50°C for 20 min and reduced to 50 mM with DTT or 5 mM with TCEP, followed by LC-MS to measure DOL.

[0127] [Table 5]

[0128] Example 4: Conjugation of Pertuzumab with 3-APA under low ionic strength conditions Pertuzumab, a human IgG1 mAb that binds to Her2, was conjugated with MTG under low ionic strength conditions. Clinical-grade pertuzumab was obtained from Genentech and exchanged into 10 mM potassium phosphate buffer, pH 7.2, using a Zeba desalting column (Thermo). Zedira MTG was exchanged into 10 mM potassium phosphate buffer, and 3-APA was dissolved in water. The components were combined in a reaction mixture with final concentrations of 1 mg / mL pertuzumab, 690 μM 3-APA, and 10 U / mg Zedira MTG in 0.9 mM potassium phosphate, pH 7.2. For comparison, identical reactions were set up in a PBS-based buffer containing additional buffer components from the mAb and enzyme preparations (1.5 mM KH2PO4, 7.8 mM Na2HPO4, 2.6 mM nKCl, 163 mM NaCl, 5 mM sodium acetate, 0.6 mM histidine acetate, 3.9 mM sucrose, 1 mg / mL pertuzumab in 0.001% polysorbate 20 pH 7, 690 μM 3-APA, and 10 U / mg Zedira MTG). Reactions were incubated overnight at 37 °C. For analysis, MTG was inactivated by the addition of an MTG blocker, and the mAb was deglycosylated with Rapid PNGase F (1% v / v) at 50 °C for 20 min and reduced to 50 mM with DTT or 5 mM with TCEP, followed by LC-MS to measure DOL.

[0129] [Table 6]

[0130] Example 5: Conjugation of panitumumab with 3-APA under low ionic strength conditions Panitumumab, a human IgG2 mAb that binds to EGFR, was conjugated with MTG under low ionic strength conditions. Clinical-grade panitumumab was obtained from GSK and exchanged into 10 mM potassium phosphate buffer, pH 7.2, using a Zeba desalting column (Thermo). Zedira MTG was exchanged into 10 mM potassium phosphate buffer, and 3-APA was dissolved in water. The components were combined in a reaction mixture to a final concentration of 1 mg / mL panitumumab, 690 μM 3-APA, and 10 U / mg Zedira MTG in 0.9 mM potassium phosphate, pH 7.2. For comparison, identical reactions were set up in a PBS-based buffer containing additional buffer components from the mAb and enzyme preparations (1 mg / mL panitumumab, 690 μM 3-APA, and 10 U / mg Zedira MTG in 1.4 mM KH2PO4, 7.7 mM Na2HPO4, 2.6 mM KCl, 165 mM NaCl, 8.6 mM sodium acetate, pH 7). Reactions were incubated overnight at 37°C. For analysis, MTG was inactivated by the addition of an MTG blocker, and the mAb was deglycosylated with Rapid PNGase F (1% v / v) at 50°C for 20 min and reduced to 50 mM with DTT or 5 mM with TCEP, followed by LC-MS to measure DOL.

[0131] Reactions performed in 10 mM potassium phosphate showed 69% conjugation, while in reactions performed in PBS, only 28% of panitumumab achieved a DOL of 2 (Table 7).

[0132] [Table 7]

[0133] Example 6: Conjugation of trastuzumab to a series of substrates under low ionic strength conditions A series of amine-containing substrates was obtained for conjugation with MTG under low salt conditions. Three additional azide-containing amines of various sizes were tested, with the linker length between the amine and azide ranging from 11 to 71 atoms. The biotin-conjugated amine pentylaminobiotin was also tested, as was an amine attached to the cytotoxic payload MMAF. The substrates tested are shown in Table 8:

[0134] [Table 8]

[0135] To evaluate conjugation efficiency under low ionic strength conditions, trastuzumab and Zedira MTG were exchanged into 5 mM potassium phosphate buffer, pH 7.2, using a Zeba desalting column. The components were combined in a reaction mixture with final concentrations of 1 mg / mL trastuzumab, 690 μM substrate, and 10 U / mg Zedira MTG in 5 mM potassium phosphate, pH 7.2. For comparison, identical reactions were set up in a PBS-based buffer containing additional buffer components from the mAb and enzyme preparations (1 mg / mL trastuzumab, 690 μM substrate, and 10 U / mg Zedira MTG in 1.4 mM KH2PO4, 7.7 mM Na2HPO4, 2.6 mM KCl, 165 mM NaCl, 8.6 mM sodium acetate, pH 7). The reaction was incubated at 37°C for 18 hours. For analysis, MTG was inactivated by the addition of an MTG blocker, and the mAb was deglycosylated with Rapid PNGase F (1% v / v) for 20 min at 50°C and reduced to 20 mM with DTT, followed by LC-MS to measure the DOL.

[0136] Reactions performed in 5 mM potassium phosphate showed increased conjugation compared to PBS reactions (Table 9). A series of azide-containing amines all showed increased conversion of mAb to DOL=2 species under low salt conditions. In general, larger substrates produced less product than smaller substrates in both PBS and 5 mM phosphate. The pentylaminobiotin substrate was 98% conjugated to DOL=2 under low salt conditions, but only 40% in PBS. The amine-vcMMAF molecule was 50% converted to DOL=2 under these conditions in 5 mM phosphate, but only 4% in PBS.

[0137] [Table 9]

[0138] Various human IgG antibodies of various isotypes and properties described above showed enhanced conjugation rates under low ionic strength conditions. These included the human IgG4 mAb PSMB127 (Example 3), the human IgG1 mAbs trastuzumab and pertuzumab (Examples 1, 2, and 4), and the human IgG2 mAb panitumumab (Example 5). Most showed >90% conjugation to a DOL of 2 under the low ionic strength conditions of the present invention. In summary, using various amine substrates, reaction conditions have been identified that allow the conjugation of wild-type human IgG to full modification at Gln295 (DOL=2) in an MTG-catalyzed reaction. Glycan engineering was not required; the glycans remained intact, preserving the biophysical and immunological properties of the mAb.

[0139] These results demonstrate that the use of low ionic strength buffer conditions provides consistent and reproducible labeling of glycan-intact antibodies. Under low ionic strength conditions (e.g., about 15 mM or less salt buffer, or about 12 mM or less salt buffer, or about 10 mM or less salt buffer, or about 10 mM salt buffer), over 90% of antibodies consistently exhibit a DOL of 2, regardless of the nature of the antibody or drug conjugate.

[0140] Table 10

Claims

1. 1. A method for producing a conjugated antibody or a conjugated Fc-fusion protein, comprising reacting a glycosylated antibody or a glycosylated Fc-fusion protein with an amine compound in the presence of transglutaminase under low ionic strength conditions; The low ionic strength conditions are buffer conditions in which the salt concentration of the buffer is or is maintained at a concentration of less than about 30 mM; The low ionic strength conditions are applied before the reaction is carried out, the glycosylated antibody comprises a heavy chain selected from the group consisting of IgA1, IgA2, IgD, IgE, IgG1, IgG2, IgG3, IgG4, and IgM heavy chains; the glycosylated Fc-fusion protein comprises at least one Fc polypeptide linked to a protein or peptide by a C-terminal fusion or an N-terminal fusion, the Fc polypeptide of the Fc-fusion protein comprising an IgG CH2 and an IgG CH3 constant domain sequence; the glycosylated antibody or the glycosylated Fc fusion protein has an intact glycan content containing an N-linked glycan at amino acid Asn297 according to the EU index as set forth in Kabat; the conjugated antibody or the conjugated Fc-fusion protein is conjugated at its Fc domain; the amine compound comprises a substrate selected from the group consisting of 3-azidopropylamine, azido-PEG3-amine, azido-dPEG11-amine, azido-dPEG23-amine, pentylaminobiotin, and amino-PEG4-Val-Cit-PABC-MMAF; and The low ionic strength conditions include pH 7.2 in about 5 mM or about 10 mM phosphate buffer, in about 2 mM to about 12 mM potassium phosphate buffer at pH 5.8, 7.2, or 8.0; about 2 mM to about 12 mM HEPES at pH 7.2 or 8.0; in about 2 mM to about 12 mM Tris at pH 7.2, 8.0, or 9.2; pH 5.6 in about 2 mM to about 12 mM sodium acetate, and in about 2 mM to about 3 mM sodium acetate at pH 4.

2.

2. The method of claim 1, wherein the glycosylated antibody or the glycosylated Fc-fusion protein has not been treated with an endo- or exo-glycosidase prior to reacting the glycosylated antibody or the glycosylated Fc-fusion protein with the amine compound in the presence of the transglutaminase under the low ionic strength condition.

3. 3. The method of claim 1 or 2, wherein the glycosylation site of the glycosylated antibody or the glycosylated Fc-fusion protein has not been glycan engineered or glycan modified prior to reacting the glycosylated antibody or the glycosylated Fc-fusion protein with the amine compound in the presence of the transglutaminase under the low ionic strength conditions.

4. 4. The method of any one of claims 1 to 3, wherein the method of producing the conjugated antibody or the conjugated Fc-fusion protein further comprises reducing the ionic strength of a solution containing the glycosylated antibody or the glycosylated Fc-fusion protein to provide the low ionic strength conditions.

5. 5. The method of any one of claims 1 to 4, wherein the method for producing the conjugated antibody or the conjugated Fc-fusion protein further comprises reducing the ionic strength of a solution containing the transglutaminase to provide the low ionic strength conditions.

6. 6. The method of claim 4 or 5, wherein the ionic strength is reduced by dilution, dialysis, diafiltration, filtration, precipitation, and / or buffer exchange by chromatographic methods.

7. The method according to any one of claims 1 to 6, wherein the transglutaminase is a microbial transglutaminase.

8. 8. The method of any one of claims 1 to 7, wherein the method of producing the conjugated antibody or the conjugated Fc-fusion protein further comprises reacting the conjugated antibody with a reactive payload compound to form an antibody-payload conjugate.

9. The method for producing the conjugated antibody or the conjugated Fc-fusion protein comprises: (E) providing an average degree of labeling (DOL) of at least 0.9 per heavy chain; (F) providing at least 1 DOL per heavy chain; (G) providing a DOL of at least 1.8 per antibody; or (K) The method of any one of claims 1 to 8, providing a DOL of at least 2.0 per antibody.

10. of the glycosylated antibody or the glycosylated Fc fusion protein (L) 80% or more (M) 90% or more, or 9. The method of any one of claims 1 to 8, wherein (N) 100% is converted to the conjugated antibody or conjugated Fc-fusion protein, respectively, having a DOL of 2 (i.e., an antibody species or conjugated Fc-fusion protein species having a DOL of 2).

11. 9. The method of any one of claims 1 to 8, wherein the method of producing the conjugated antibody or the conjugated Fc-fusion protein provides less than 10% by-products compared to the conjugated antibody or the conjugated Fc-fusion protein, respectively.

12. The method of any one of claims 9 to 11, comprising measuring the degree of labeling (DOL) by LC-MS.

13. The method of any one of claims 1 to 12, wherein the conjugated antibody or the conjugated Fc-fusion protein is conjugated at its Fc domain.

14. 14. The method of claim 13, wherein the conjugated antibody or the conjugated Fc-fusion protein is conjugated at Gln295 according to the EU index as set forth in Kabat.

15. 13. The method of any one of claims 1 to 12, wherein the conjugated antibody or the conjugated Fc-fusion protein is conjugated to an amine-containing payload via a linker at Gln295, wherein the payload comprises one or more reactive groups selected from the group consisting of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, a chelator, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, biotin, an imaging agent, and a first click reaction partner.

16. 16. The method of claim 15, wherein the amine-containing payload comprises the first Click reaction partner, the method further comprising reacting the conjugated antibody or the conjugated Fc-fusion protein with a second Click reaction partner comprising one or more of a cytotoxic agent, a cytostatic agent, a chemotherapeutic agent, a toxin, a radionuclide, DNA, RNA, siRNA, microRNA, peptide nucleic acid, an unnatural amino acid, a peptide, an enzyme, a fluorescent tag, an imaging agent, or biotin to obtain a second conjugate.

17. 17. The method of claim 16, wherein the first click reaction partner is 3-azido-1-propylamine and the second click reaction partner is DBCO-val-cit-MMAF or DBCO-MMAF.

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