Modified polyamine polymers for delivery of biomolecules into cells - Patents.com

Abstract

Provided herein are compounds, compositions, and methods for delivering biomolecules to cells. In particular, the present disclosure provides modified polyamine polymers, including polyamine polymers having fluorinated substituents.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims priority to U.S. Provisional Patent Application No. 62 / 865,638, filed June 24, 2019, the entire contents of which are fully incorporated by reference herein.

[0002] INCORPORATION BY REFERENCE OF MATERIAL SUBMITTED ELECTRONICALLY The computer readable nucleotide / amino acid sequence listing, filed contemporaneously herewith and identified below as a single ASCII (text) file of 10,000 bytes, entitled "36754-601_ST25" created on June 23, 2020, is hereby incorporated by reference in its entirety.

[0003] Provided herein are compounds, compositions, and methods for delivering biomolecules to cells. In particular, the present disclosure provides modified polyamine polymers, including polyamine polymers having fluorinated substituents. [Background technology]

[0004] Cationic polymers such as polyethylenimine (PEI) and poly(amidoamine) (PAMAM) dendrimers are widely used as carriers for introducing foreign genes into cells. These materials are easy to manufacture and have excellent safety compared with viral gene delivery. However, their commercial and clinical applications are limited by relatively low transfection efficiency and poor cell viability. Summary of the Invention

[0005] Provided herein are compounds, compositions, and methods for delivering biomolecules to cells. In particular, the present disclosure provides modified polyamine polymers, including polyamine polymers having fluorinated substituents.

[0006] An embodiment of the disclosure is a compound or a salt thereof, the compound comprising: A polyethyleneimine polymer; and a plurality of substituents attached to amino groups of the polyethyleneimine polymer, each substituent independently having the formula (I): -X-(CH2) n -Z (I), During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, 2, 3, 4, or 5; The present invention includes compounds or salts thereof, wherein Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group.

[0007] In some embodiments, the polyethyleneimine polymer has a weight average molecular weight of about 500 Da to about 250,000 Da. In some embodiments, the polyethyleneimine polymer has a weight average molecular weight of about 500 Da to about 2,000 Da. In some embodiments, the polyethyleneimine polymer has a weight average molecular weight of about 5,000 Da to about 25,000 Da.

[0008] In some embodiments, the polyethyleneimine polymer is a branched polyethyleneimine polymer. In some embodiments, the polyethyleneimine polymer is a linear polyethyleneimine polymer.

[0009] In some embodiments, Z has the formula: -(CF2) m In some embodiments, Z is a haloalkyl group having -CF3, where m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, Z is a pentafluorophenyl group. In some embodiments, Z is an unsubstituted pyridyl group.

[0010] In some embodiments, X is —C(O)O— and n is 1 or 2.

[0011] In some embodiments, Z has the formula: -(CF2) m—CF3, where m is 1, 2, 3, 4, or 5.

[0012] In some embodiments, X is a bond and n is 1 or 2.

[0013] In some embodiments, about 0.1 mol % to about 60 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I). In some embodiments, about 5 mol % to about 50 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I). In some embodiments, about 8 mol % to about 40 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I).

[0014] An embodiment of the present disclosure is also a compound or a salt thereof, the compound comprising: a poly(amidoamine) dendrimer; and a plurality of substituents attached to amino groups of the poly(amidoamine) dendrimer, each substituent independently having the formula (I): -X-(CH2) n -Z (I), During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, or 2; The present invention includes compounds or salts thereof, wherein Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group.

[0015] In some embodiments, the poly(amidoamine) dendrimer is a first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, or tenth generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a first, second, third, or fourth generation poly(amidoamine) dendrimer.

[0016] In some embodiments, Z has the formula: -(CF2) mIn some embodiments, Z is a haloalkyl group having -CF3, where m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. In some embodiments, Z is a pentafluorophenyl group. In some embodiments, Z is an unsubstituted pyridyl group.

[0017] In some embodiments, X is -C(O)O-. In some embodiments, Z is of the following formula: -(CF2) m —CF3, where m is 1, 2, 3, 4, or 5.

[0018] In some embodiments, X is a bond and n is 1.

[0019] In some embodiments, about 0.1 mol % to about 80 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I). In some embodiments, about 10 mol % to about 70 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I). In some embodiments, about 20 mol % to about 70 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I).

[0020] Embodiments of the present disclosure also include a method of delivering a biomolecule to a cell, comprising contacting the cell with an effective amount of a compound described herein (i.e., a compound comprising a polyethyleneimine polymer and a plurality of substituents of formula (I), or a compound comprising a poly(amidoamine) dendrimer and a plurality of substituents of formula (I)), or a salt thereof, and contacting the cell with the biomolecule. In some embodiments, the method comprises contacting the cell with an effective amount of two or more different compounds or salts thereof.

[0021] In some embodiments, the biomolecule is at least one of a deoxyribonucleic acid (DNA) molecule, a ribonucleic acid (RNA) molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof. In some embodiments, the biomolecule is a deoxyribonucleic acid (DNA) molecule or a ribonucleic acid (RNA) molecule. In some embodiments, the biomolecule is a peptide or polypeptide capable of luminescence activity. In some embodiments, the biomolecule comprises a polypeptide sequence of SEQ ID NO: 4 (LgBiT). In some embodiments, the biomolecule is a ribonucleoprotein complex comprising a Cas9 protein. In some embodiments, the ribonucleoprotein complex further comprises a guide RNA (gRNA) and a donor DNA template, the donor DNA template comprising a sequence encoding a polypeptide from SEQ ID NO: 3.

[0022] In some embodiments, the method comprises mixing the compound and the biomolecule to form a mixture, and then contacting a cell with the mixture.

[0023] Embodiments of the present disclosure also include a kit comprising a compound or a salt thereof, wherein the compound or salt thereof is a compound described herein (i.e., a compound comprising a polyethyleneimine polymer and a plurality of substituents of formula (I), or a compound comprising a poly(amidoamine) dendrimer and a plurality of substituents of formula (I)).

[0024] In some embodiments, the kit comprises the compound or the salt thereof in a container.

[0025] In some embodiments, the kit further comprises at least one of a DNA molecule, an RNA molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof. In some embodiments, the biomolecule is a peptide or polypeptide capable of luminescence activity. In some embodiments, the biomolecule comprises a polypeptide sequence of SEQ ID NO: 4 (LgBiT). In some embodiments, the peptide comprises a Cas9 protein. In some embodiments, the DNA molecule is a donor DNA template comprising a sequence encoding a polypeptide from SEQ ID NO: 3.

[0026] In some embodiments, the kit further comprises instructions for using the compound or the salt thereof for transfection of a biomolecule.

[0027] Embodiments of the present disclosure also include a method of modifying the sequence of an endogenous protein in a cell, the method comprising: Assembling a ribonucleoprotein (RNP) complex containing the Cas9 protein, a donor DNA template, and a guide RNA; and delivering the RNP complex into the cell using a compound described herein.

[0028]

[0013] Embodiments of the present disclosure also include a method for tagging an endogenous protein in a cell, the method comprising: assembling a ribonucleoprotein (RNP) complex comprising a Cas9 protein, a donor DNA template, and a guide RNA, the donor DNA template comprising a sequence encoding a peptide or polypeptide tag sequence; and delivering the RNP complex into the cell using a compound described herein.

[0029] In some embodiments, the donor DNA template comprises a sequence encoding a peptide tag selected from SEQ ID NO: 3 and SEQ ID NO: 5. In some embodiments, the donor DNA template further comprises homology arms flanking the sequence encoding the peptide or polypeptide tag sequence. [Brief description of the drawings]

[0030] [Figure 1] AB illustrate results from transfection of HEK293 cells with fixed molar ratios of modified PEI polymers as described in Example 2. A shows transfection efficiency of NanoLuc® vectors as measured by NanoLuc® expression levels. B shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay. [Diagram 2] AB illustrate results from transfection of HEK293 cells with modified PEI compounds as described in Example 2, compared to unmodified polymer and FuGENE HD as controls. A shows the ratio of luminescent signal from NanoLuc compared to the control. B shows measurements of cell viability using the CellTiter-Glo® Luminescent Cell Viability Assay, compared to samples without transfection reagent. [Figure 3A] FIG. 1 illustrates results from transfection of HEK cells following titration of modified PEI polymers and incubation with a fixed amount of DNA, as described in Example 2. Data from transfections performed in the presence of serum are shown. [Figure 3B] FIG. 1 illustrates results from transfection of HEK cells following titration of modified PEI polymers and incubation with a fixed amount of DNA, as described in Example 2. Data from transfections performed in the absence of serum are shown. [Figure 3C] 1 illustrates the results from transfection of HEK cells following titration of modified PEI polymers and incubation with a fixed amount of DNA as described in Example 2. Measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay after transfection in the presence of serum are shown. [Figure 4A]FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4B] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4C] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4D] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4E] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4F] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4G]FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4H] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 4I] FIG. 1 illustrates luminescence results using Nano-Glo® reagent from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of nine different cell types in the presence of serum. [Figure 5A] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5B] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5C] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5D] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5E] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5F] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5G] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 5H] 1 shows measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in nine different cell types in the presence of serum, as described in Example 2. [Figure 6] A-E illustrate the results from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of five different cell types in the presence of serum. [Figure 7] A-D show measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in four different cell types in the presence of serum, as described in Example 2. [Figure 8] A-E illustrate the results from titration of modified PEI and PAMAM polymers and incubation with a fixed amount of DNA as described in Example 2, followed by transfection of five different cell types in the presence of serum. [Figure 9] A-D show measurements of cell viability using the CellTiter-Glo® luminescent cell viability assay following transfection with modified PEI and PAMAM polymers in five different cell types in the presence of serum, as described in Example 2. [Figure 10] A-B illustrate the results of delivering LgBiT to clones that stably expressed HiBiT fusions. A illustrates the results of delivering LgBiT to PKCα-HiBiT or HDAC6-HiBiT clones in HeLa cells or CDK6-HiBiT clones in HEK293 cells using modified PEI compounds, compared to unmodified polymers and linear transduction of BacMam CMV-LgBiT into the corresponding clones above. For the various PEI compounds tested, the percentage of luminescence signal from PKCα-HiBiT, HDAC6-HiBiT, or CDK6-HiBiT clones delivered with LgBiT is shown relative to the luminescence signal from the corresponding BacMam CMV-LgBiT-transduced HiBiT clone. B illustrates the results of delivering LgBiT to HDAC2-HiBiT clones of HeLa cells or CDK12-HiBiT clones of HEK293 cells using modified PEI compounds compared to unmodified polymers and linear transduction of BacMam CMV-LgBiT to the corresponding clones above. For the various PEI compounds tested, the percentage of luminescence signal from HDAC2-HiBiT clones of HeLa cells or CDK12-HiBiT clones of HEK293 cells delivered with LgBiT is shown compared to the corresponding BacMam CMV-LgBiT-transduced HiBiT-clone. [Figure 11]A-B illustrate cell viability measurements of HiBiT clones derived from HeLa and HEK293 cells after delivery of LgBiT. A contains PKCα-HiBiT, HDAC6-HiBiT, and CDK6-HiBiT. B contains HDAC2-HiBiT and CDK12-HiBiT. LgBiT delivery to these cells was by either modified PEI compounds or unmodified polymers. The negative control was no PEI addition to the cells. Luminescent signal (RLU) represents cell viability as measured using the CellTiter-Glo® Luminescent Cell Viability Assay. [Figure 12A] 13 illustrates the results of bioluminescence imaging in which LgBiT was delivered by modified PEI compound 7666-3 to clones that stably expressed HDAC2-HiBiT in HeLa cells or HDAC6-HiBiT in HeLa cells. [Figure 12B] FIG. 13 illustrates bioluminescence imaging results of LgBiT delivered by modified PEI compound 7668-1 to clones that stably expressed HDAC2-HiBiT in HeLa cells or HDAC6-HiBiT in HeLa cells. [Figure 12C] FIG. 13 illustrates bioluminescence imaging results of LgBiT delivered by modified PEI compound 7669-2 to clones that stably expressed HDAC2-HiBiT in HeLa cells or HDAC6-HiBiT in HeLa cells. [Figure 13] AB illustrate the results of screening modified PEI compounds and unmodified PEI to test delivery of LgBiT to different HiBiT-edited cells. A illustrates the percentage of LgBiT delivery by PEI compared to BacMam-LgBiT transduction. B represents the viability of cells treated with PEI-LgBiT complexes for 24 hours. [Figure 14A] Illustrated are the results of bioluminescence imaging of different cell lines after delivery of LgBiT to HiBiT-tagged proteins localized on the cell surface, cytoplasm, and nucleus. [Figure 14B]Illustrated are the results of bioluminescence imaging of different cell lines after delivery of LgBiT to HiBiT-tagged proteins localized on the cell surface, cytoplasm, and nucleus. [Figure 14C] Illustrated are the results of bioluminescence imaging of different cell lines after delivery of LgBiT to HiBiT-tagged proteins localized on the cell surface, cytoplasm, and nucleus. [Figure 15A] Fluorescence imaging of HeLa cells following HaloTag-LgBiT delivery using modified PEI compared to unmodified PEI is shown. [Figure 15B] Fluorescence imaging of HeLa cells following HaloTag-LgBiT delivery using modified PEI compared to unmodified PEI is shown. [Figure 15C] Fluorescence imaging of HeLa cells following HaloTag-LgBiT delivery using modified PEI compared to unmodified PEI is shown. [Figure 16] A-B illustrate results from RNP delivery of the VS-HiBiT tag on the C-terminus of GAPDH in HEK293 cells using modified PEI compound 7667-4 compared to FuGENE HD, ViaFect™, CRISPRMax, and nucleofection as controls. Luminescence signal (RLU) normalized to cell number represents the efficiency of RNP delivery. Cell number is determined by CellTiter-Glo® luminescent cell viability assay (A). Increasing the concentration of PEI shows improved RNP delivery but causes higher cytotoxicity (B). [Figure 17A]Illustrates the delivery of a constant amount of ribonucleoprotein (RNP) complex and single-stranded oligodeoxynucleotide (ssODN) donor template designed to insert HiBiT at the N-terminus of Fluc via CRISPR / Cas9 into HEK293 cells stably expressing firefly luciferase (HEK293 / Fluc cells). The RNP / ssODN mixture was delivered into cells using titrations of modified PEI and PAMAM compounds at the final concentrations listed. After 2 days, cells were measured for viability using CellTiter-Fluor (CTF). [Figure 17B] Illustrates the delivery of a constant amount of ribonucleoprotein (RNP) complex and single-stranded oligodeoxynucleotide (ssODN) donor template designed to insert HiBiT at the N-terminus of Fluc via CRISPR / Cas9 into HEK293 cells stably expressing firefly luciferase (HEK293 / Fluc cells). The RNP / ssODN mixture was delivered into the cells using titrations of modified PEI and PAMAM compounds at the final concentrations listed. After 2 days, the cells were measured for Fluc expression using ONE-Glo EX. [Figure 17C] Illustrates the delivery of a constant amount of ribonucleoprotein (RNP) complex and single-stranded oligodeoxynucleotide (ssODN) donor template designed to insert HiBiT at the N-terminus of Fluc via CRISPR / Cas9 into HEK293 cells stably expressing firefly luciferase (HEK293 / Fluc cells). The RNP / ssODN mixture was delivered into cells using titrations of modified PEI and PAMAM compounds at the final concentrations listed. After 2 days, cells were measured for HiBiT signal using the HiBiT NanoDLR assay. [Figure 17D]Illustrates the delivery of a constant amount of ribonucleoprotein (RNP) complex and single-stranded oligodeoxynucleotide (ssODN) donor template designed to insert HiBiT at the N-terminus of Fluc via CRISPR / Cas9 into HEK293 cells stably expressing firefly luciferase (HEK293 / Fluc cells). The RNP / ssODN mixture was delivered into cells using titrations of modified PEI and PAMAM compounds at the final concentrations listed. The HiBiT / CTF ratio was used to normalize the HiBiT signal to cell number. [Figure 17E] Illustrates the delivery of a constant amount of ribonucleoprotein (RNP) complex and single-stranded oligodeoxynucleotide (ssODN) donor template designed to insert HiBiT at the N-terminus of Fluc via CRISPR / Cas9 into HEK293 cells stably expressing firefly luciferase (HEK293 / Fluc cells). The RNP / ssODN mixture was delivered into cells using titrations of modified PEI and PAMAM compounds at the final concentrations listed. The HiBiT / Fluc ratio was used to normalize the HiBiT signal to the amount of Fluc expression. [Figure 18]A-B illustrate pools of HEK293 / Fluc cells delivered with RNP / ssODN mixtures for CRISPR-mediated HiBiT knock-in using either nucleofection or modified PEI or PAMAM polymers. To exclude complications from cell death during the process, cell pools were grown for several days before measurement. After HiBiT knock-in at the N-terminus of Fluc, viability, Fluc expression, and HiBiT signal were measured using CellTiter-Fluor+HiBiT NanoDLR (A). The large drop in Fluc / CTF ratio for nucleofected cells may indicate loss of expression caused by InDel mutations. As shown by the HiBiT / CTF ratio, RNP / ssODN delivery mediated by modified polymers resulted in not only higher normalized Fluc expression but also higher normalized HiBiT signal. Similarly, modified PEI polymers show higher normalized HiBiT signals compared to nucleofection following delivery of an RNP / ssODN mixture designed to knock-in HiBiT at the C-terminus of GAPDH (B). [Figure 19] AB show the results of a proteolytic assay to demonstrate that the modified PEI polymers described herein deliver functional LgBiT into cells, as described in Example 6. [Figure 20A] 1 shows the results of an assay to distinguish between intracellular and extracellular light-emitting systems in a cell line (HEK293), as described in Example 7. [Figure 20B] 1 shows the results of an assay to distinguish between intracellular and extracellular light-emitting systems in a cell line (A549), as described in Example 7. [Figure 20C] 1 shows the results of an assay to distinguish between intracellular and extracellular light-emitting systems in a cell line (H1299), as described in Example 7. [Figure 20D] 1 shows the results of an assay to distinguish between intracellular and extracellular light-emitting systems in a cell line (Mia-PaCa2), as described in Example 7. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0031] Provided herein are modified polyethyleneimine polymers and modified poly(amidoamine) dendrimers for use in delivering biomolecules to cells.

[0032] The modified polymers and dendrimers, in some embodiments, contain fluorinated substituents. Fluorinated compounds are hydrophobic and lipophobic at the same time, with high phase separation tendency in both polar and non-polar environments, therefore fluorination can improve the affinity of the polymer to cell membranes and also aid in the transport of molecules across the lipid bilayer of cell membranes as well as endosomal / lysosomal membranes, facilitating the endosomal escape of the polymer. In addition, fluorinated polymers have low surface energy and preferentially associate with each other at low concentrations, allowing the formation of polymer complexes with nucleic acids or proteins at low concentrations.

[0033] The section headings used in this section and throughout this disclosure are for organizational purposes only and are not intended to be limiting.

[0034] 1.Definition Unless otherwise defined herein, scientific and technical terms used in connection with this disclosure shall have the meanings commonly understood by those skilled in the art. For example, any academic terms used in connection with cell and tissue culture, molecular biology, immunology, microbiology, genetics, and protein and nucleic acid chemistry, and hybridization described herein, and techniques thereof, are well known and commonly used in the art. The meaning and scope of the terms should be clear, but in the event of any potential ambiguity, the definitions provided herein take precedence over any dictionary or external definitions. Furthermore, singular terms shall include the plural, and plural terms shall include the singular, unless the context otherwise requires.

[0035] Definitions of specific functional groups and chemical terms are described in more detail below. For purposes of this disclosure, chemical elements are identified according to the Periodic Table of the Elements, CAS version (Handbook of Chemistry and Physics, 75th Ed., inside cover), and specific functional groups are generally defined as described therein. Additionally, general principles of organic chemistry, as well as specific functional moieties and reactivities, are described in detail in Sorrell, Organic Chemistry, 2000, pp. 111-115, 1997. nd edition,University Science Books,Sausalito,2006,Smith,March's Advanced Organic Chemistry:Reactions,Mechanism,and Structure,7 th Edition, John Wiley & Sons, Inc., New York, 2013, Larock, Comprehensive Organic Transformations, 3 rd Edition, John Wiley & Sons, Inc., New York, 2018, Carruthers, Some Modern Methods of Organic Synthesis, 3 rd Edition, Cambridge University Press, Cambridge, 1987, the entire contents of each of which are incorporated herein by reference.

[0036] The term "alkyl" as used herein refers to an alkyl group having 1 to 30 carbon atoms, e.g., 1 to 16 carbon atoms (C1 to C 16 Alkyl), 1 to 14 carbon atoms (C1 to C 14 Alkyl), 1 to 12 carbon atoms (C1 to C 12 Alkyl), 1 to 10 carbon atoms (C1 to C 10"alkyl" refers to a linear or branched saturated hydrocarbon chain containing 1 to 8 carbon atoms (C1-C8 alkyl), 1 to 6 carbon atoms (C1-C6 alkyl), or 1 to 4 carbon atoms (C1-C4 alkyl). Representative examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl, and n-dodecyl.

[0037] The term "aryl" as used herein refers to a phenyl group, or a bicyclic or tricyclic aromatic fused ring system. Bicyclic fused ring systems include those in which a phenyl group is attached to a parent molecular moiety and fused to a phenyl group. Tricyclic fused ring systems include those in which a phenyl group is attached to a parent molecular moiety and fused to two other phenyl groups. Representative examples of bicyclic aryls include, but are not limited to, naphthyl. Representative examples of tricyclic aryls include, but are not limited to, anthracenyl.

[0038] The term "cycloalkyl" as used herein refers to a saturated carbocyclic ring system containing 3 to 10 carbon atoms and 0 heteroatoms. Cycloalkyls can be monocyclic, bicyclic, bridged, fused, or spirocyclic. Representative examples of cycloalkyls include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, adamantyl, bicyclo[2.2.1]heptanyl, bicyclo[3.2.1]octanyl, and bicyclo[5.2.0]nonanyl.

[0039] The term "halogen" or "halo" as used herein means F, Cl, Br, or I.

[0040] The term "haloalkyl" as used herein refers to an alkyl group as defined herein, in which one or more hydrogen atoms are replaced by halogen.For example, one, two, three, four, five, six, seven, or eight hydrogen atoms can be replaced by halogen.Representative examples of haloalkyl include, but are not limited to, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2-fluoroethyl, 2,2-difluoroethyl, and 2,2,2-trifluoroethyl.

[0041] The term "heteroaryl" as used herein refers to an aromatic monocyclic ring or an aromatic bicyclic or tricyclic ring system. An aromatic monocyclic ring is a 5- or 6-membered ring containing at least one heteroatom independently selected from the group consisting of N, O, and S (e.g., 1, 2, 3, or 4 heteroatoms independently selected from O, S, and N). A 5-membered aromatic monocyclic ring has two double bonds, and a 6-membered aromatic monocyclic ring has three double bonds. Examples of bicyclic heteroaryl groups include those in which a monocyclic heteroaryl ring is attached and fused to a monocyclic aryl group as defined herein or a monocyclic heteroaryl group as defined herein. Examples of tricyclic heteroaryl groups include those in which a monocyclic heteroaryl ring is fused to two rings independently selected from a monocyclic aryl group as defined herein or a monocyclic heteroaryl group as defined herein. Representative examples of monocyclic heteroaryls include, but are not limited to, pyridinyl (including pyridin-2-yl, pyridin-3-yl, pyridin-4-yl), pyrimidinyl, pyrazinyl, pyridazinyl, pyrrolyl, benzopyrazolyl, 1,2,3-triazolyl, 1,3,4-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-oxadiazolyl, 1,2,4-oxadiazolyl, imidazolyl, thiazolyl, isothiazolyl, thienyl, furanyl, oxazolyl, isoxazolyl, 1,2,4-triazinyl, and 1,3,5-triazinyl. Representative examples of bicyclic heteroaryls include, but are not limited to, benzimidazolyl, benzodioxolyl, benzofuranyl, benzoxadiazolyl, benzopyrazolyl, benzothiazolyl, benzothienyl, benzotriazolyl, benzoxadiazolyl, benzoxazolyl, chromenyl, imidazopyridine, imidazothiazolyl, indazolyl, indolyl, isobenzofuranyl, isoindolyl, isoquinolinyl, naphthyridinyl, purinyl, pyridoimidazolyl, quinazolinyl, quinolinyl, quinoxalinyl, thiazolopyridinyl, thiazolopyrimidinyl, thienopyrrolyl, and thienothienyl.Representative examples of tricyclic heteroaryls include, but are not limited to, dibenzofuranyl and dibenzothienyl. Monocyclic, bicyclic, and tricyclic heteroaryls can be attached to the parent molecular moiety through any carbon atom or any nitrogen atom contained within the ring.

[0042] The term "heterocycle" or "heterocyclic" as used herein means a monocyclic heterocycle, a bicyclic heterocycle, or a tricyclic heterocycle. A monocyclic heterocycle is a 3-, 4-, 5-, 6-, 7-, or 8-membered ring containing at least one heteroatom independently selected from the group consisting of O, N, and S. A 3- or 4-membered ring contains zero or one double bond and one heteroatom selected from the group consisting of O, N, and S. A 5-membered ring contains zero or one double bond and one, two, or three heteroatoms selected from the group consisting of O, N, and S. A 6-membered ring contains zero, one, or two double bonds and one, two, or three heteroatoms selected from the group consisting of O, N, and S. The 7- and 8-membered rings contain 0, 1, 2, or 3 double bonds and 1, 2, or 3 heteroatoms selected from the group consisting of O, N, and S. Representative examples of monocyclic heterocycles include azetidinyl, azepanyl, aziridinyl, diazepanyl, 1,3-dioxanyl, 1,3-dioxolanyl, 1,3-dithiolanyl, 1,3-dithianyl, imidazolinyl, imidazolidinyl, isothiazolinyl, isothiazolidinyl, isoxazolinyl, isoxazolidinyl, morpholinyl, oxadiazolinyl, oxadiazolidinyl, oxazolinyl, oxazolidinyl, oxetanyl, piperazinyl, piperidinyl, and the like. These include, but are not limited to, pyranyl, pyrazolinyl, pyrazolidinyl, pyrrolinyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydropyranyl, tetrahydropyridinyl, tetrahydrothienyl, thiadiazolinyl, thiadiazolidinyl, 1,2-thiazinanyl, 1,3-thiazinanyl, thiazolinyl, thiazolidinyl, thiomorpholinyl, 1,1-dioxidethiomorpholinyl (thiomorpholinesulfone), thiopyranyl, and trithianyl.A bicyclic heterocycle is a monocyclic heterocycle fused to a phenyl group, or a monocyclic heterocycle fused to a monocyclic cycloalkyl, or a monocyclic heterocycle fused to a monocyclic cycloalkenyl, or a monocyclic heterocycle fused to a monocyclic heterocycle, or a spiro heterocyclic group, or a bridged monocyclic heterocyclic ring system in which two non-adjacent atoms of the ring are linked by an alkylene bridge of 1, 2, 3, or 4 carbon atoms, or an alkenylene bridge of 2, 3, or 4 carbon atoms. Representative examples of bicyclic heterocycles include, but are not limited to, benzopyranyl, benzothiopyranyl, chromanyl, 2,3-dihydrobenzofuranyl, 2,3-dihydrobenzothienyl, 2,3-dihydroisoquinoline, 2-azaspiro[3.3]heptan-2-yl, azabicyclo[2.2.1]heptyl (including 2-azabicyclo[2.2.1]hept-2-yl), 2,3-dihydro-1H-indolyl, isoindolinyl, octahydrocyclopenta[c]pyrrolyl, octahydropyrrolopyridinyl, and tetrahydroisoquinolinyl. Examples of tricyclic heterocycles include bicyclic heterocycles fused to a phenyl group, or bicyclic heterocycles fused to a monocyclic cycloalkyl, or bicyclic heterocycles fused to a monocyclic cycloalkenyl, or bicyclic heterocycles fused to a monocyclic heterocycle, or bicyclic heterocycles in which two non-adjacent atoms of the bicyclic ring are linked by an alkylene bridge of 1, 2, 3, or 4 carbon atoms, or an alkenylene bridge of 2, 3, or 4 carbon atoms. Examples of tricyclic heterocycles include octahydro-2,5-epoxypentalene, hexahydro-2H-2,5-methanocyclopenta[b]furan, hexahydro-1H-1,4-methanocyclopenta[c]furan, aza-adamantane (1-azatricyclo[3.3.1.1. 3,7 ]decane), and oxa-adamantane (2-oxatricyclo[3.3.1.1 3,7 ]decane). The monocyclic, bicyclic, and tricyclic heterocycles can be connected to the parent molecular moiety through any carbon atom or any nitrogen atom contained within the ring.

[0043] The term "perfluoroalkyl" as used herein refers to an alkyl group in which each hydrogen has been replaced with a fluorine. Representative examples of perfluoroalkyl include, but are not limited to, trifluoromethyl, perfluoroethyl, perfluoropropyl, perfluorobutyl, perfluoropentyl, and perfluorohexyl.

[0044] The term "poly(amidoamine)" (or "PAMAM") as used herein refers to a class of art-recognized dendrimers having a diamine core and repeating branched subunits with amide and amine functionalities produced by the reaction of this diamine with methyl acrylate and then another diamine. These dendrimers are defined by the number of "layers" of amidoamine groups extending from the core, with each "layer" referred to as a "generation." For example, ethylenediamine can be reacted with methyl acrylate to produce methyl 3-[2-[bis(3-methoxy-3-oxopropyl)amino]ethyl-(3-methoxy-3-oxopropyl)amino]propanoate, which can then be reacted with additional ethylenediamine to form "generation 0" PAMAM, N-(2-aminoethyl)-3-[[3-(2-aminoethylamino)-3-oxopropyl]-[2-[bis[3-(2-aminoethylamino)-3-oxopropyl]amino]ethyl]amino]propanamide. The same reaction sequence can be repeated to similarly functionalize each of the primary amino groups of the 0th generation PAMAM to form the 1st generation PAMAM, and so on. The chemical structure of the 1st generation PAMAM is shown below, with the "core" 0th generation PAMAM structure highlighted. [ka]

[0045] As used herein, the term "polyethyleneimine" (or "PEI") refers to a polymer based on repeating iminoethylene groups. "Linear polyethyleneimine" has the formula -(CH2-CH2-NH) n - and therefore contains only secondary amino groups within the polymer chain. "Branched polyethyleneimine" is a branched polymer synthesized by ring-opening polymerization of aziridine and contains primary, secondary, and tertiary amino groups. Although branched polyethyleneimine is often depicted as an example below, one skilled in the art will understand that branched polyethyleneimine is not a polymer having the exact type of repeat unit shown between the brackets, but rather, this merely provides an illustration of the various ways in which the individual -CH2-CH2-NH- groups can be linked together, with additional linkages and branching points possible. [ka]

[0046] In some cases, the number of carbon atoms in a group (e.g., alkyl, haloalkyl, or cycloalkyl) is referred to as "C x ~C y Groups are designated by the prefix "-" where x is the minimum number of carbon atoms in the group and y is the maximum number. Thus, for example, "C1-C3-alkyl" refers to an alkyl group containing 1 to 3 carbon atoms, "C1-C6-haloalkyl" refers to a haloalkyl group containing 1 to 6 carbon atoms.

[0047] The term "substituent" refers to a group substituted on an atom of a specified group.

[0048] Where a group or moiety may be substituted, the term "substituted" indicates that one or more (e.g., 1, 2, 3, 4, 5, or 6, in some embodiments 1, 2, or 3, and in other embodiments 1 or 2) hydrogens in the group designated by the phrase "substituted" may be replaced with a selection of the designated group listed, or with suitable groups known in the art (e.g., one or more of the groups listed below). Substituents include, but are not limited to, halogen, =O, =S, cyano, nitro, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkyl, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocycle, cycloalkyl, heteroarylalkyl, arylalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkylene, aryloxy, phenoxy, benzyloxy, amino, alkylamino, acylamino, aminoalkyl, arylamino, sulfonylamino, sulfinylamino, sulfonyl, alkylsulfonyl, arylsulfonyl, aminosulfonyl, sulfinyl, -COOH, ketone, amide, carbamate, and acyl.

[0049] As used herein, the terms "Oplophorus luciferase" and "Oplophorus-derived luciferase" are used interchangeably and refer to luciferase secreted from the deep-sea shrimp Oplophorus gracilirostris, including wild-type, variants and mutants thereof (e.g., SEQ ID NO: 1). For example, suitable Oplophorus luciferase variants are described in U.S. Patent Nos. 8,557,970 and 8,669,103, each of which is incorporated herein by reference in its entirety. Exemplary Oplophorus-derived luciferases include, for example, the luciferase of SEQ ID NO: 2 (also referred to interchangeably herein as "NanoLuc", "Nluc", "Nluc luciferase", and "Nluc enzyme").

[0050] For the compounds described herein, the groups and substituents may be selected based on permissible valences of atoms and substituents such that their selection and substitution result in stable compounds that do not spontaneously undergo transformations, such as by rearrangement, cyclization, elimination, and the like.

[0051] As used herein, the terms "comprise(s)", "include(s)", "having", "has", "can", "contain(s)", and variations thereof are intended to be open-ended transitional phrases, terms, or words that do not exclude the possibility of additional acts or structures. The singular forms "a", "an", and "the" include plural referents unless the context clearly dictates otherwise. Many embodiments herein are described using the open-ended "comprising" language. Such embodiments encompass multiple closed-ended "consisting of" and / or "consisting essentially of" embodiments, which may alternatively be claimed or described using such language. The present disclosure also contemplates other embodiments that "comprising", "consisting of", and "consisting essentially of" the embodiments or elements presented herein, whether or not expressly stated.

[0052] With respect to the recitation of numerical ranges herein, each intervening numerical value with the same precision is expressly contemplated. For example, in the range of 6 to 9, the numbers 7 and 8 are contemplated in addition to 6 and 9, and in the range of 6.0 to 7.0, the numbers 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, and 7.0 are expressly contemplated.

[0053] 2. Polymers The present disclosure includes modified polyamine polymers that are suitable for delivery of biomolecules, such as genes, proteins, and ribonucleoproteins, and related complexes, into cells.

[0054] In some embodiments, the present disclosure provides: A polyethyleneimine polymer; and a plurality of substituents attached to amino groups of the polyethyleneimine polymer, each substituent independently having the formula (I): -X-(CH2) n -Z (I), During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, 2, 3, 4, or 5; Compounds are provided in which Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group.

[0055] In some embodiments, the polyethyleneimine polymer has a weight average molecular weight of about 500 Da to about 250,000 Da, or about 500 Da to about 30,000 Da, or about 500 Da to about 2,000 Da, or about 5,000 Da to about 25,000 Da. For example, the polyethyleneimine polymer may be about 500 Da, about 600 Da, about 700 Da, about 800 Da, about 900 Da, about 1,000 Da, about 1,200 Da, about 1,400 Da, about 1,600 Da, about 1,200 Da, about 1,400 Da, about 1,600 Da, about 1,800 Da, about 2,000 Da, about 3,000 Da, about 4,000 Da, about 5,000 Da, about 6,000 Da, about The weight average molecular weight may be about 7000 Da, about 8000 Da, about 9000 Da, about 10000 Da, about 15000 Da, about 20000 Da, about 25000 Da, about 30000 Da, about 35000 Da, about 40000 Da, about 45000 Da, about 50000 Da, about 100000 Da, about 150000 Da, about 200000 Da, or about 250000 Da. In certain embodiments, the polyethyleneimine polymer has a weight average molecular weight of about 600 Da, about 800 Da, about 1200 Da, about 1800 Da, about 5000 Da, about 10000 Da, or about 25000 Da.

[0056] The polyethyleneimine polymer may be linear or branched. In some embodiments, the polyethyleneimine polymer is a linear polyethyleneimine polymer. In some embodiments, the polyethyleneimine polymer is a branched polyethyleneimine polymer.

[0057] In some embodiments, the polyethyleneimine polymer may be crosslinked. For example, the polyethyleneimine polymer may be crosslinked with urea before or after functionalization such that the polymer contains multiple substituents of formula (I) (i.e., two amino groups on two different polymers are linked together by a C=O group).

[0058] In the multiple substituents of formula (I), X is a bond or -C(O)-O-. In some embodiments, X is a bond. In some embodiments, X is -C(O)-O-.

[0059] In the multiple substituents of formula (I), n is 0, 1, 2, 3, 4, or 5. In some embodiments, n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In some embodiments, n is 0, 1, or 2. In some embodiments, n is 1 or 2.

[0060] In some embodiments, X is —C(O)—O— and n is 1 or 2. In some embodiments, X is a bond and n is 1 or 2.

[0061] In the multiple substituents of formula (I), Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group. In some embodiments, Z is selected from a haloalkyl group, a substituted aryl group, and an unsubstituted heteroaryl group.

[0062] In some embodiments, Z is a haloalkyl group. In some embodiments, the haloalkyl group is a perfluoroalkyl group. In some embodiments, Z is a group of the formula -(CF2) m and m is a haloalkyl group having -CF3, where m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. For example, in some embodiments, m is 1. In some embodiments, m is 2. In some embodiments, m is 3. In some embodiments, m is 4. In some embodiments, m is 5. In some embodiments, m is 6. In some embodiments, m is 7. In some embodiments, m is 8. In some embodiments, m is 9. In some embodiments, m is 10. In some embodiments, m is 3, 4, 5, 6, or 7.

[0063] In some embodiments, Z is an aryl group or a substituted aryl group. In some embodiments, Z is a substituted aryl group. In some embodiments, Z is a substituted phenyl group. In some embodiments, Z is a phenyl group substituted with 1, 2, 3, 4, or 5 substituents selected from halo. In some embodiments, Z is a pentafluorophenyl group.

[0064] In some embodiments, Z is a heteroaryl group or a substituted heteroaryl group. In some embodiments, Z is an unsubstituted heteroaryl group. In some embodiments, Z is an unsubstituted monocyclic heteroaryl group. In some embodiments, the heteroaryl group is a monocyclic heteroaryl group having 1, 2, or 3 heteroatoms independently selected from N, O, and S. In some embodiments, Z is an unsubstituted pyridyl group.

[0065] In some embodiments, X is —C(O)O— and n is 1 or 2. In some embodiments, X is a bond and n is 1 or 2.

[0066] In some embodiments, about 0.1 mol % to about 60 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I), for example, about 10 mol % to about 60 mol %, about 5 mol % to about 50 mol %, or about 8 mol % to about 40 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I). In some embodiments, about 0.1 mol%, about 0.5 mol%, about 1 mol%, about 2 mol%, about 5 mol%, about 6 mol%, about 7 mol%, about 8 mol%, about 9 mol%, about 10 mol%, about 15 mol%, about 20 mol%, about 25 mol%, about 30 mol%, about 35 mol%, about 40 mol%, about 45 mol%, about 50 mol%, about 55 mol%, about 60 mol%, about 65 mol%, about 70 mol%, about 75 mol%, or about 80 mol% of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I). The degree of modification can be adjusted, for example, by using different amounts of reagents as further discussed below. The degree of modification can be adjusted, for example, by using different amounts of reagents as further discussed below. 1 It can be determined using 1 H NMR spectroscopy.

[0067] In some embodiments, the present disclosure provides: a poly(amidoamine) dendrimer; and a plurality of substituents attached to amino groups of the poly(amidoamine) dendrimer, each substituent independently having the formula (I): -X-(CH2) n -Z (I), During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, or 2; Compounds are provided in which Z is selected from haloalkyl groups, aryl groups, substituted aryl groups, heteroaryl groups, and substituted heteroaryl groups.

[0068] In some embodiments, the poly(amidoamine) dendrimer is a 0th generation, 1st generation, 2nd generation, 3rd generation, 4th generation, 5th generation, 6th generation, 7th generation, 8th generation, 9th generation, or 10th generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a 1st generation, 2nd generation, 3rd generation, 4th generation, 5th generation, 6th generation, 7th generation, 8th generation, 9th generation, or 10th generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a 1st generation, 2nd generation, 3rd generation, or 4th generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a 1st generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a 2nd generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a third generation poly(amidoamine) dendrimer. In some embodiments, the poly(amidoamine) dendrimer is a fourth generation poly(amidoamine) dendrimer.

[0069] In the multiple substituents of formula (I), X is a bond or -C(O)-O-. In some embodiments, X is a bond. In some embodiments, X is -C(O)-O-.

[0070] In the multiple substituents of formula (I), n is 0, 1, 2, 3, 4, or 5. In some embodiments, n is 0. In some embodiments, n is 1. In some embodiments, n is 2. In some embodiments, n is 3. In some embodiments, n is 4. In some embodiments, n is 5. In some embodiments, n is 0, 1, or 2. In some embodiments, n is 1 or 2.

[0071] In some embodiments, X is a bond and n is 1.

[0072] In the multiple substituents of formula (I), Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group. In some embodiments, Z is selected from a haloalkyl group, a substituted aryl group, and an unsubstituted heteroaryl group.

[0073] In some embodiments, Z is a haloalkyl group. In some embodiments, the haloalkyl group is a perfluoroalkyl group. In some embodiments, Z is a group of the formula -(CF2) m and m is a haloalkyl group having -CF3, where m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. For example, in some embodiments, m is 1. In some embodiments, m is 2. In some embodiments, m is 3. In some embodiments, m is 4. In some embodiments, m is 5. In some embodiments, m is 6. In some embodiments, m is 7. In some embodiments, m is 8. In some embodiments, m is 9. In some embodiments, m is 10. In some embodiments, m is 3, 4, 5, 6, or 7.

[0074] In some embodiments, Z is an aryl group or a substituted aryl group. In some embodiments, Z is a substituted aryl group. In some embodiments, Z is a substituted phenyl group. In some embodiments, Z is a phenyl group substituted with 1, 2, 3, 4, or 5 substituents selected from halo. In some embodiments, Z is a pentafluorophenyl group.

[0075] In some embodiments, Z is a heteroaryl group or a substituted heteroaryl group. In some embodiments, Z is an unsubstituted heteroaryl group. In some embodiments, Z is an unsubstituted monocyclic heteroaryl group. In some embodiments, the heteroaryl group is a monocyclic heteroaryl group having 1, 2, or 3 heteroatoms independently selected from N, O, and S. In some embodiments, Z is an unsubstituted pyridyl group.

[0076] In some embodiments, X is —C(O)O— and n is 1 or 2. In some embodiments, X is a bond and n is 1 or 2.

[0077] In some embodiments, about 0.1 mol % to about 80 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I), for example, about 10 mol % to about 70 mol %, or about 20 mol % to about 70 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I). In some embodiments, about 0.1 mol%, about 0.5 mol%, about 1 mol%, about 2 mol%, about 5 mol%, about 6 mol%, about 7 mol%, about 8 mol%, about 9 mol%, about 10 mol%, about 15 mol%, about 20 mol%, about 25 mol%, about 30 mol%, about 35 mol%, about 40 mol%, about 45 mol%, about 50 mol%, about 55 mol%, about 60 mol%, about 65 mol%, about 70 mol%, about 75 mol%, or about 80 mol% of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I). The degree of modification can be adjusted, for example, by using different amounts of reagents as further discussed below. The degree of modification can be adjusted, for example, by using different amounts of reagents as further discussed below. 1 It can be determined using 1 H NMR spectroscopy.

[0078] The polymer contains functional groups that can be cationic (e.g., -NH2 can be -NH3 +(can be 0.01 to 0.5), and thus in some embodiments, salts can be formed with suitable anions. Examples of suitable inorganic anions include, but are not limited to, those derived from the following inorganic acids: hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, sulfurous acid, nitric acid, nitrous acid, phosphoric acid, and phosphorous acid. Examples of suitable organic anions include, but are not limited to, those derived from the following organic acids: 2-acetyoxybenzoic acid, acetic acid, ascorbic acid, aspartic acid, benzoic acid, camphorsulfonic acid, cinnamic acid, citric acid, edetic acid, ethanedisulfonic acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glutamic acid, glycolic acid, hydroxymaleic acid, hydroxynaphthalene carboxylic acid, isethionic acid, lactic acid, lactobionic acid, lauric acid, maleic acid, malic acid, methanesulfonic acid, mucic acid, oleic acid, oxalic acid, palmitic acid, pamoic acid, pantothenic acid, phenylacetic acid, phenylsulfonic acid, propionic acid, pyruvic acid, salicylic acid, stearic acid, succinic acid, sulfanilic acid, tartaric acid, toluenesulfonic acid, and valeric acid.In some embodiments, the compound is a hydrochloride salt.

[0079] The compounds are prepared by various methods. For example, carbamate-modified linear or branched PEI polymers or PAMAM dendrimers can be prepared by reacting with fluorinated alkyl p-nitrobenzene carbonate compounds, as illustrated in Schemes 1A, 1B, and 1C. PEI polymers and PAMAM dendrimers can also be modified by reacting with fluorinated aldehydes to form imine adducts, followed by imine reduction with NaBH4, to obtain the desired alkylated polymers, as illustrated in Scheme 2. The percentage of amine modification can be adjusted by adding different amounts of reagents. In addition, the primary amines of branched PEI can be partially protected with BOC, followed by alkylation with fluorinated alkyl halides and deprotection to generate free primary amine alkylated PEI compounds, as illustrated in Scheme 3.

[0080] In the schemes below, the following abbreviations are used: Boc is tert-butyloxycarbonyl, DCM is dichloromethane, THF is tetrahydrofuran, TFA is trifluoroacetic acid, and TIPS is triisopropylsilane. Scheme 1. Synthesis of modified polymers via carbamate modification A. Synthesis of carbamate-modified branched PEI compounds [ka] B. Synthesis of Carbamate-Modified Linear PEI Compounds [ka] C. Synthesis of first generation carbamate-modified PAMAM [ka] Scheme 2. Synthesis of modified PEI polymers via imine reduction [ka] Scheme 3. Alkylated PEI with free primary amines via BOC protection, alkylation, and deprotection [ka]

[0081] The compounds and intermediates herein can be isolated and purified by methods well known to those skilled in the art of organic synthesis. Examples of conventional methods for isolating and purifying compounds include, but are not limited to, chromatography on solid supports such as silica gel, alumina, or silica derivatized with alkylsilane groups, with optional pretreatment with activated carbon, thin layer chromatography, distillation at various pressures, sublimation under vacuum, and trituration, as described in, for example, "Vogel's Textbook of Practical Organic Chemistry" (5th edition (1989), by Furniss, Hannaford, Smith, and Tatchell, pub. Longman Scientific & Technical, Essex CM20 2JE, England).

[0082] The reaction conditions and reaction times for each of the individual steps may vary depending on the specific reactants employed and the substituents present in the reactants used. Specific procedures are provided in the Examples section. The reactions can be worked up in a conventional manner, for example by removing the solvent from the residue and further purified according to techniques generally known in the art, such as, but not limited to, crystallization, distillation, extraction, trituration, and chromatography. Unless otherwise stated, the starting materials and reagents are either commercially available or can be prepared from commercially available materials by one skilled in the art using methods described in the chemical literature. If the starting materials are not commercially available, they can be prepared by procedures selected from standard organic chemistry techniques, techniques analogous to the synthesis of structurally similar known compounds, or procedures analogous to those described in the Examples section of the above schemes or synthesis.

[0083] Routine experimentation is within the scope of the present invention, including appropriate manipulation of reaction conditions, reagents, and sequences of the synthetic route, protection of any chemical functional groups that are not compatible with the reaction conditions, and deprotection at suitable points in the reaction sequence of the method. Suitable protecting groups and methods for protecting and deprotecting different substituents using such suitable protecting groups are well known to those skilled in the art, examples of which can be found in the article entitled "Greene's Protective Groups in Organic Synthesis" (5th ed.) by PGM Wuts (John Wiley & Sons, Inc. (2014)), which is incorporated herein by reference in its entirety. The synthesis of the compounds of the present invention can be accomplished by methods similar to those described in the above synthetic schemes and specific examples.

[0084] The synthetic schemes and specific examples as described are illustrative and are not to be read as limiting the scope of the invention, as that scope is defined by the claims. All alternatives, modifications, and equivalents of the synthetic methods and specific examples are included within the scope of the claims.

[0085] Exemplary polymers that were prepared include those listed in Table 1. Further details regarding the synthesis of these polymers, including specific examples with actual and / or theoretical modification percentages, can be found in the Examples. [Table 1-1] [Table 1-2]

[0086] 3. Method Embodiments of the present disclosure include various compositions and methods used to deliver biomolecules of interest into cells, including the use of modified polyamine polymers, such as PEI and PAMAM dendrimers, to deliver one or more of a deoxyribonucleic acid (DNA) molecule, a ribonucleic acid (RNA) molecule, a peptide, a polypeptide, a protein, a ribonucleoprotein, or any combination or derivative thereof into cells, in some cases without the need for electroporation.

[0087] Compositions comprising PEI or PAMAM dendrimers as disclosed herein, or any combination thereof, can be used to deliver nucleic acid molecules into cells (e.g., gene transfection). In some embodiments, the nucleic acid is a polynucleotide comprising DNA, RNA, or combinations and derivatives thereof. The terms "nucleic acid molecule," "nucleic acid sequence," and "polynucleotide" are synonymous and are intended to encompass polymers of DNA or RNA that may be single-stranded or double-stranded and may contain non-natural or modified nucleotides. These terms include, as equivalents, analogs of either RNA or DNA made from nucleotide analogs and modified polynucleotides, such as, but not limited to, methylated and / or capped polynucleotides. Nucleic acids are typically linked via phosphate bonds to form nucleic acid sequences or polynucleotides, although many other linkages are known in the art (e.g., phosphorothioates, boranophosphates, etc.).

[0088] The one or more nucleic acid molecules may be DNA, RNA, or a combination thereof (e.g., DNA / RNA hybrid). In some embodiments, the nucleic acid molecule is a plasmid. The term "plasmid" as used herein refers to a small intracellular DNA molecule that is physically separated from chromosomal DNA and can replicate independently (i.e., as an "episom"). Plasmids naturally occur in bacteria, archaea, and other eukaryotic organisms and generally exist as small circular double-stranded DNA molecules. Synthetic plasmids are widely used in the art as vectors in molecular cloning to drive the replication of recombinant DNA sequences in host organisms. Plasmid DNA may be generated using routine molecular biology techniques, such as those described in, for example, Green and Sambrook, Molecular Cloning: A Laboratory Manual (Fourth Edition), Cold Spring Harbor Laboratory Press (June 15, 2012), or may be obtained from commercial sources.

[0089] The plasmid may be any suitable recombinant DNA or RNA plasmid that contains a heterologous nucleic acid sequence to be delivered to a target cell, either in vitro or in vivo. The heterologous nucleic acid sequence may code for a gene product (e.g., a protein) of interest, for example for the purpose of treating or preventing a disease, and may optionally be in the form of an expression cassette. The term "recombinant" refers to a polynucleotide of semi-synthetic or synthetic origin that is either not naturally occurring or is linked to another polynucleotide in an arrangement not found in nature. The term "heterologous" as used herein refers to a nucleic acid sequence obtained or derived from a genetically distinct entity from the rest of the entity to which it is compared.

[0090] In some embodiments, PEI or PAMAM dendrimers as disclosed herein can be used to deliver proteins, peptides, or antibodies into cells. For example, PEI or PAMAM dendrimers can be used to deliver (e.g., complementary) proteins or peptides (or polynucleotides thereof) that can form bioluminescent complexes, such as, but not limited to, NanoLuc (SEQ ID NO:2), HiBiT (SEQ ID NO:3), LgBiT (SEQ ID NO:4), SmBiT (SEQ ID NO:5), DarkBiT (SEQ ID NO:6), DarkBiT (SEQ ID NO:7, SEQ ID NO:8), LgTrip 3092 (SEQ ID NO:9), LgTrip 3546 (SEQ ID NO:10), LgTrip 2098 (SEQ ID NO:11), and SmTrip9 (SEQ ID NO:12). In some embodiments, complementary bioluminescent proteins or peptides can be used to tag one or more proteins or peptides of interest for subsequent evaluation or monitoring based on detection or non-detection of bioluminescence (e.g., formation of a bioluminescent complex).

[0091] According to these embodiments, proteins or peptides delivered using modified PEI or PAMAM dendrimers can be used to study protein-protein interactions, protein interference with blocking antibodies, intracellular trafficking, and biological functions of proteins or peptides. For example, peptides or proteins delivered using modified PEI or PAMAM dendrimers can form complementary proteins with target proteins tagged with other fragments for protein quantification in live cells. In one embodiment, HiBiT-tagged protein targets (e.g., proteins of interest containing HiBiT tags) can be quantified by directly delivering LgBiT in cells, thereby eliminating the need for a separate gene transfection step (e.g., BacMam transfection, nucleofection, etc.).

[0092] In some embodiments, the nucleic acid molecule is a DNA plasmid that comprises one or more nucleic acid sequences that mediate target gene editing or modification.For example, the DNA plasmid can comprise the components of CRISPR / Cas9 gene editing system, including but not limited to Cas9 gene or protein.CRISPR / Cas gene editing system has been developed to allow targeted modification of specific genes of interest in cells. CRISPR / Cas gene editing systems are based on the RNA-guided Cas9 nuclease from the clustered regularly interspaced short palindromic repeats type II (CRISPR) adaptive immune system of prokaryotes (e.g., Jinek et al., Science, 337:816 (2012); Gasiunas et al., Proc. Natl. Acad. Sci. USA, 109, E2579 (2012); Garneau et al., Nature, 468:67 (2010); Deveau et al., Annu. Rev. Microbiol., 64:475 (2010); Horvath and Barrangou, Science, 327:167 (2010); Makarova et al., Nat. Rev. Microbiol., 9,467 (2011); Bhaya et al., Nature, 327:167 (2010); See Cong et al., Annu. Rev. Genet., 45, 273 (2011); Cong et al., Science, 339:819-823 (2013); and U.S. Pat. Nos. 8,697,359, 8,795,965, and 9,322,037, all of which are incorporated by reference in their entireties.

[0093] In some embodiments, the nucleic acid is a guide RNA (gRNA) that is compatible with the CRISPR / Cas gene editing system, such as a gRNA that includes a CRISPR targeting RNA (crRNA) and a transactivating crRNA (tracrRNA). In some embodiments, the crRNA and tracrRNA components of the CRISPR / Cas system are fused into one RNA molecule to target a specific sequence of genomic DNA (gRNA is not found in nature). The crRNA sequence is generally synthesized to target the desired genomic DNA, while the tracrRNA sequence is derived from a bacterial sequence that is required to form a complex with the Cas protein. The guide RNA may also be referred to as a single guide RNA (sgRNA).

[0094] In some embodiments, the gRNA and Cas9 protein can constitute a ribonucleoprotein (RNP) complex. The RNP generally comprises purified Cas9 protein complexed with gRNA. Such RNPs can be assembled in vitro and can be directly delivered to cells using modified polyamine polymers such as PEI and PAMAM dendrimers of the present disclosure, in some cases without the need for electroporation. Cas9 RNPs can cleave genomic targets with similar efficiency compared to plasmid-based expression of Cas9 / gRNA, and can be used for most current CRISPR genome engineering applications, including but not limited to, generating single or multiple gene knockouts in a wide variety of cell types, gene editing using homologous sequence-dependent repair (HDR), and generating large genomic deletions.

[0095] In some embodiments, Cas9 RNP is delivered into cells using modified polyamine polymers such as PEI and PAMAM dendrimers to facilitate the insertion of a luminescent peptide or polypeptide tag on a protein of interest in the cell, as further disclosed herein. In some embodiments, delivery of such RNP into cells can result in expression of the protein of interest and the luminescent tag (e.g., as measured by the luminescence of the tag) and / or the production of clones that exhibit stable expression of the protein of interest and the luminescent tag. For example, Cas9 RNP can include Cas9 protein, gRNA, and donor DNA template. The donor DNA template can include a polynucleotide that encodes a peptide or polypeptide capable of luminescence activity, as well as genomic sequences (e.g., homology arms) that facilitate the insertion of the peptide or polypeptide near the endogenous protein of interest. RNPs that include Cas9 protein, gRNA, and donor DNA template can be incorporated into compositions that include modified polyamine polymers of the present disclosure to facilitate delivery into cells for both transient and stable quantification of protein expression (e.g., luminescence).

[0096] In some embodiments, the donor DNA template contains a sequence encoding HiBiT (SEQ ID NO: 3), an 11 amino acid polypeptide that can generate high-brightness, quantitative luminescence through high-affinity complementation with the 18 kDa subunit (LgBiT) derived from NanoLuc. According to these embodiments, RNPs with donor DNA containing a sequence encoding HiBiT can be delivered into cells using modified polyamine polymers of the present disclosure. In some embodiments, a luminescent substrate and LgBiT (SEQ ID NO: 4) are added to cell lysates or directly delivered into cells using modified polyamine polymers of the present disclosure to generate luminescence. Complementation of HiBiT and LgBiT in the presence of the substrate generates a luminescent signal that is proportional to the expression of the protein of interest. In some cases, delivery of RNPs and / or luminescent peptides or polypeptides into cells by modified polyamine polymers of the present disclosure obviates the need to use other delivery methods, such as electroporation, without causing significant cytotoxicity.

[0097] In some embodiments, the donor DNA template contains a sequence encoding an 11 amino acid polypeptide (e.g., SmBiT (SEQ ID NO: 5)) that can generate high-brightness, quantitative luminescence through high-affinity complementation with an 18 kDa subunit (e.g., LgBiT) derived from NanoLuc. According to these embodiments, RNPs with donor DNA containing a sequence encoding SmBiT can be delivered into cells using modified polyamine polymers of the present disclosure. In some embodiments, to generate luminescence, a luminescent substrate and LgBiT (SEQ ID NO: 4) are added to cell lysates or directly delivered into cells using modified polyamine polymers of the present disclosure. Complementation of SmBiT and LgBiT in the presence of the substrate generates a luminescent signal that is proportional to the expression of the protein of interest. In some cases, delivery of RNPs and / or luminescent peptides or polypeptides into cells by modified polyamine polymers of the present disclosure obviates the need to use other delivery methods, such as electroporation, without causing significant cytotoxicity.

[0098] In some embodiments, the donor DNA template comprises a sequence encoding any of the peptides or polypeptides disclosed in U.S. Patent No. 9,797,890, which is incorporated herein by reference in its entirety for all purposes. For example, the donor template may comprise a polynucleotide encoding a peptide or polypeptide comprising a single amino acid difference with MGVTGWRLCERILA (SEQ ID NO: 8). In some embodiments, the donor template may comprise a polynucleotide encoding a peptide or polypeptide comprising two or more (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, etc.) amino acid differences with MGVTGWRLCERILA (SEQ ID NO: 2), or any other peptide or polypeptide disclosed in U.S. Patent No. 9,797,890.

[0099] In some embodiments, the donor DNA template comprises a sequence encoding any of the peptides or polypeptides disclosed in U.S. Provisional Patent No. 62 / 684,014, which is incorporated herein by reference in its entirety for all purposes. For example, the donor template may comprise a polynucleotide encoding a peptide or polypeptide that contains a single amino acid difference from the amino acid of LgTrip 3092 (SEQ ID NO: 9), LgTrip 3546 (SEQ ID NO: 10), LgTrip 2098 (SEQ ID NO: 11), or SmTrip9 (SEQ ID NO: 12). In some embodiments, the donor template may comprise a polynucleotide encoding a peptide or polypeptide that contains two or more (e.g., 2, 3, 4, 5, 6, 7, 8, 9, 10, etc.) amino acid differences from SEQ ID NOs: 9-12, or any other peptide or polypeptide disclosed in U.S. Provisional Patent No. 62 / 684,014.

[0100] Embodiments of the present disclosure also include identifying optimal modified PEI or PAMAM concentrations, or combinations thereof, at optimal concentrations for a biomolecule of interest that can provide acceptable results, for example, in relation to transfection efficiency and toxicity levels. These ratios or concentrations may be empirically determined and will depend on a variety of factors, including, but not limited to, the percentage of amines modified in the PEI and PAMAM, the biomolecule of interest (e.g., polynucleotide, polypeptide), cell type, cell density, nature of the assay, etc. In some embodiments, the optimal concentration is in the nM to μM range. In some embodiments, the optimal concentration is in the 1 μM to 20 μM range.

[0101] Cells that can be used with the compositions and methods of the present disclosure include any suitable prokaryotic or eukaryotic cells. Suitable cells may include cells that can be easily and reliably grown, cells that have a reasonably fast growth rate, cells that have a well-characterized expression system, and cells that can be easily and efficiently transformed or transfected. Examples of suitable prokaryotic cells include, but are not limited to, cells from the genera Bacillus (such as Bacillus subtilis and Bacillus brevis), Escherichia (such as E. coli), Pseudomonas, Streptomyces, Salmonella, and Erwinia. Particularly useful prokaryotic cells include various strains of Escherichia coli, such as K12, HB101 (ATCC No. 33694), DH5a, DH10, MC1061 (ATCC No. 53338), and CC102. Suitable eukaryotic cells are known in the art and include, for example, yeast cells, insect cells, and mammalian cells, including primary and transformed cells. In some embodiments, the cell is a mammalian cell. Several suitable mammalian host cells are known in the art and many are available from the American Type Culture Collection (ATCC, Manassas, VA). Examples of suitable mammalian cells include, but are not limited to, Chinese Hamster Ovary Cells (CHO) (ATCC No. CCL61), CHO DHFR cells (Urlaub et al, Proc. Natl. Acad. Sci. USA, 97:4216-4220 (1980)), human embryonic kidney (HEK) 293 or 293T cells (ATCC No. CRL1573), and 3T3 cells (ATCC No. CCL92). Other suitable mammalian cell lines are the monkey COS-1 (ATCC No. CRL1650) and COS-7 cell lines (ATCC No. CRL1651), as well as the CV-1 cell line (ATCC No. CCL70).

[0102] The present disclosure also includes a kit that includes various components described herein. For example, the kit may include any of the modified polyamine polymer compounds or salts thereof described herein, together with a container and / or instructions. The kit may also include at least one of a DNA molecule, an RNA molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof. In some embodiments, the kit includes a peptide or polypeptide of Cas9 protein. In some embodiments, the kit includes a donor DNA template that includes a sequence that codes for a luminescent peptide or polypeptide (e.g., HiBiT, LgBiT). In some embodiments, the kit includes a gRNA. In some embodiments, the kit includes an RNP complex, including, for example, a peptide or polypeptide of Cas9 protein, a donor DNA template that includes a sequence that codes for a luminescent peptide or polypeptide (e.g., HiBiT, LgBiT), and a gRNA. EXAMPLES

[0103] It will be readily apparent to those skilled in the art that other suitable modifications and adaptations of the disclosed methods described herein are readily applicable and recognizable, and can be made using suitable equivalents without departing from the scope of the disclosure or the aspects and embodiments disclosed herein. Having described the disclosure in detail above, the same will be more clearly understood with reference to the following examples, which are intended to merely illustrate some aspects and embodiments of the disclosure, and should not be considered as limiting the scope of the disclosure. The disclosures of all journal references, U.S. patents, and publications referenced herein are hereby incorporated by reference in their entirety.

[0104] The present disclosure has multiple aspects, illustrated by the following non-limiting examples.

[0105] In these examples, the following abbreviations are used: Boc is tert-butyloxycarbonyl, DMEM is Dulbecco's modified Eagle's medium, DMF is N,N-dimethylformamide, EtOH is ethanol, FBS is fetal bovine serum, MeOH is methanol, and THF is tetrahydrofuran.

[0106] Example 1 compound synthesis I. Carbamate Modification Synthesis of fluorinated alkyl p-nitrobenzene carbonates. [ka]

[0107] To a solution of fluorinated alcohol (1 eq.) and p-nitrobenzene chloroformate (1.5 eq.) in dry THF was added dry pyridine (3 eq.) at 0° C. The mixture was stirred at room temperature overnight. After removing the white solid by filtration, the filtrate solvent was evaporated and the residue was purified by silica column using heptane / ethyl acetate as eluent to give the desired compound in 80-90% yield.

[0108] 4-Nitrophenyl (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl) carbonate (WZ-0845): 1 H NMR (CD2Cl2, δ ppm): 8.31 (d, 2H), 7.46 (d, 2H), 4.62 (t, 2H, CH2O), 2.69 (m, 2H, CH2). MS (m / e) [M+H] (C 15 H8F 13 NO5): Calculated value 529.21, observed value 529.4.

[0109] 4-Nitrophenyl(3,3,4,4,5,5,6,6,6-nonafluorohexyl) carbonate (WZ-0921). 1H NMR (CD2Cl2, δ ppm): 8.33 (d, 2H), 7.47 (d, 2H), 4.64 (t, 2H, CH2O), 2.70 (m, 2H, CH2). MS (m / e) [M+H] (C 13 H8F9NO5): Calculated 429.19, Observed 430.2.

[0110] 4-Nitrophenyl (2,2,3,3,4,4,5,5,6,6,6-undecafluorohexyl) carbonate (WZ-0851). 1 H NMR (CD2Cl2, δ ppm): 8.34 (d, 2H), 7.47 (d, 2H), 4.84 (t, 2H, CH2). MS (m / e) [M+H] (C 13 H6F 11 NO5): Calculated value 465.18, observed value 465.2.

[0111] 4-Nitrophenyl(2,2,3,3,4,4,5,5,5-nonafluoropentyl)carbonate (WZ-0886). 1 H NMR (CD2Cl2, δ ppm): 8.34 (d, 2H), 7.47 (d, 2H), 4.85 (t, 2H, CH2). MS (m / e) [M+H] (C 12 H6F9NO5): Calculated 415.17, Observed 415.3.

[0112] 4-Nitrophenyl(3,3,4,4,5,5,5-heptafluoropentyl)carbonate (WZ-0887). 1 H NMR (CD2Cl2, δ ppm): 8.32 (d, 2H), 7.45 (d, 2H), 4.64 (t, 2H, CH2O), 2.68 (m, 2H, CH2). MS (m / e) [M+H] (C 12 H8F7NO5): Calculated 379.19, Observed 379.2.

[0113] Synthesis of carbamate modified PEI 7677. As shown in Scheme 4, to four vials containing a solution of PEI (MW 800) and 150 mg (3.49 mmol of monomer) in 5 ml THF / 1 ml MeOH, 0.1 g / ml of 4-nitrophenyl (3,3,4,4,5,5,6,6,6-nonafluorohexyl) carbonate (WZ-0850), THF solution was added in amounts corresponding to molar percentages of monomer of 16% (0.24 g, 0.56 mmol), 27% (0.40 g, 0.94 mmol), 42% (0.63 g, 1.46 mmol), and 53% (0.79 g, 1.84 mmol), respectively. The resulting solution was stirred for 2 days. The four individual solutions were then transferred to four Float-A-Lyzer G2 dialysis devices (0.5-1.0 kD, 10 ml) and dialyzed sequentially with MeOH, 0.02 M HCl in MeOH, and 0.02 M HCl in HO for three days. The mixtures were further transferred to four tubes containing t-butanol (10 ml). The four resulting mixtures were filtered into four vials, and the filtrates were freeze-dried for two days to obtain white powders 7667-a-1, 7667-a-2, 7667-a-3, and 7667-a-4 with four different theoretical modification percentages. 1 The actual modification percentages obtained by 1 H NMR were 10.2%, 16.4%, 22.0%, and 30.0%, respectively. Scheme 4. Synthesis of carbamate-modified No. 7667. [ka] [Table 2]

[0114] Other carbamate-modified branched PEI, linear PEI, or PAMAM were prepared by using similar methods described for 7667. The theoretical and actual modification percentages for PEI monomer or PAMAM primary amines are listed in Table 2. [Table 3-1] [Table 3-2] [Table 3-3] [Table 3-4] [Table 3-5]

[0115] II. Imine reductive modification Synthesis of PEI 7636 modified by imine reduction. As shown in Scheme 5, to four vials containing a solution of 100 mg (2.33 mmol of monomer) of PEI (MW 800) in 2 ml of MeOH, a solution of 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctanal (0.5 g / ml) in THF was added in amounts corresponding to molar percentages of monomer of 16% (0.135 g, 0.37 mmol), 21% (0.181 g, 0.50 mmol), 27% (0.226 g, 0.62 mmol), and 38% (0.315 g, 0.87 mmol), respectively. The resulting solutions were stirred overnight. To the four corresponding solutions above, 43 mg, 57 mg, 71 mg, 85 mg, and 99 mg of NaBH4 were slowly added at 0 °C, respectively. The mixture was stirred at room temperature for 2 hours until the bubbles disappeared. The four individual solutions were then transferred into four Float-A-Lyzer G2 dialysis devices (0.5-1.0 kD, 10 ml) and dialyzed sequentially with MeOH, 0.02 M HCl in MeOH, and 0.02 M HCl in H2O for 3 days. The mixtures were transferred into four different tubes containing t-butanol (10 ml). The four resulting mixtures were filtered into four vials, and the filtrates were freeze-dried for 2 days to obtain pale yellow powders 7636-b-1, 7636-b-2, 7636-b-3, and 7636-b-4 with four different theoretical modification percentages. Scheme 5. Synthesis of modified PEI 7636-b via imine reduction. [ka] [Table 4]

[0116] Other imine reduction modified branched PEIs were prepared by using similar methods described for 7636. The theoretical modification percentages for the PEI monomers are listed in Table 3. [Table 5-1] [Table 5-2]

[0117] Pentafluorobenzyl-modified PEI 7669 and 7677 and pyridine methyl-modified PEI 7676 can be prepared via imine reduction by using similar methods. The theoretical and actual modification percentages of PEI monomers are listed in Table 4. [ka] [Table 6-1] [Table 6-2]

[0118] III. Alkylated PEI via BOC protection, alkylation, and deprotection. BOC-protected PEI. 2.5 g (58.1 mmol monomer) of PEI 1200 or PEI 25000 and NaHCO3 were dissolved in 20 ml of THF / 40 water. To a solution of 20 ml of BOC anhydride (5.07 g, 23.3 mmol), THF was added at 0°C. The mixture was stirred at room temperature overnight. Then, the mixture was heated to 65°C overnight. TLC confirmed the complete disappearance of BOC anhydride by iodine staining. After removing THF, the solution was frozen and dried by lyophilization. BOC-protected PEI was obtained. 1 Confirmed by 1 H NMR.

[0119] Alkylation of BOC-protected PEI. BOC-PEI (0.20 g, 4.65 mmol) was suspended in EtOH or DMF. To this mixture, 1,1,1,2,2,3,3,4,4-nonafluoro-6-iodohexane was added in amounts equivalent to 30%, 40%, and 50% PEI monomer, and the resulting mixture was heated to 95° C. for 48 hours. After removing the EtOH, the residue from each reaction was triturated with ether or ether was poured into each of the individual reaction DMF solutions and the solvent was removed by centrifugation. The pale yellow solid from each reaction was then washed with ether, centrifuged two more times, and dried under vacuum. Alkylated BOC-PEI was confirmed by FNMR.

[0120] Deprotection of alkylated BOC-PEI. 12 ml of TFA / DCM (1:1) was added to each of the above white solids in the presence of TIPS (0.1 ml). The mixture was stirred at room temperature for 3 h. After removing the solvent, the remaining solid was triturated with ether, centrifuged three times, and dried under vacuum. The solid was dissolved in water and dialyzed in H2O three times for 3 days. The solution was lyophilized to obtain a pale yellow powder. The modification percentage was calculated by HNMR and FNMR using CF3CH2OH as an internal control (Table 5). [Table 7]

[0121] Example 2 Gene delivery by modified PEI polymers HEK293 cells were cultured at 1.5 × 10 in 100 μl of DMEM / FBS. 5 Cells were plated at 1000 cells / ml and transfected the next day with 10 ng / well of TK / NanoLuc® expression construct (Promega Catalog No. N1501) diluted in 90 ng / well of carrier DNA (Promega Catalog No. E4881). Cells were transfected with various modified PEI polymers at different concentrations and compared to a standard 3:1 ratio FuGENE HD positive control (Promega Catalog No. E2311) and a buffer-only negative control. These conditions provided a wide dynamic range for measuring transfection efficiency by addition of Nano-Glo® Luciferase Assay Reagent (Promega Catalog No. N1110) 24 hours after transfection. In some cases, transfections were also performed in medium lacking serum, with serum being added back in several hours after transfection. Toxicity was measured by adding reconstituted CellTiter-Glo® Reagent (Promega Catalog No. G7570) to replicate wells.

[0122] Rather than using a weight-to-weight ratio, a 9:1 ratio of PEI monomer (N atom) to DNA phosphorus atom was initially chosen as the default 1x concentration. This ratio affects both transfection efficiency and toxicity. Different concentrations of PEI used relative to the standard 1x molar concentration are reported.

[0123] Initial experiments with this fixed ratio of monomer to DNA showed that the modified PEI polymers could be just as effective as FuGENE HD in transfecting HEK293 cells. As shown in Figure 1A, transfection efficiency, as measured by NanoLuc® expression, could be as high as FuGENE HD for some of the compounds, while no DNA uptake was observed in the absence of the reagent. The degree of modification of the base polymer has a significant effect on both transfection efficiency and toxicity, highlighting the importance of fine-tuning chemical synthesis in this application. At least at this constant ratio of PEI monomers, compounds based on the 800 Da polymer were more effective than those based on the 25,000 Da polymer, of which 7636-2 and 7633-5 performed particularly well. PEI compounds based on the 25,000 Da polymer generally showed lower relative transfection and appeared to be more sensitive to the presence of serum during transfection, while with the 800 Da polymer this effect was less.

[0124] Cell viability data are shown in Figure 1 B. Most compounds were well tolerated.

[0125] Further experiments demonstrated that it is possible to improve transfection efficiency or reduce toxicity using additional modification groups, especially compared to the MW 800Da polymer starting material, which showed negligible transfection and high toxicity. As can be seen in Figure 2, the 25,000Da polymer without modification already shows relatively high transfection efficiency and low toxicity. The modified 25,000Da polymers of the 7669 series were also very effective at all modification levels. On the other hand, the 7666 series showed reduced efficiency with increasing levels of modification. In the case of 7666-1, increasing the polymer to DNA ratio reduces transfection efficiency. However, with 7667-2, based on the 800Da polymer, efficient transfection was only seen at a concentration at least twice that of the standard 1x condition. 7636-2, 7676-3, and 7677-2 all gave good results at 1x concentration.

[0126] To better determine the optimal concentration of the various compounds, titrations of various modified PEIs were added to a fixed amount of DNA and used to transfect HEK293 cells. The data are shown in Figure 3, where Figure 3A shows data in the presence of serum and Figure 3B shows data in the absence of serum. Figure 3C shows cell viability as measured using the CellTiter-Glo® Luminescent Cell Viability Assay (Promega Catalog No. G7570) in the presence of serum. In the legend, MW800 and MW25000 refer to unmodified PEI polymers of the indicated molecular weights. In this figure, a relative PEI concentration of 1 indicates a default 9 to 1 ratio of PEI monomer to DNA phosphorus. This experiment identified the optimal molar ratio of PEI monomer to DNA for each compound when comparing transfection efficiency. At twice the standard ratio, both 7636-2 and 7667-4 showed higher transfection efficiency than FuGENE HD without significant toxicity. In the absence of serum, 7676-1 was also able to compare to FuGENE HD.

[0127] A panel of polymers, including PEI polymers of different molecular weights or PAMAM polymers, was used to transfect nine cell lines at different polymer concentrations: HEK293, HeLa, MDA-MB-231, HepG2, A375, HCT116, U2-OS, Jurkat, and A549 cells were transfected at 1.0 × 10 in 100 μl of DMEM / FBS (HEK293, HeLa, MDA-MB-231, HepG2, A375, HCT116, U2-OS), RPMI / FBS (Jurkat), or F12 / FBS (A549). 5 Cells were plated at 1000 cells / ml and transfected the next day with 10 ng / well of TK / NanoLuc® expression construct (Promega Catalog No. N1501) diluted in 90 ng / well of carrier DNA (Promega Catalog No. E4881). Cells were transfected with various modified PEI or PAMAM polymers at different concentrations and compared to FuGENE HD and ViaFect™ positive controls (Promega Catalog Nos. E2311 and E4981) at a 3:1 ratio as well as a buffer-only negative control. These conditions provided a wide dynamic range for measuring transfection efficiency by addition of Nano-Glo® Luciferase Assay Reagent (Promega Catalog No. N1110) 24 hours after transfection (Figures 4A-4I). Toxicity was measured by adding reconstituted CellTiter-Glo® Reagent (Promega Catalog No. G7570) to replicate wells (Figures 5A-5H). At optimal concentrations, the third generation PAMAM polymer, 7767-4, exceeded or effectively matched the performance of ViaFect™ and FuGENE HD controls for NanoLuc® expression levels for all cell lines.

[0128] To further explore the ability of PAMAM polymers to transfect a wide variety of cell types, titrations of PAMAM polymers of different sizes and modification levels were used to transfect five different cell lines (Figures 6-9). HEK293, HeLa, MDA-MB-231, HepG2, and Jurkat cells were transfected at 1.5 x 10 6H / mL in 100 μl of DMEM / FBS (all cell types except Jurkat were plated in RPMI / FBS). 5 Cells were plated at 1000 cells / ml and transfected the next day with 10 ng / well of TK / NanoLuc® expression construct (Promega Catalog No. N1501) diluted in 90 ng / well of carrier DNA (Promega Catalog No. E4881). Cells were transfected with titrations of various PAMAM polymers: 7766(-1 to -4), 7767(-1 to -4), and 7768-1b (Figures 6 and 7), and 7768(-2 to -4), 7825(-1 to -4), and 7826(-1 to -4) (Figures 8 and 9). FuGENE HD and ViaFect™ (Promega Catalog Nos. E2311 and E4981) were used in a 3:1 ratio as positive controls, and buffer alone was used as a negative control. Transfection efficiency was measured using the Nano-Glo® Luciferase Assay (Promega Cat. No. N1110) 24 hours after transfection (Figures 6A-6E and 8A-8E). Toxicity was measured by adding reconstituted CellTiter-Glo® Reagent (Promega Cat. No. G7570) to replicate wells for all cells except HeLa (Figures 7A-7D and 9A-9D). The degree of polymer modification had an effect on optimal concentration and transfection efficiency. 7767-4 again showed effective transfection of all cell types over a wide range of concentrations, while the less modified versions 7767-2 and 7767-3 required higher concentrations but were able to deliver similar or even higher amounts of DNA than 7767-4.

[0129] Example 3 LgBiT delivery This example involved CRISPR-mediated tagging as generally described in Schwinn et al., "CRISPR-Mediated Tagging of Endogenous Proteins with a Luminescent Peptide" (ACS Chem. Biol. 2018, 13, 467-474). HiBiT-edited cells were generated by CRISPR and clones were isolated by single-cell sorting. Clones were plated at 10,000 cells per well in 96-well plates. After 24 hours, cells were transfected with different complexes of modified PEI (1 μg / ml) and LgBiT protein (170 nM). Complexes were prepared by incubating modified PEI (100 μg / ml) with LgBiT (17 μM) for 30 minutes at room temperature in Opti-MEM I reduced serum medium. Cells treated with 10% BacMam-LgBiT to transduce the CMV / LgBiT expression construct served as benchmark controls. After 24 hours, cells were treated with DarkBiT (SEQ ID NO: 6 or SEQ ID NO: 7), a peptide with high affinity for LgBiT (LgBiT / DarkBiT complex produces little or no luminescence) (1 μM) to quench the luminescence activity of extracellular LgBiT. After 1 hour, cells were assayed using the Nano-Glo® Live Cell Assay System (Promega Catalog No. N2011) and CellTiter-Glo® 2.0 Assay (Promega Catalog No. G7570). Luminescence was measured with a GloMax® Discover. Data was analyzed with Prism 5.0 software (GraphPad). Results are shown in Figures 10-11.

[0130] The brightness of the luminescence signal is proportional to the amount of intracellular LgBiT being delivered, which can be correlated with the efficiency of protein uptake. In general, large size PEI (MW=25,000), with or without modification, performed better in LgBiT delivery than their respective small size counterparts (MW=800). Modified large size PEI performed better than unmodified PEI. Among the top hits, 7666-3, 7668-1, 7669-2, 7675-1, and 7709-3 performed best in facilitating LgBiT uptake across five different HiBiT clones (Figures 10 and 11). Of the six best candidates, 7669-2 and 7675-1 caused slight cytotoxicity. No toxicity was observed with 7666-3, 7668-1, and 7709-3 (Figures 11A and 11B).

[0131] HDAC2-HiBiT and HDAC6-HiBiT clones of HeLa cells were plated at 25,000 cells per well in 8-well chamber slides. After 24 h, cells were transfected with different complexes of PEI (1 μg / ml) and LgBiT protein (170 nM). Complexes were prepared by incubating 17 μM LgBiT with 100 μg / ml 7666-4, 7668-1, or 7669-2 in Opti-MEM I reduced serum medium for 30 min at room temperature. After 24 h, cells were switched to CO2-independent medium and Nano-Glo® live cell substrate was added. Cells were imaged with a bioluminescence imager (Figures 12A-12C).

[0132] HiBiT-edited HeLa or HEK293 cells were plated at 10,000 cells / well in wells of a 96-well plate. After 24 hours, cells were transfected with different complexes of PEI (modified and unmodified, 5ug / ml) and LgBiT protein (200nM). Complexes were prepared by incubating PEI with LgBiT for 30 minutes at room temperature in Opti-MEM reduced serum medium. Cells treated with 10% BacMam-LgBiT to transduce the CMV-LgBiT expression construct served as a control. After 24 hours, cell medium was replaced and cells were assayed using the NanoGlo® Live Cell Assay System (Promega Cat. No. N2011) and CellTiter-Glo® 2.0 Assay (Promega Cat. No. G7570). Luminescence was measured with a GloMax® Discover. Figure 13A illustrates the percentage of LgBiT protein delivered compared to LgBiT protein delivered via BacMam transduction. The brightness of the luminescence signal is proportional to the amount of intracellular LgBiT delivered to cells, which can be correlated with the efficiency of protein uptake. Figure 13B illustrates the percentage of live cells compared to untreated cells.

[0133] HiBiT-edited HeLa or HEK293 cells were plated at 25,000 cells / well in 400uL in 8-chamber slides. After 24 hours, cells were transfected with PBI-7666-3·LgBiT complexes. Complexes were prepared by incubating 2uM LgBiT with 100ug / mL PBI-7666-3 in Opti-MEM I reduced serum medium for 30 minutes at room temperature. 40 microliters of complexes were added to each well. After 24 hours, cells were switched to CO2-independent medium and NanoGlo® Live Cell Substrate (Promega Cat# N2011) was added. Cells were imaged with a bioluminescence imager. Cells treated with 10% BacMam-LgBiT to transduce the CMV-LgBiT expression construct served as a control. Figure 14A shows images of CASP3-HiBiT and EGFR-HiBiT clones of HeLa cells. Figure 14B shows images of GSK3b-HiBiT and HDAC6-HiBiT clones of HeLa cells, and Figure 14C shows images of HDAC2-HiBiT clones of HeLa cells and CDK11-HiBiT clones of HEK293 cells.

[0134] Example 4 HaloTag-LgBiT delivery HeLa cells were plated at 25,000 cells per well in 8-well chamber slides. After 24 hours, cells were transfected with different complexes of PEI (1 μg / ml) and HaloTag-LgBiT protein (200 nM). Complexes were prepared by incubating PEI (100 μg / ml) with HaloTag-LgBiT (20 μM) for 30 minutes at room temperature in Opti-MEM I reduced serum medium. After 24 hours, cells were switched to Opti-MEM I reduced serum medium and then incubated with HaloTag® Oregon Green® ligand (1 μM) for 30 minutes. Cells were washed three times with Opti-MEM I reduced serum medium. The final wash was performed by incubating cells in medium at 37° C. under 5% (v / v) CO2(g) for 30 minutes. For the final 5 min, cells were counterstained with the nuclear probe NucBlue® Live ReadyProbes® reagent at 37° C. Cells were imaged with a C2 laser scanning confocal microscope (Nikon).

[0135] The green fluorescence intensity is proportional to the amount of intracellular HaloTag-LgBiT being delivered, which can be correlated with the efficiency of protein uptake. Modified large size PEI (MW=25000) was better than unmodified PEI in delivering HaloTag-LgBiT. Among the top hits, 7636-2, 7637-3, 7666-3, 7668-1, and 7676-5 performed best (Figures 15A-15C). Of these, three were also the best candidates for LgBiT delivery (7666-3 and 7668-1), suggesting that cargo size influences uptake efficiency.

[0136] Punctate staining was observed in all treatments, indicating that the majority of HaloTag-LgBiT protein resides in endosomes. The brightness in endosomes created technical difficulties in quantifying the portion of protein that was released into the cytosol.

[0137] Example 5 RNP delivery HiBiT knock-in at the C-terminus of GAPDH in HEK293 cells. Preparation of RNP complex assembly and electroporation of the complex into cells were performed as previously described (Schwinn et al., "CRISPR-Mediated Tagging of Endogenous Proteins with a Luminescent Peptide," ACS Chem. Biol. 2018, 13, 467-474). Briefly, tracer and guide RNA duplexes (up to 24 μM) were prepared in a reaction volume of 5 μl, then combined with 5 μl of Cas9 (20 μM) and further incubated for 10 min at room temperature. For HEK293, cells (2 × 10 5 ) was resuspended in 20 μl of 4D Nucleofector solution SF. Then, RNP complex (10 μl) and donor DNA (1 μl containing 100 μM single-stranded oligodeoxynucleotide (ssODN)) were added to the cells. The donor DNA was designed to add the VS-HiBiT sequence to the C-terminus of the GAPDH gene. The cells were electroporated with the 4D Nucleofector system. The cells were then incubated at room temperature for 5 min and transferred to a 6-well plate for culture.

[0138] For initial RNP delivery experiments using modified PEI, a similar procedure was used. Briefly, RNP mixture (10 μl containing 12 μM double-stranded guide RNA and 10 μM Cas9) was prepared as described above. Donor DNA (1 μl containing 100 μM) was added to the RNP mixture, and the mixture was then made up to 98 μl with Opti-MEM I reduced serum medium. Modified PEI 7667-4 (2 μl containing 10 mg / ml) was then added to the RNP reaction and incubated at room temperature for 30 min. The complex (100 μl) was then transferred to cells (2×10 in 1.9 ml serum-free medium). 5) and transferred to 6-well plates for culture. Cells were placed in serum-free medium for 1 hour. Cells were then supplemented with FBS (10%) for growth and assay. After 24-48 hours, edited cells were assayed using Nano-Glo® HiBiT lytic reagent and CellTiter-Glo® 2.0. The percentage of live cells was calculated compared to untreated cells using the CellTiter-Glo® Luminescent Cell Viability Assay (Promega Cat. No. G7570) (Figure 16B).

[0139] The HiBiT luminescence signal normalized to the number of viable cells should be proportional to the efficiency of HiBiT insertion in the GAPDH locus, which can be correlated with the efficiency of RNP delivery. Nucleofection was expected to provide the most efficient RNP / ssODN delivery. As shown in Figure 16A, nucleofection showed higher knock-in efficiency than FuGENE HD, ViaFect™, CRISPRMax, or 7667-4 at initial conditions. However, even without optimizing modified PEI compounds or delivery conditions, 7667-4 produced much better RNP delivery efficiency than FuGENE HD and ViaFect™, and only slightly lower than CRISPRmax.

[0140] A model system to measure HiBiT knock-in, target expression, and viability in the same sample. To screen many compounds and delivery conditions, a more communicative plate-based system was needed. HiBiT was knocked in at the N-terminus of the firefly luciferase (Fluc) gene in a HEK293 / CMV-Fluc stable cell line. A gRNA was designed that generated a double-stranded break within the initiating methionine codon such that repair by non-homologous end joining (NHEJ) would tend to generate an insertion / deletion (InDel) mutation that knocks out expression, while homologous sequence-dependent repair (HDR) would generate a HiBiT signal and retain the Fluc signal (Diagram 1A). CellTiter-Fluor (Promega Cat. No. G6080) was multiplexed to measure cell viability such that both the Fluc and HiBiT signals could be normalized to the fluorescence of viable cells. Using the normalized ratios for Fluc and HiBiT signals, it was possible to estimate the degree of Fluc knockout by InDel mutation and HiBiT knock-in by HDR.

[0141] When optimizing conditions for delivery of RNP / ssODN to cells using modified PEI and PAMAM polymers, various concentrations of RNP, ssODN, and polymer were used. Frequently, 1.25 μM Cas9 was incubated with 1.5 μM gRNA for 10 min at room temperature to generate RNP. Donor ssODN and modified PEI or PAMAM polymer were then added to generate an 11x solution with 250 nM RNP, 1 μM ssODN, and 22-110 μg / ml polymer. After 30 min incubation at room temperature, the complexes are added to the cells and they are diluted 11x in medium (e.g., 10 μl + 100 μl medium in a 96-well plate). After 2 days, HEK293 / Fluc cells were analyzed by replacing the cell medium with OptiMEM-I containing CellTiter-Fluor reagent (Promega catalog number G6080) to measure the number of viable cells in the wells (Figure 17A). Fluc expression was measured using ONE-Glo EX (Figure 17B), and HiBiT signal was measured using HiBiT NanoDLR assay (Figure 17C). HiBiT signal was normalized to cell number using HiBiT / CTF ratio (Figure 17D). Fluc and HiBiT signal in the wells were then quantified using Nano-Glo® HiBiT Dual-Luciferase® Reporter system (HiBiT NanoDLR™) (Figure 17E).

[0142] Figures 18A-18B illustrate pools of HEK293 / Fluc cells delivered with RNP / ssODN mixtures for CRISPR-mediated HiBiT knock-in using either nucleofection or modified PEI or PAMAM polymers. To exclude complications from cell death during the process, cell pools were grown for several days before measurement. After HiBiT knock-in at the N-terminus of Fluc, viability, Fluc expression, and HiBiT signal were measured using CellTiter-Fluor and HiBiT NanoDLR (Figure 18A). The large drop in Fluc / CTF ratio for nucleofected cells may indicate loss of expression caused by InDel mutations. As shown by the HiBiT / CTF ratio, RNP / ssODN delivery mediated by modified polymers resulted in not only higher normalized Fluc expression but also higher normalized HiBiT signal. Similarly, modified PEI polymers show higher normalized HiBiT signals compared to nucleofection following delivery of RNP / ssODN mixtures designed to knock-in HiBiT at the C-terminus of GAPDH (Figure 18B).

[0143] For other cell types, the extent of HiBiT insertion was measured using the Nano-Glo® HiBiT solubility assay, and viability was measured using either CellTiter-Fluor in the same wells, or CellTiter-Glo® reagent (Promega catalog no. G7570) in replicate wells.

[0144] Diagram 1A. High-throughput model system for measuring HiBiT knock-in and Fluc knock-out. [ka]

[0145] Diagram 1B. gRNA and ssODN design for HiBiT knock-in in HEK293 / CMV-Fluc stable cell line. [ka] [Table 8]

[0146] Example 6 Degradation of HiBiT-BRD4 by PROTAC To demonstrate that PEI delivers functional LgBiT into cells, a proteolysis assay was used. HiBiT-BRD4 HEK293 cells were plated at 10,000 cells / well in wells of a 96-well plate. After 24 hours, cells were transfected with a complex of PBI-7666-3 (10ug / ml) and LgBiT protein (200nM). The complex was prepared by incubating PEI with LgBiT in Opti-MEM reduced serum medium for 30 minutes at room temperature. Cells treated with 10% BacMam-LgBiT to transduce the CMV-LgBiT expression construct served as a control. After 21 hours, the cell medium was replaced with fresh medium containing NanoGlo® Endurazine substrate (Promega catalog number N2571) and incubated for 3 hours. Next, cells were treated with a titration of MZ1, a bromodomain BET inhibitor, to target BRD4 for degradation. The kinetics was performed for 24 hours using a Clariostar instrument. Figure 19A illustrates the percentage of degraded BRD4 plotted to show the similarity of response between the two delivery methods of BacMam and PEI. Figure 19B illustrates the percentage of degraded BRD4 after 24 hours of treatment with MZ1, which responded in a dose-dependent manner.

[0147] Example 7 Removal of extracellular LgBiT HiBiT-KRAS clones from four different cell backgrounds (HEK293, A549, H1299, or MiaPaCa-2) were plated at 10,000 cells / well in wells of a 96-well plate. After 24 hours, cells were transfected with a complex of PBI-7666-3 (5ug / ml) and LgBiT protein (200nM). The complex was prepared by incubating PEI with LgBiT in Opti-MEM reduced serum medium for 30 minutes at room temperature. Cells treated with 10% BacMam-LgBiT to transduce the CMV-LgBiT expression construct served as a control. Cells were treated with digitonin (50ug / mL) and LgBiT protein (200nM). To distinguish intracellular versus extracellular luminescence signals, four conditions were examined. "No exchange condition" is when cells are treated with LgBiT·7666-3 for either 4 or 24 hours and luminescence is measured at a given time without medium exchange. "Exchange condition" is when cells are exchanged with fresh medium after LgBiT delivery either in the absence or presence of DarkBiT (SEQ ID NO:6) (1uM). DarkBiT peptide, a cell-impermeable peptide, is required to inactivate extracellular LgBiT. "Wash condition" is when cells are washed once with fresh medium after LgBiT delivery and exchanged with fresh medium followed by luminescence measurement. Wash condition reflects intracellular measurement of NanoBiT. Exchange condition removes some, but not all, extracellular LgBiT and therefore luminescence signal was lower than no exchange condition but higher than wash condition. At the given times, cells were assayed using the NanoGlo® Live Cell Assay System (Promega Catalog No. N2011) and the CellTiter-Glo® 2.0 Assay (Promega Catalog No. G7570). Luminescence was measured on a GloMax® Discover. Results are shown in Figures 20A-20D.

[0148] The PEI-based system delivers functional LgBiT into cells. The intracellular signals obtained from the PEI method were similar between 4-hour and 24-hour incubation times, suggesting that the method requires a minimum of 4-hour incubation time to reach its saturation signal. In contrast, BacMam transduction delivers nucleic acids. After 4 hours of incubation, the signal derived from BacMam was much lower than that of the PEI method for each of the tested cell lines. After 24 hours of incubation, in the case of HEK293 cells, the signal was comparable between the PEI method and BacMam transduction. Of the other three cases, BacMam transduction was better than the modified PEI compound in delivering LgBiT.

[0149] It is understood that the above-described detailed description and accompanying examples are merely illustrative and should not be taken as limitations on the scope of the present disclosure, which is defined solely by the appended claims and their equivalents.

[0150] Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art, including but not limited to, with respect to the chemical structures, substituents, derivatives, intermediates, syntheses, compositions, formulations, or methods of use of the present disclosure, may be made without departing from the spirit and scope of the present disclosure.

[0151] The sequences provided below are incorporated herein by reference and are provided as part of the accompanying Sequence Listing and the Sequence Listing Statement.

[0152] WT OgLuc (SEQ ID NO: 1)

[0153] MTLADF

[0154] NanoLuc (SEQ ID NO:2)

[0155] MVFTLEDFVGDWRQTAGYNLDQVLEQGGVSSLFQNLGVSVTPIQRIVLSGENGLKIDIHVIIPYEGLSGDQMGQIEKIFKVVYPVDDHHFKVILHYGTLVIDGVTPNMIDYFGRPYEGIAVFDGKKITVTGTLWNGNKIIDERLINPDGSLFRVTINGVTGWRLCERILA

[0156] HiBiT (SEQ ID NO: 3)

[0157] VSGWRLFKKIS

[0158] LgBiT (SEQ ID NO: 4)

[0159] MVFTLEDFVGDWRQTAGYNLDQVLEQGGVSSLFQNLGVSVTPIQRIVLSGENGLKIDIHVIIPYEGLSGDQMGQIEKIFKVVYPVDDHHFKVILHYGTLVIDGVTPNMIDYFGRPYEGIAVFDGKKITVTGTLWNGNKIIDERLINPDGSLLFRVTIN

[0160] SmBiT (SEQ ID NO: 5)

[0161] VTGYRLFEEIL

[0162] DarkBiT (SEQ ID NO: 6)

[0163] VSGWALFKKIS

[0164] DarkBiT (SEQ ID NO: 7)

[0165] MVSGWALFKKIS

[0166] DarkBiT (SEQ ID NO: 8)

[0167] MGVTGWRLCERILA

[0168] LgTrip 3092 (SEQ ID NO: 9)

[0169] VFTLDDFVGDWEQTAAYNLDQVLEQGGVSSLLQNLAVSVTPIMRIVRSGENALKIDIHVIIPYEGLSADQMAQIEEVFKVVYPVDDHHFKVILPYGTLVIDGVTPNKLNYFGRPYEGIAVFDGKKITVTGTLWNGNKIIDERLITPD

[0170] LgTrip 3546 (SEQ ID NO: 10)

[0171] VFTLDDFVGDWEQTAAYNLDQVLEQGGVSSLLQNLAVSVTPIMRIVRSGENALKIDIHVIIPYEGLSADQMAQIEEVFKVVYPVDDHHFKVILPYGTLVIDGVTPNKLNYFGRPYEGIAVFDGKKITTTGTLWNGNKIIDERLITPD

[0172] LgTrip 2098 (SEQ ID NO: 11)

[0173] VFTLDDFVGDWEQTAAYNLDQVLEQGGVSSLLQNLAVSVTPIMRIVRSGENALKIDIHVIIPYEGLSADQMAQIEEVFKVVYPVDDHHFKVILPYGTLVIDGVTPNKLNYFGRPYEGIAVFDGKKITTTGTLWNGNKIIDERLITPD

[0174] SmTrip9 (SEQ ID NO: 12)

[0175] GSMLFRVTINS Yet another aspect of the present invention may be as follows. [1] A compound or a salt thereof, A polyethyleneimine polymer; and a plurality of substituents attached to amino groups of the polyethyleneimine polymer, each substituent independently having the formula (I): -X-(CH 2 ) n -Z (I)、 During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, 2, 3, 4, or 5; The compound or a salt thereof, wherein Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group. [2] The compound according to [1] above, or a salt thereof, wherein the polyethyleneimine polymer has a weight average molecular weight of about 500 Da to about 250,000 Da. [3] The compound according to [2] above, or a salt thereof, wherein the polyethyleneimine polymer has a weight average molecular weight of about 500 Da to about 2000 Da. [4] The compound according to [2] above, or a salt thereof, wherein the polyethyleneimine polymer has a weight average molecular weight of about 5,000 Da to about 250,000 Da. [5] The compound or salt thereof according to any one of the above [1] to [4], wherein the above polyethyleneimine polymer is a branched polyethyleneimine polymer. [6] The compound or salt thereof according to any one of the above [1] to [4], wherein the polyethyleneimine polymer is a linear polyethyleneimine polymer. [7] Z is the following formula: -(CF 2 ) m -CF 3 wherein m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, or a salt thereof. [8] The compound or salt thereof according to any one of the above [1] to [6], wherein Z is a pentafluorophenyl group. [9] The compound or salt thereof according to any one of the above [1] to [6], wherein Z is an unsubstituted pyridyl group.

[10] X is -C(O)O-, n is 1 or 2; The compound according to any one of the above [1] to [9], or a salt thereof.

[11] Z is a group represented by the following formula: -(CF 2 ) m -CF 3 wherein m is 1, 2, 3, 4, or 5, or a salt thereof.

[12] X is a bond; n is 1 or 2; The compound according to any one of the above [1] to [9], or a salt thereof.

[13] The compound according to any one of [1] to

[12] above, wherein about 0.1 mol % to about 60 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I), or a salt thereof.

[14] The compound according to

[13] above, or a salt thereof, wherein about 5 mol % to about 50 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I).

[15] The compound according to

[14] above, or a salt thereof, wherein about 8 mol % to about 40 mol % of the amino groups of the polyethyleneimine polymer are bonded to a substituent of formula (I).

[16] A compound or a salt thereof, a poly(amidoamine) dendrimer; and a plurality of substituents attached to amino groups of the poly(amidoamine) dendrimer, each substituent independently having the formula (I): -X-(CH 2 ) n -Z (I)、 During the ceremony, X is a bond or -C(O)-O-; n is 0, 1, or 2; The compound or a salt thereof, wherein Z is selected from a haloalkyl group, an aryl group, a substituted aryl group, a heteroaryl group, and a substituted heteroaryl group.

[17] The compound according to

[16] above, or a salt thereof, wherein the poly(amidoamine) dendrimer is a first, second, third, fourth, fifth, sixth, seventh, eighth, ninth, or tenth generation poly(amidoamine) dendrimer.

[18] The compound according to

[17] above, or a salt thereof, wherein the poly(amidoamine) dendrimer is a first-generation, second-generation, third-generation, or fourth-generation poly(amidoamine) dendrimer.

[19] Z is a group represented by the following formula: -(CF 2 ) m -CF 3 wherein m is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10, or a salt thereof.

[20] The compound or salt thereof according to any one of the above

[16] to

[19] , wherein Z is a pentafluorophenyl group.

[21] The compound or salt thereof according to any one of the above

[16] to

[19] , wherein Z is an unsubstituted pyridyl group.

[22] The compound or salt thereof according to any one of the above

[16] to

[21] , wherein X is -C(O)O-.

[23] Z is a group represented by the following formula: -(CF 2 ) m -CF 3 wherein m is 1, 2, 3, 4, or 5, or a salt thereof.

[24] X is a bond; n is 1, The compound according to any one of the above

[16] to

[23] , or a salt thereof.

[25] The compound according to any one of

[16] to

[24] above, wherein about 0.1 mol % to about 80 mol % of primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I), or a salt thereof.

[26] The compound according to

[25] above, wherein about 10 mol % to about 70 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I).

[27] The compound according to

[26] above, wherein about 20 mol % to about 70 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I).

[28] A method for delivering a biomolecule to a cell, comprising: contacting the cell with an effective amount of the compound according to any one of [1] to

[27] above or a salt thereof; contacting the cell with the biomolecule; The method comprising:

[29] The method according to

[28] above, wherein the method comprises contacting the cell with an effective amount of two or more different compounds according to any one of [1] to

[27] above, or salts thereof.

[30] The method according to

[28] or

[29] , wherein the biological molecule is at least one of a deoxyribonucleic acid (DNA) molecule, a ribonucleic acid (RNA) molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof.

[31] The method according to

[28] or

[29] , wherein the biological molecule is a deoxyribonucleic acid (DNA) molecule or a ribonucleic acid (RNA) molecule.

[32] The method according to

[28] or

[29] , wherein the biomolecule is a peptide or polypeptide capable of luminescence.

[33] The method according to

[28] or

[29] , wherein the biological molecule comprises the polypeptide sequence of SEQ ID NO:4.

[34] The method according to

[28] or

[29] , wherein the biological molecule is a ribonucleoprotein complex containing a Cas9 protein.

[35] The method according to

[34] , wherein the ribonucleoprotein complex further comprises a guide RNA (gRNA) and a donor DNA template, the donor DNA template comprising a sequence encoding a polypeptide from SEQ ID NO:3.

[36] The method according to any one of

[28] to

[35] above, comprising mixing the compound and the biomolecule to form a mixture, and then contacting the cell with the mixture.

[37] A kit comprising the compound according to any one of [1] to

[27] above or a salt thereof.

[38] The kit according to

[37] , wherein the kit contains the compound or the salt thereof in a container.

[39] The kit according to

[37] or

[38] , further comprising at least one of a DNA molecule, an RNA molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof.

[40] The kit according to

[39] , wherein the peptide comprises a Cas9 protein.

[41] The kit described in

[39] , wherein the DNA molecule is a donor DNA template comprising a sequence encoding a polypeptide from SEQ ID NO:3.

[42] The kit according to any one of

[37] to

[41] above, further comprising instructions for using the compound or the salt thereof for transfection of a biological molecule.

[43] A method for modifying a sequence of an endogenous protein in a cell, the method comprising: Assembling a ribonucleoprotein (RNP) complex containing the Cas9 protein, a donor DNA template, and a guide RNA; delivering the RNP complex into a cell using the compound according to any one of [1] to

[27] above; The method comprising:

[44] A method for tagging an endogenous protein in a cell, the method comprising: assembling a ribonucleoprotein (RNP) complex comprising a Cas9 protein, a donor DNA template, and a guide RNA, the donor DNA template comprising a sequence encoding a peptide or polypeptide tag sequence; delivering the RNP complex into a cell using the compound according to any one of [1] to

[27] above; The method comprising:

[45] The method according to

[44] , wherein the donor DNA template comprises a sequence encoding a peptide tag selected from SEQ ID NO: 3 and SEQ ID NO: 5.

[46] The method of

[44] , wherein the donor DNA template further comprises homology arms flanking the sequence encoding a peptide or polypeptide tag sequence.

Claims

1. A compound or a salt thereof, the compound comprising: a third generation poly(amidoamine) dendrimer; and a plurality of substituents attached to amino groups of the poly(amidoamine) dendrimer, each substituent independently having the formula (I): -X-(CH 2 ) n -Z (I), During the ceremony, X is —C(O)—O—, n is 2; Z is a group represented by the following formula: The compound or a salt thereof, which is a haloalkyl group having --(CF 2 ) m --CF 3 , wherein m is 1, 2, 3, 4 or 5.

2. The compound of claim 1, or a salt thereof, wherein m is 2.

3. 3. The compound according to claim 1 or 2, wherein 0.1 mol % to 80 mol % of the primary amino groups of the poly(amidoamine) dendrimer are bonded to a substituent of formula (I), or a salt thereof.

4. 1. A method for delivering a biomolecule to a cell, comprising: contacting the cell with an effective amount of a compound according to claim 1 or 2, or a salt thereof; contacting the cell with the biomolecule; The method comprising:

5. 5. The method of claim 4, wherein the method comprises contacting the cells with an effective amount of two or more different compounds according to claim 1 or 2, or salts thereof.

6. The method of claim 4 , wherein the biological molecule is a deoxyribonucleic acid (DNA) molecule or a ribonucleic acid (RNA) molecule.

7. 7. The method of any one of claims 4 to 6, comprising mixing the compound and the biomolecule to form a mixture, and then contacting the cell with the mixture.

8. A kit comprising a compound according to claim 1 or 2, or a salt thereof.

9. The kit of claim 8 , wherein the kit comprises the compound or the salt thereof in a container.

10. 10. The kit of claim 8 or 9, further comprising at least one of a DNA molecule, an RNA molecule, a peptide, a polypeptide, a protein, or any combination or derivative thereof.

11. The kit according to any one of claims 8 to 10, further comprising instructions for using said compound or said salt thereof for transfection of a biomolecule.

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