Polypeptide conjugates for intracellular delivery of stapled peptides - Patent Application 20070122999

Abstract

The present disclosure provides novel polypeptide conjugates. The polypeptide conjugates disclosed herein comprise a stapled peptide, which comprises a peptide and at least one staple that holds the peptide in an α-helical structure, and a cyclic cell-penetrating peptide (cCPP) conjugated directly or indirectly to the stapled peptide. The present disclosure demonstrates that the cCPP can be used to confer consistent cell permeability to the stapled peptide.

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 62 / 578,213, filed October 27, 2017, the entire contents of which are incorporated herein by reference.

[0002] Government Funding Statement This invention was made with government support under Grant Nos. R01-GM110208 and R35-GM122459, each awarded by the National Institute of General Medical Sciences (NIGMS), National Institutes of Health (NIH). The government has certain rights in this invention. [Background technology]

[0003] background Stapled peptides have emerged as an exciting class of therapeutics for targeting intracellular protein-protein interactions (PPIs), challenging traditional targets for small molecules and biologics (Verdine GL, et al., Methods Enzymol. 503, 3-33 (2012); Walensky LD, et al., J. Med. Chem. 57, 6275-6288 (2014)). They recapitulate the structure and specificity of bioactive α-helices, resist proteolysis in vivo, and, when properly designed, access the cytosol and nucleus of mammalian cells. The initial cellular application of hydrocarbon-stapled α-helices, modeled after the BCL-2 homology 3 (BH3) domain of the proapoptotic protein BID, revealed their ability to be internalized intracellularly by an energy-dependent macropinocytosis mechanism, activating the apoptotic signaling cascade. Chu, Q., et al.,Med.Chem.Commun.6,111-119(2015)(clinicaltrials.gov identifier:NCT02264613).

[0004] Despite the remarkable promise of stapled peptides as a novel class of therapeutics for targeting previously intractable proteins, significant challenges remain in designing stapled peptides with consistent cell permeability. Many factors, including α-helicity, positive charge, peptide sequence, and staple composition and placement, appear to influence cellular uptake propensity. Recently, a comprehensive analysis of hundreds of stapled peptides in the Verdine and Walensky laboratories demonstrated that optimal hydrophobicity, positive charge, and helical content, along with proper staple placement, are key drivers of cellular uptake, whereas excessive hydrophobicity and positive charge can trigger membrane lysis at increased peptide doses. (See Chu, Q., et al., Med. Chem. Commun. 6, 111-119 (2015); Nature Chemical Biology. 12, 845-852 (2016)). These studies reveal that many stapled peptides are impermeable or poorly permeable to cell membranes, limiting their applicability as therapeutic agents.

[0005] Therefore, there is a need in the art for improved stapled peptides with enhanced cell permeability. Summary of the Invention

[0006] This disclosure provides polypeptide conjugates for intracellular delivery of stapled peptides. This disclosure demonstrates that cyclic cell-penetrating peptides (cCPPs) can be used to confer consistent cell permeability to stapled peptides. In addition, two methods are provided for stapling α-helical peptides and conjugating them to cCPPs.

[0007] In embodiments, the present disclosure provides polypeptide conjugates comprising a stapled peptide comprising a peptide and at least one staple holding the peptide in an α-helical conformation, and at least one cyclic cell-penetrating peptide (cCPP) conjugated, directly or indirectly, to the stapled peptide. In embodiments, the cCPP of the present disclosure is conjugated, directly or indirectly, to the staple. In further embodiments, the cCPP is conjugated, directly or indirectly, to the peptide. In still further embodiments, the cCPP is conjugated, directly or indirectly, to the N-terminus of the peptide. In other embodiments, the cCPP is conjugated, directly or indirectly, to the C-terminus of the peptide. In further embodiments, the cCPP is conjugated, directly or indirectly, to the side chain of an amino acid of the peptide. In the polypeptide conjugates of the present disclosure, the staple may be selected from the group consisting of amide, alkylene, N-alkylene, alkenylene, alkynylene, aryl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, and heteroaryl, each of which is optionally substituted.

[0008] The polypeptide conjugates of the present invention may further comprise a linker covalently bonded to an amino acid on the cCPP and either an amino acid on the peptide or the staple. In some embodiments, the linker is covalently bonded to the staple peptide via a disulfide bond. In further embodiments, the linker is selected from the group consisting of at least one amino acid, alkylene, alkenylene, alkynylene, aryl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, heteroaryl, ether, and combinations thereof, each of which may be optionally substituted. In embodiments, the linker is capable of releasing the staple peptide from the cCPP after the polypeptide conjugate enters the cytosol of a cell.

[0009] The polypeptide conjugates of the invention may be represented by formula IA, IB, or IC: [ka] During the ceremony, each of X and Z, at each occurrence, is independently selected from an amino acid; U, in each occurrence and if present, is independently selected from amino acids; J, in each occurrence and if present, is independently selected from an amino acid; Z', in each occurrence and presence, is independently selected from an amino acid; a is a number ranging from 0 to 500; c is at least 3; d is a number ranging from 1 to 500; e is a number ranging from 0 to 500; each of g and h is independently 0 or 1 in each occurrence, provided that g is 1 in at least one occurrence; i is a number ranging from 0 to 100; Y1 is an amino acid having a side chain that forms a first binding group (b1) to the staple, and Y2 is an amino acid having a side chain that forms a second binding group (b2) to the staple; The structure may be as follows:

[0010] In some embodiments, c is a number ranging from 3 to 30. In some embodiments, c is 3, 6, or 10. In further embodiments, each of b1 and b2 is independently selected from a bond, an aryl, a thioether, a disulfide, an amide, an ester, and an ether.

[0011] In embodiments, J is absent, and Z may be at either the N- or C-terminus of the peptide. In embodiments, J is present, e is 1, and J may be at either the N- or C-terminus of the peptide. In further embodiments, J is present, e is 2 or greater, and terminal J may be at either the N- or C-terminus of the peptide. In other embodiments, U is absent, and Z' is at either the N- or C-terminus of the peptide. In embodiments, U is present, a is 1, and U is at either the N- or C-terminus of the peptide. In embodiments, U is present, a is 2 or greater, and U is at either the N- or C-terminus of the peptide.

[0012] In embodiments, the polypeptide conjugate of formula IB may have the following structure: [ka]

[0013] In embodiments, the polypeptide conjugate of formula IC may have the following structure: [ka]

[0014] In embodiments, the cCPP has formula II: [ka] During the ceremony, each of AAl, AA2, AA3, and AA4 is independently selected from a D-amino acid or an L-amino acid; AA u and A.A. z is independently selected from a D-amino acid or an L-amino acid in each occurrence and when present; m and n are independently selected from the numbers 0 to 6; During the ceremony, AAU, in each case and if present, AA u , AA1, AA2, AA3, AA4, and AAz wherein at least two amino acids selected from the group consisting of: AA u , in each case and if present, AA1, AA2, AA3, AA4, and AA z wherein at least two amino acids selected from the group consisting of: are independently in each occurrence and when present, hydrophobic amino acids; It may have a sequence comprising:

[0015] In some embodiments, the cCPP has the formula IIIA-D: [ka] During the ceremony, AA H1 and A.A. H2 each of which is independently a D hydrophobic amino acid or an L hydrophobic amino acid; In each case and if present, AA U and A.A. Z are each independently a D-amino acid or an L-amino acid; m and n are independently selected from the numbers 0 to 6; The sequence may include any of the following:

[0016] The present disclosure also provides cells comprising the polypeptide conjugates disclosed herein.

[0017] The present disclosure further provides a method for cellular delivery of a stapled peptide, the method comprising contacting a cell with a polypeptide conjugate disclosed herein.

[0018] The present disclosure further provides a method for treating a patient in need thereof, the method comprising administering to the patient a polypeptide conjugate disclosed herein. The patient may have a disease or condition selected from cancer, an inflammatory disease or condition, and an autoimmune disease or condition.

[0019] Additionally, the present disclosure provides methods for making the polypeptide conjugates disclosed herein, the methods comprising conjugating a stapled peptide and a cCPP. In other embodiments, the present disclosure provides methods for making the polypeptide conjugates disclosed herein, the methods comprising conjugating a peptide to at least one cCPP and stapling the peptide.

[0020] The present disclosure also provides pharmaceutical compositions comprising the peptide conjugates disclosed herein. [Brief explanation of the drawings]

[0021] [Figure 1] FIG. 1 is a schematic diagram showing the strategy for synthesizing cCPP-staple peptides conjugated with DCA as the staple.

[0022] [Figure 2] Figure 2 shows survival curves showing the effects of staple peptide 2 (3-1-1-DCA), CPP9-staple peptide conjugates 4 and 5 (3-1-1-DCA-CP9 peak 1 and peak 2), and nutlin-3 on the viability of wild-type p53 cell lines (HCT116 WT) and p53 knockout cell lines (HCT116 p53- / -).

[0023] [Figure 3A-3B] Figures 3A-3B are schematic diagrams showing two different strategies for synthesizing cCPP-stapled peptides conjugated with BBA as a staple / linker. Figure 3A shows an on-resin stapling strategy, in which the helical peptide, BBA staple / linker, and cCPP are synthesized sequentially on resin. Figure 3B shows a solution-phase stapling strategy, in which the BBA-derivatized cCPP and helical peptide are synthesized separately and then stapled / conjugated in solution.

[0024] [Figure 4]Figure 4 shows a comparison of the whole-cell efficiency of stapled peptides with and without CPP9 conjugation. HeLa cells were treated with 5 μM FITC-labeled peptide for 2 h at 37°C, washed to remove excess peptide, and then subjected to confocal microscopy on live cells. I, DIC; II, GFP channel; and III, overlap of I and II.

[0025] [Figure 5] FIG. 5 shows the chemical structures of unstapled peptides 4 and 5 (stereoisomers), HPLC chromatograms, and low-resolution MALDI-TOF MS spectra of the products (retention time=32 min).

[0026] [Figure 6] Figure 6 shows the chemical structure of stapled peptide 3, the HPLC chromatogram, and the low-resolution MALDI-TOF MS spectrum of the product (retention time = 30.5 min).

[0027] [Figure 7] FIG. 7 shows the chemical structure of aminooxy-cCPP9, an HPLC chromatogram, and a low-resolution MALDI-TOF MS spectrum of aminooxy-cCPP9 (retention time=22 min).

[0028] [Figure 8A] Figure 8A shows the chemical structures of stapled peptides 4 and 5 (stereoisomers) conjugated to cCPP (cCPP 9) via a linker and HPLC chromatograms. Figure 8B shows low-resolution MALDI-TOF MS spectra of aminooxy cCPP 9 (peak retention time = 23 min), Structure 4 (peak retention time = 33.5 min), and Structure 5 (peak retention time = 34.5 min).

[0029] [Figure 9] FIG. 9 shows the chemical structure, HPLC chromatogram, and MS spectrum of stapled, labeled peptide 10.

[0030] [Figures 10A-10B] 10A-10B show the chemical structure, HPLC chromatogram (FIG. 10A), and MS spectrum (FIG. 10B) of stapled, labeled peptide 11 conjugated to cCPP via a linker.

[0031] [Figure 11A-1B] 11A-1B show the chemical structure, HPLC chromatogram (FIG. 11A), and MS spectrum (FIG. 11B) of stapled, labeled peptide 12.

[0032] [Figures 12A-12B] 12A-12B show the chemical structure, HPLC chromatogram (FIG. 12A), and MS spectrum (FIG. 12B) of stapled, labeled peptide 13 conjugated to cCPP via a linker.

[0033] [Figure 13] FIG. 13 shows the chemical structure, HPLC chromatogram, and MS spectrum of stapled, labeled peptide 14.

[0034] [Figures 14A-14B] 14A-14B show the chemical structure, HPLC chromatogram (FIG. 14A), and MS spectrum (FIG. 14B) of stapled, labeled peptide 15 conjugated to cCPP via a linker.

[0035] [Figure 15] FIG. 15 shows the chemical structure, HPLC chromatogram, and MS spectrum of stapled, labeled peptide 16.

[0036] [Figures 16A-16B] 16A-16B show the chemical structure, HPLC chromatogram (FIG. 16A), and MS spectrum (FIG. 16B) of stapled, labeled peptide 17 conjugated to cCPP via a linker.

[0037] [Figure 17] FIG. 17 shows the chemical structure, HPLC chromatogram, and MS spectrum of stapled, labeled peptide 18.

[0038] [Figures 18A-18B] Figures 18A-18B show the chemical structure, HPLC chromatogram (Figure 18A), and MS spectrum (Figure 18B) of stapled, labeled peptide 19 conjugated to cCPP via a linker.

[0039] [Figure 19] FIG. 19 shows the chemical structure, HPLC chromatogram, and MS spectrum of stapled, labeled peptide 21 conjugated to a cCPP via a linker.

[0040] [Figures 20A-20D] Figures 20A-20D show the chemical structures of amide-stapled peptides and conjugates, including sPDI peptide 22 (Figure 20A), CPP9-sPDI peptide conjugate 23 (Figure 20B), R9-sPDI peptide conjugate 24 (Figure 20C), and Tat-sPDI peptide conjugate 25 (Figure 20D). CPP9, R9, and Tat are each conjugated to the peptide via a linker attached to their C-terminus.

[0041] [Figure 21] Figure 21 shows a comparison of the whole cell efficacy of stapled peptides with and without conjugation. Images were provided for Structure 22 (sPDI), Structure 23 (CPP9-sPDI), Structure 24 (R9-sPDI), and Structure 25 (Tat-sPDI). Analogs bearing Lys(FITC) at the N-terminus were used for confocal imaging analysis.

[0042] [Figure 22]Figure 22 shows a graph of a cell-free competition experiment comparing the functional cytosolic delivery of sPDI (Structure 22), CPP9-sPDI (Structure 23), and the CPP9-sPDI F10A mutant. Fluorescence polarization (FP) plots were obtained using FITC-labeled MDM2 ligand (15 nM) in the presence of MDM2 (15 nM) and unlabeled sPDI, CPP9-conjugated stapled PDI (CPP9-sPDI; Structure 23), or the CPP9-sPDI F10A mutant (0-5 μM) as a function of competitor peptide concentration.

[0043] [Figure 23] Figure 23 shows a graph of an antiproliferative assay comparing the effect of 72 hour treatment with CPP9-sPDI (Structure 23), Nutlin-3a, R9-sPDI (Structure 24), sPDI (Structure 22), CPP9-sPDI(F10A), and Tat-sPDI (Structure 25, 0-20 μM) on the viability of the SJSA-1 cell line in the presence of 10% FBS as measured by MTT assay. IC50 values ​​(M) are provided for each test compound.

[0044] [Figure 24] Figure 24 is a graph showing that the antiproliferative activity of CPP9-sPDI (Structure 23) is mediated by the apoptotic pathway. After 48 hours of treatment with the inhibitor in the presence of 10% FBS, the percentage of Annexin V / PI and Annexin V / PI SJSA-1 cells was measured.

[0045] [Figure 25] FIG. 25 is a graph showing the stability of CPP9-sPDI (structure 23) in 25% human serum at 37° C. DETAILED DESCRIPTION OF THE INVENTION

[0046] When describing the present invention, all terms not defined herein have their general meaning recognized in the art. Terms or expressions not expressly defined herein shall have their generally accepted definitions as understood by those skilled in the art. To the extent that the following description relates to a particular embodiment or particular use of the present invention, it is for illustrative purposes only and does not limit the claimed invention. The following description is intended to cover all alternatives, modifications, and equivalents that are included within the spirit and scope of the present invention, as defined by the appended claims.

[0047] definition As used herein, "amino acid" refers to a moiety present in the staple peptide conjugate of the present disclosure. As used herein, "hydrophobic amino acid" refers to an amino acid having a hydrophobic group (e.g., an alkyl chain) in its side chain. Similarly, "aromatic amino acid" refers to an amino acid having an aromatic group (e.g., phenyl) in its side chain.

[0048] "Alkylene" or "alkylene chain" means a fully saturated, straight or branched divalent hydrocarbon chain radical having from 1 to 40 carbon atoms. 40 Non-limiting examples of alkylene include ethylene, propylene, n-butylene, ethenylene, propenylene, n-butenylene, propynylene, n-butynylene, etc. In some embodiments, the alkylene chain is directly or indirectly attached to the cCPP via a single bond and directly or indirectly attached to the staple or peptide via a single bond. In some embodiments, the alkylene chain is independently attached, directly or indirectly, to the side chains of the first amino acid of the peptide and the second amino acid of the peptide. Unless otherwise specified herein, the alkylene chain may be optionally substituted as described herein.

[0049] "Alkenylene" or "alkenylene chain" means a straight or branched divalent hydrocarbon chain radical having 2 to 40 carbon atoms and one or more carbon-carbon double bonds. 40 Non-limiting examples of alkenylene include ethene, propene, butene, etc. In some embodiments, the alkenylene chain is directly or indirectly attached to the cCPP via a single bond and directly or indirectly attached to the staple or peptide via a single bond. In some embodiments, the alkenylene chain is independently attached, directly or indirectly, to the side chains of the first amino acid of the peptide and the second amino acid of the peptide. Unless otherwise specified herein, the alkenylene chain may be optionally substituted.

[0050] "Alkynylene" or "alkynylene chain" means a straight or branched divalent hydrocarbon chain radical having 2 to 40 carbon atoms and one or more carbon-carbon triple bonds. 40 Non-limiting examples of alkynylene include ethynylene, propargylene, etc. In some embodiments, the alkynylene chain is directly or indirectly attached to the cCPP via a single bond, and directly or indirectly attached to the staple or peptide via a single bond. In some embodiments, the alkynylene chain is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and directly or indirectly to the side chain of the second amino acid of the peptide. Unless otherwise specified herein, the alkynylene chain may be optionally substituted.

[0051] "Aryl" refers to a hydrocarbon ring structure divalent radical containing hydrogen, 6 to 40 carbon atoms, and at least one aromatic ring. For purposes of this invention, an aryl divalent radical can be a monocyclic, bicyclic, tricyclic, or tetracyclic ring structure, which may include fused or bridged ring structures. Aryl divalent radicals include, but are not limited to, aryl divalent radicals derived from aceanthrylene, acenaphthylene, acephenanthrylene, anthracene, azulene, benzene, chrysene, fluoranthene, fluorene, as-indacene, s-indacene, indane, indene, naphthalene, phenalene, phenanthrene, pleiadene, pyrene, and triphenylene. In some embodiments, the aryl divalent radical is attached directly or indirectly to a cCPP via a single bond and to a staple or peptide via a single bond. In some embodiments, the aryl is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and, directly or indirectly, to either the staple or the side chain of the second amino acid of the peptide. Unless otherwise specified herein, the aryl may be optionally substituted.

[0052] "Cycloalkyl" refers to a stable, non-aromatic, monocyclic or polycyclic, fully saturated hydrocarbon divalent radical having 3 to 40 carbon atoms and at least one ring, where the ring is composed solely of carbon and hydrogen atoms and may include fused or bridged ring structures. Monocyclic cycloalkyl divalent radicals include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl. Polycyclic cycloalkyl divalent radicals include, for example, adamantyl, norbornyl, decalinyl, 7,7-dimethyl-bicyclo[2.2.1]heptanyl, and the like. In some embodiments, the cycloalkyl divalent radical is attached, directly or indirectly, via a single bond to a cCPP and, directly or indirectly, via a single bond to a staple or peptide. In some embodiments, the cycloalkyl is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and, directly or indirectly, to either the side chain of the second amino acid of the staple or peptide. Unless stated otherwise in the specification, a cycloalkyl group may be optionally substituted.

[0053] "Cycloalkenyl" refers to a stable, non-aromatic, monocyclic or polycyclic, fully saturated hydrocarbon divalent radical having 3 to 40 carbon atoms and at least one ring containing one or more carbon-carbon double bonds, wherein the ring is composed solely of carbon and hydrogen atoms and may include fused or bridged ring structures. Monocyclic cycloalkenyl radicals include, for example, cyclopentenyl, cyclohexenyl, cycloheptenyl, and cycloctenyl. Polycyclic cycloalkenyl radicals include, for example, bicyclo[2.2.1]hept-2-enyl. In some embodiments, the cycloalkenyl divalent radical is attached, directly or indirectly, via a single bond to a cCPP and, directly or indirectly, via a single bond to a staple or peptide. In some embodiments, the cycloalkenyl is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and, directly or indirectly, to either the side chain of the second amino acid of the staple or peptide. Unless stated otherwise in the specification, a cycloalkenyl group may be optionally substituted.

[0054] "Cycloalkynyl" refers to a stable, non-aromatic, monocyclic or polycyclic, fully saturated hydrocarbon divalent radical having 3 to 40 carbon atoms and at least one ring containing one or more carbon-carbon triple bonds, wherein the ring is composed solely of carbon and hydrogen atoms and may include fused or bridged ring structures. Monocyclic cycloalkynyl radicals include, for example, cycloheptynyl and cyclooctynyl. In some embodiments, the cycloalkynyl divalent radical is attached, directly or indirectly, via a single bond to a cCPP and, directly or indirectly, via a single bond to a staple or peptide. In some embodiments, the cycloalkynyl is independently attached, directly or indirectly, to the side chain of the first amino acid in the peptide and, directly or indirectly, to either the side chain of the second amino acid in the staple or peptide. Unless otherwise specified herein, a cycloalkynyl group may be optionally substituted.

[0055] "Heterocyclyl," "heterocyclic ring," or "heterocycl" refers to a stable 3- to 20-membered aromatic or non-aromatic divalent radical, consisting of 2 to 12 carbon atoms and 1 to 6 heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur. Heterocyclyl or heterocyclic rings include heteroaryl, as defined below. Unless specifically stated otherwise in the specification, a heterocyclyl radical can be a monocyclic, bicyclic, tricyclic, or tetracyclic ring structure, which can include fused or bridged ring structures. In addition, the nitrogen, carbon, or sulfur atoms in the heterocyclyl radical can be optionally quaternized. In addition, the heterocyclyl radical can be partially or fully saturated. Examples of such heterocyclyl radicals include, but are not limited to, dioxolanyl, thienyl[1,3]dithianyl, decahydroisoquinolyl, imidazolinyl, imidazolidinyl, isothiazolidinyl, isoxazolidinyl, morpholinyl, octahydroindolyl, octahydroisoindolyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolidinyl, oxazolidinyl, piperidinyl, piperazinyl, 4-piperidonyl, pyrrolidinyl, pyrazolidinyl, quinuclidinyl, thiazolidinyl, tetrahydrofuryl, trithianyl, tetrahydropyranyl, thiomorpholinyl, thiamorpholinyl, 1-oxo-thionorpholinyl, and 1,1-dioxo-thiomorpholinyl. In some embodiments, the heterocyclyl divalent radical is directly or indirectly attached to the cCPP via a single bond and directly or indirectly attached to the staple or peptide via a single bond. In some embodiments, the heterocyclyl is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and, directly or indirectly, to either the side chain of the second amino acid of the staple or peptide. Unless otherwise specified herein, the heterocyclyl group may be optionally substituted.

[0056] "Heteroaryl" refers to a 5- to 20-membered ring system radical containing a hydrogen atom, 1 to 13 carbon atoms, 1 to 6 heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and at least one aromatic ring. For purposes of this invention, a heteroaryl radical can be a monocyclic, bicyclic, tricyclic, or tetracyclic ring structure, which can include fused or bridged ring structures. Additionally, the nitrogen, carbon, or sulfur atoms in the heteroaryl radical can be optionally quaternized. Examples include azepinyl, acridinyl, benzimidazolyl, benzothiazolyl, benzindolyl, benzodioxolyl, benzofuranyl, benzoxazolyl, benzothiazolyl, benzothiadiazolyl, benzo[b][1,4]dioxepinyl, 1,4-benzodioxanyl, benzonaphthofuranyl, benzoxazolyl, benzodioxolyl, benzodioxinyl, benzopyranyl, benzopyranonyl, benzofuranyl, benzofuranonyl, benzothienyl (benzothiophenyl), benzotriazolyl, benzo[4,6]imidazo[1,2-a]pyridinyl, carbazolyl, cinnolinyl, dibenzofuranyl, dibenzothiophenyl, furanyl, furanonyl, isothiazolyl, imidazolyl, indazolyl, indolyl, indazolyl, isoindolyl, indophenyl, and indophenyl. Examples of aryl groups include, but are not limited to, dolinyl, isoindolinyl, isoquinolyl, indolizinyl, isoxazolyl, naphthyridinyl, oxadiazolyl, 2-oxoazepinyl, oxazolyl, oxiranyl, 1-oxidopyridinyl, 1-oxidopyrimidinyl, 1-oxidopyrazinyl, 1-oxidopyridazinyl, 1-phenyl-1H-pyrrolyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pteridinyl, purinyl, pyrrolyl, pyrazolyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, quinazolinyl, quinoxalinyl, quinolinyl, quinuclidinyl, isoquinolinyl, tetrahydroquinolinyl, thiazolyl, thiadiazolyl, triazolyl, tetrazolyl, triazinyl, and thiophenyl (i.e., thienyl).In some embodiments, the heteroaryl divalent radical is directly or indirectly attached to the cCPP via a single bond and directly or indirectly attached to the staple or peptide via a single bond. In some embodiments, the heteroaryl is independently attached, directly or indirectly, to the side chain of the first amino acid of the peptide and directly or indirectly to the side chain of the second amino acid of the staple or peptide. Unless otherwise specified herein, the heteroaryl group may be optionally substituted.

[0057] As used herein, the term "ether" refers to a group of the formula -[(R1) m -O-(R2) n ] z -, wherein each of m, n, and z is independently selected from 1 to 40, and each of R1 and R2 is independently an alkylene, alkenylene, alkynylene, aryl, heteroaryl, cycloalkyl, cycloalkenyl, cycloalkynyl, or heterocyclyl group. In some embodiments, each of R1 and R2 is independently a straight-chain or branched alkylene group. In certain embodiments, an ether has the formula -[(CH2) m -O-(CH2) n ] z wherein m, n, and z are each independently selected from 1 to 40. Examples include polyethylene glycol. The ether is attached to the cCPP directly or indirectly via a single bond and is attached to the staple or peptide directly or indirectly via a single bond. Unless otherwise specified herein, the ether may be optionally substituted.

[0058] As used herein, the term "N-alkylene" means an alkylene divalent radical, as defined above, containing at least one nitrogen atom, and the point of attachment of the alkylene radical to the remainder of the molecule is through the alkylene radical. In some embodiments, the point of attachment can optionally be the nitrogen atom. Unless otherwise specified in the specification, an N-alkylene group can be optionally substituted.

[0059] As used herein, "peptide" or "polypeptide" includes a polymer of amino acid residues linked together by peptide (amide) bonds. The term, as used herein, refers to proteins, polypeptides, and peptides of any size, structure, or function. Typically, a peptide or polypeptide will be at least three amino acids long. A peptide or polypeptide may refer to an individual protein or a collection of proteins. The peptides of the present invention may contain natural amino acids and / or unnatural amino acids (i.e., compounds that do not occur in nature but can be incorporated into a polypeptide chain). Amino acid analogs well known in the art may alternatively be used. One or more amino acids in a peptide or polypeptide may be modified by chemicals, such as the addition of carbohydrate groups, hydroxy groups, phosphate groups, farnesyl groups, isofarnesyl groups, fatty acid groups, or linkers for conjugation, functionalization, or other modifications. A peptide or polypeptide may also be a single molecule or a multimolecular complex, such as a protein. A peptide or polypeptide may be simply a fragment of a naturally occurring protein or peptide. A peptide or polypeptide may be naturally occurring, recombinant, synthetic, or any combination thereof.

[0060] "Stapling" or "peptide stapling" is a strategy for constraining peptides, typically in an α-helical structure. Stapling is achieved by covalently linking the side chains of two amino acids on a peptide, thereby forming a peptide macrocycle. Stapling generally involves introducing at least two moieties into a peptide that can undergo a reaction to generate at least one crosslinker between them. These moieties may be two amino acids with appropriate side chains introduced into the peptide sequence, or they may represent chemical modifications of the side chains. Stapling imposes constraints on secondary structures, such as α-helical structures. The length and shape of the crosslinker can be optimized to improve the yield of the desired secondary structure content. This imposed constraint can, for example, prevent the secondary structure from unfolding and / or reinforce the shape of the secondary structure. Secondary structures that are prevented from unfolding are, for example, more stable.

[0061] A "stapled peptide" is a peptide containing staples (as described in detail herein). More specifically, a stapled peptide is a peptide in which one or more amino acids on the peptide are cross-linked to hold the peptide in a particular secondary structure, e.g., an α-helical structure. A stapled peptide peptide contains a selected number of natural or unnatural amino acids and further contains at least two moieties that undergo a reaction to generate at least one cross-linker between the at least two moieties, thus, for example, modulating the stability of the peptide.

[0062] A "stitched" peptide is a stapled peptide that includes two or more (eg, 2, 3, 4, 5, 6, etc.) staples.

[0063] The term "substituted" as used herein refers to any of the above groups (i.e., alkylene, alkenylene, alkynylene, aryl, carbocyclyl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, heteroaryl, and / or ether) in which at least one hydrogen atom is replaced with at least one non-hydrogen atom, including, but not limited to, halogen atoms such as F, Cl, Br, and I; oxygen atoms such as hydroxyl, alkoxy, and ester groups; sulfur atoms in groups such as thiol, thioalkyl, sulfone, sulfonyl, and sulfoxide groups; nitrogen atoms in groups such as amine, amide, alkylamine, dialkylamine, arylamine, alkylarylamine, diarylamine, N-oxide, imide, and enamine; silicon atoms in groups such as trialkylsilyl, dialkylarylsilyl, alkyldiarylsilyl, and triarylsilyl groups; and heteroatoms in various other groups. "Substituted" also refers to any of the above groups in which one or more hydrogen atoms have been replaced by a higher bond (e.g., a double or triple bond) to a heteroatom, e.g., oxygen in oxo, carbonyl, carboxyl, and ester groups; and nitrogen in groups such as imine, oxime, hydrazone, and nitrile. For example, "substituted" refers to any group ... g R h , -NR g C(=O)R h , -NR g C(=O)NR g R h , -NR g C(=O)OR h , -NR g SO2R h , -OC(=O)NR g R h , -OR g , -SR g , -SOR g , -SO2R g , -OSO2R g , -SO2OR g , =NSO2R g, and -SO2NR g R h "Substituted" also includes any of the above groups in which one or more hydrogen atoms have been replaced with -C(=O)R. g , -C(=O)OR g , -C(=O)NR g R h , -CH2SO2R g , -CH2SO2NR g R h In the above, R g and R hare the same or different and independently hydrogen, alkyl, alkenyl, alkynyl, alkoxy, alkylamino, thioalkyl, aryl, aralkyl, cycloalkyl, cycloalkenyl, cycloalkynyl, cycloalkylalkyl, haloalkyl, haloalkenyl, haloalkynyl, heterocyclyl, N-heterocyclyl, heterocyclylalkyl, heteroaryl, N-heteroaryl, and / or heteroalkylalkyl. "Substituted" also means any of the above groups in which one or more hydrogen atoms are replaced by a bond to an amino, cyano, hydroxyl, imino, nitro, oxo, thioxo, halo, alkyl, alkenyl, alkynyl, alkoxy, alkylamino, thioalkyl, aryl, aralkyl, cycloalkyl, cycloalkenyl, cycloalkynyl, cycloalkylalkyl, haloalkyl, haloalkenyl, haloalkynyl, heterocyclyl, N-heterocyclyl, heterocyclylalkyl, heteroaryl, N-heteroaryl, and / or heteroarylalkyl group. In addition, each of the above substituents may also be optionally substituted with one or more of the above substituents. Furthermore, those skilled in the art will recognize that "substituted" also encompasses the moment one or more hydrogen atoms in any of the groups described herein are replaced with a functional group, and the moment the functional group reacts to form a covalent bond with a cCPP, staple, or peptide. The reaction product is also considered a substituent. For example, in embodiments in which a linker is attached to a staple, the staple may be appropriately substituted with a group capable of forming a bond to the linker. In some embodiments, the sample may be substituted with a carbonyl group (e.g., a ketone or aldehyde), which, upon coupling with a linker bearing a nucleophilic hydroxylamine, forms an oxime (e.g., Figure 1). In another example, any of the above groups may be substituted at the first position with a carboxylic acid (i.e., -C(=O)OH) that forms an amide bond with the appropriate amino acid CPP (e.g., lysine). Alternatively, or in addition, any of the above groups may be substituted with an electrophilic group (e.g., -C(=O)H, -COR) that forms a bond with the N-terminus of the peptide. g , -halides, etc., where Rg is a leaving group), or a nucleophilic group (-NH2, -NHR) that forms a bond with the C-terminus of the peptide. g , —OH, etc. In other embodiments, this group replaces a cysteine ​​(or an amino acid analogue having a thiol group) in the peptide with a thiol group that forms a disulfide bond.

[0064] The term "radical" as used herein with respect to the above groups refers to the electrons involved in forming the bond to the moiety to which it is attached. For example, when the polypeptide conjugates disclosed herein include an ether linker joining the cCCP to the staple peptide, either linker is defined as a divalent radical prior to conjugation. To form the polypeptide conjugate, one electron of the divalent radical is shared in a single bond to the cCCP, and the other electron is shared in a single bond with the staple peptide.

[0065] The term "indirectly," when used in conjunction with attached or conjugated, refers to a connection between groups (e.g., a cCPP and a staple peptide) that is achieved using a linker. For example, according to some embodiments, a cCPP can be indirectly attached to a staple using a linker.

[0066] Polypeptide Conjugates In various embodiments, the present disclosure provides polypeptide conjugates comprising a peptide and a staple peptide comprising at least one staple holding the peptide in an α-helical structure, and at least one cyclic cell-penetrating peptide (cCPP) conjugated, directly or indirectly, to the staple peptide. The cCPP can be conjugated to the staple peptide at any suitable position. In some embodiments, the cCPP may be conjugated, directly or indirectly, to the staple. In other embodiments, the cCPP can be conjugated, directly or indirectly, to the peptide at any suitable position, including the side chain of an amino acid in the peptide or the N-terminus or C-terminus of the peptide. Thus, in some embodiments, the cCPP can be conjugated, directly or indirectly, to the N-terminus of the peptide. In other embodiments, the cCPP can be conjugated, directly or indirectly, to the C-terminus of the peptide. In still other embodiments, the cCPP can be conjugated, directly or indirectly, to the side chain of an amino acid in the peptide.

[0067] The polypeptide conjugates of the invention may be represented by formula IA, IB, or IC: [ka] may have

[0068] In some embodiments, each of X and Z, at each occurrence, is independently selected from an amino acid. In some embodiments, U, at each occurrence and when present, is independently selected from an amino acid. In some embodiments, J, at each occurrence and when present, is independently selected from an amino acid. In some embodiments, Z', at each occurrence and when present, is independently selected from an amino acid.

[0069] In some embodiments, d is a number ranging from 1 to 500. In some embodiments, e is a number ranging from 0 to 500. In some embodiments, i is a number ranging from 0 to 100.

[0070] In some embodiments, each of g and h is independently 0 or 1 in each occurrence, provided that at least g is 1. Thus, in some embodiments, the peptide conjugate can include one cCPP-linker moiety (e.g., when d=1, g=1, and h=0 in Formula IB), or more than one cCPP-linker moiety (e.g., when d=2, g=2, and h=0 in Formula IB, or when d=10, g=2, and h=0 in Formula IB).

[0071] In some embodiments, a is a number ranging from 0 to 500. In some embodiments, c is at least 3. In some embodiments, c can be any number greater than or equal to 3, such that the staples (described herein) are on the same face of the alpha helix. In some embodiments, c is 3, 6, or 10. In further embodiments, each of b1 and b2 is selected from a bond, an aryl, a thioether, a disulfide, an amide, an ester, and an ether.

[0072] In some embodiments, Y1 is an amino acid having a side chain that forms a first linkage group (b1) to the staple, and Y2 is an amino acid having a side chain that forms a second linkage group (b2) to the staple.

[0073] The present disclosure contemplates that the structure of formula IA, IB, or IC may be interpreted as having an N to C or C to N orientation. That is, the top of the structure may be either the N-terminus or the C-terminus. Similarly, the bottom of the structure may be either the C-terminus or the N-terminus. In embodiments, J is absent, and Z may be either the N-terminus or the C-terminus of the peptide. In embodiments, it is present, e is 1, and J may be either the N-terminus or the C-terminus of the peptide. In further embodiments, J is present, e is 2 or greater, and the terminus J may be either the N-terminus or the C-terminus of the peptide. In other embodiments, U is absent, and Z' is either the N-terminus or the C-terminus of the peptide. In embodiments, U is present, a is 1, and U is either the N-terminus or the C-terminus of the peptide. In embodiments, U is present, a is 2 or greater, and U is either the N-terminus or the C-terminus of the peptide.

[0074] In embodiments, the polypeptide conjugate of formula IB may have the following structure: [ka]

[0075] In embodiments, the polypeptide conjugate of formula IC may have the following structure: [ka]

[0076] peptide Peptides for use in the polypeptide conjugates disclosed herein can be any peptide containing at least one region having an α-helical structure. α-Helices are common secondary structural motifs that play an important functional role in many proteins. In embodiments, the peptide may be predominantly α-helical, or the peptide may be part of a larger protein that contains one or more α-helical regions. As described above, the staples are appropriately positioned to substantially maintain the α-helical structure.

[0077] Peptides may be naturally occurring or specifically designed to interact with a target (e.g., inhibit protein-protein interactions). In some embodiments, peptides may be derived from naturally occurring peptides, with appropriate modifications to facilitate conjugation with staples, linkers, and / or cCPPs, or combinations thereof. Thus, the amino acids in a peptide (X, Z, U, J, Y1, Y2, and Z', in each case and when present) are independently selected from any natural or unnatural amino acid and independently refer to amino acids naturally occurring in or introduced into the peptide. The term "unnatural amino acid" refers to an organic compound that is an analog of a natural amino acid in that it has a structure similar to that of a natural amino acid so as to mimic the structure and reactivity of a natural amino acid. An unnatural amino acid may be a modified amino acid and / or an amino acid analog that is not one of the 20 commonly occurring naturally occurring amino acids or the rare, minor natural amino acids selenocysteine ​​or pyrrolysine. An unnatural amino acid may also be a D-isomer of a natural amino acid. Examples of suitable amino acids include, but are not limited to, alanine, allosoleucine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, napthylalanine, phenylalanine, proline, pyroglutamic acid, serine, threonine, tryptophan, tyrosine, valine, 2,3-diaminopropionic acid derivatives, or combinations thereof. These and others, along with their abbreviations used herein, are listed in Table 1. [Table 1] *One-letter abbreviations: when shown in capital letters herein, they refer to the L-amino acid form; when shown in lower case letters herein, they refer to the D-amino acid form.

[0078] In some embodiments, Y1 is an amino acid having a side chain that forms a first linking group (b1) to the staple, and Y2 is an amino acid having a side chain that forms a second linking group (b2) to the staple. Thus, the precursors of each of Y1 and Y2 can independently be any amino acid having a side chain that is suitable, or can be modified to be suitable, for covalently linking a staple. Non-limiting examples of such amino acids include cysteine, glutamine, asparagine, and lysine, and analogs thereof (e.g., with additional carbohydrates in the side chain, such as homocysteine).

[0079] Further examples of amino acid analogs that can be incorporated into the peptides disclosed herein include those with alkene, alkyne, or nitrile side chains, because these side chains can be utilized to form staples (e.g., during ring-closing metathesis between olefins or two alkene-containing side chains) or to graft staples. In yet other embodiments, the precursor of Y1 can be an amino acid with a side chain suitable for covalent attachment (e.g., amide bond formation) to the side chain of the precursor of Y2. In such embodiments, the "reaction product" between the side chains of these amino acid analogs is a staple. For example, in certain embodiments, the precursor of Y1 is lysine and the precursor of Y2 is aspartic acid, and the amino group on the side chain of the Y1 precursor reacts with the carboxyl group on the side chain of the Y2 precursor to form an amide, which is a staple. As another example, the precursor of Y1 can be an amino acid analog with an alkyne on the side chain, and the precursor of Y2 can be an amino acid with an azide on the side chain; these groups react to form a triazole.

[0080] In particular, in embodiments, the peptide may include one or more amino acids having a side chain containing a thiol group (i.e., prior to conjugation to the linker, cCPP, and / or staple). The thiol group may be used to conjugate with the cCPP, linker, and / or staple by forming a thioether, thioester, or disulfide. Non-limiting examples of amino acid analogs having a thiol group include cysteine, homocysteine, and any of the following amino acid analogs: [ka]

[0081] As mentioned above, the above groups are precursors that allow for the attachment of staples, linkers, and / or cCCPs. Specifically, to attach a staple, linker, and / or cCCP to a peptide, the thiol hydrogen of the above groups is replaced with a bond to the staple, linker, or cCCP.

[0082] One example of a peptide for use in the present invention is a ligand of the MDM2 protein, such as the α-helical peptide Ac-LTFEHYWAQLTS (SEQ ID NO: 1) ("PDI"). This ligand can bind to the MDM2 protein and thereby disrupt the interaction between MDM2 and p53. Peptides that disrupt the MDM2 / p53 interaction may be useful for many applications, including, but not limited to, the control of soft tissue sarcomas, which overexpress MDM2 in the presence of wild-type p53. These cancers are maintained by interference with small molecules that block MDM2, thereby preventing p53 repression. The peptides of the present invention may be synthesized by methods well known to those of skill in the art. For example, peptides may be synthesized using standard solid-phase peptide synthesis (SPPS).

[0083] Staples The staples described herein stabilize the α-helical structure of bioactive peptides, conferring, for example, protease resistance, cell permeability, and biological activity. The staples may be any artificial fastener capable of holding a peptide in an α-helical structure. In embodiments, the staples reinforce the native α-helical structure of the peptide, thereby maintaining its binding affinity for its protein target.

[0084] Methods of peptide stapling are known to those skilled in the art. In some embodiments, peptide stapling may require the production of a polypeptide comprising two natural or unnatural amino acids (i.e., precursors of Y1 and Y2) having side chains containing functional groups suitable for stapling. In certain embodiments, the precursors of Y1 and Y2 may react to form a staple. In other embodiments, the precursors of Y1 and Y2 have side chains suitable for attaching a staple (i.e., a side chain, b1 or b2, containing an appropriate functional group for attaching a staple by forming a linking group). In still other embodiments, a staple is formed by replacing an intramolecular hydrogen bond with a covalent bond, e.g., by replacing a hydrogen atom and a carbonyl group on opposing amino acids involved in an intramolecular hydrogen bonding interaction with a group that bridges the opposing amino acids. Examples of such modifications are found in Joy, ST et al., Chem. Commun (Camb.) 52(33), 5738-5741, and Zhao, H. et al. Angew. Chem. Int. Ed. 2016, 55, 12088-12093, each of which is incorporated herein by reference in its entirety.

[0085] The amino acids forming or attached to the staples are typically spaced apart in the peptide chain so that their side chains are on substantially the same face of the folded peptide. Thus, in the case of an α-helical peptide, the amino acid side chains are usually arranged on substantially the same face of the α-helix. The distance between opposing amino acids on the same face of the peptide per turn of the helix is ​​approximately 5.4 Å. Accordingly, in various embodiments, the staple is any suitable moiety that holds these opposing amino acids at a distance of approximately 5.4 Å, thereby maintaining the α-helical structure. Thus, in embodiments, the staple can have a size ranging from about 5 Å to about 6 Å, from about 10 Å to about 12 Å, from about 15 Å to about 17 Å, from about 21 Å to about 23 Å, from about 26 Å to about 28 Å, and from about 31 Å to about 34 Å, including all values ​​and subranges therebetween. In other embodiments, the staples may have a size of about 5 Å, about 5.5 Å, about 6 Å, about 10.5 Å, about 11 Å, about 11.5 Å, about 12 Å, about 16.5 Å, about 17 Å, about 17.5 Å, about 22 Å, about 22.5 Å, about 23 Å, about 23.5 Å, about 25.5 Å, about 26 Å, about 26.5 Å, about 27 Å, about 27.5 Å, about 28 Å, about 28.5 Å, about 30.5 Å, about 31 Å, about 31.5 Å, about 32 Å, about 32.5 Å, about 33 Å, about 33.5 Å, about 34 Å, or about 34.5 Å.

[0086] For single turn stapling in an α-helix, the amino acids to which the staple is attached are generally at positions i, i+4. For two turn stapling in an α-helix, the amino acids to which the staple is attached are generally at positions i, i+7. For three turn stapling in an α-helix, the amino acids to which the staple is attached are generally at positions i, i+11. In other embodiments, the polypeptide conjugates disclosed herein can comprise two or more staples (also referred to as stitched peptides). For example, staples can be placed at positions i, i+4, and i+7, i+11.

[0087] In various embodiments, the number of amino acids between Y1 and Y2, i.e., "c" in Formulas IA-IC, is a suitable number of amino acids such that the staples are positioned on substantially the same face of the alpha helix. In embodiments, c is at least 3. In other embodiments, c is a number ranging from 3 to 30. In still other embodiments, c is 3, 6, or 10.

[0088] In some embodiments, the staple is selected from the group consisting of alkylene, N-alkylene, alkenylene, alkynylene, aryl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, and heteroaryl, each optionally substituted. Non-limiting examples of staples include lactam staples, hydrocarbon staples, CuAAC staples, bisthioether staples, perfluorobenzene staples, and thioether staples.

[0089] Many alternative stapling methods are known to those skilled in the art, each using a different form of macrocyclization chemistry and resulting in stapled peptides with different bioactive properties. For example, stapling can be one-component stapling. One-component stapling involves a direct bond-forming reaction between the side chains of two amino acids. In some embodiments, one-component stapling techniques can involve the formation of amide bonds between the side chains of amino acids in a peptide. In some embodiments, one-component stapling techniques can include, for example, ring-closing metathesis, lactamization, cycloaddition (e.g., Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), "click reaction"), reversible reactions (e.g., formation of disulfide bridges or oxime linkages), or thioether formation. Alternatively, the stapling technique can be two-component stapling. Two-component stapling involves a bifunctional linker compound that reacts with two complementary natural or unnatural amino acids in a desired peptide to form a staple. Two-component stapling may use, for example, a photoswitchable linker or a functionalized "double-click" linker. When staples are attached using a click reaction, each of b1 and b2 is a triazole, optionally substituted. That is, in some embodiments, the precursors of Y1 and Y2 may independently be amino acid analogs bearing alkyne groups on the side chains or amino acids bearing azide groups on the side chains, and these groups react with staple precursors bearing complementary alkyne and / or azide groups to form triazoles. Click reactions may also be used to create staples using two-component stapling, in which case the staple is a triazole and b1 and b2 are absent. Thus, b1 and b2 may be linking groups formed when attached to a peptide for stapling using any of the above techniques. In some embodiments, each of b1 and b2 is independently absent or selected from aryl (eg, triazole), thioether, disulfide, amide, ester, and ether.

[0090] Additional examples of staples and stapling methods suitable for use in the stapled peptides of the present invention are described in Walensky, LD, et al., J. Med. Chem., 57, 6275-6288 (2014), Lau, YH, et al., Chem. Soc. Rev., 00, 1-12 (2014), Joy, ST et al., Chem. Commun (Camb.) 52(33), 5738-5741), and Zhao, H. et al. Angew. Chem. Int. Ed. 2016, 55, 12088-12093, each of which is incorporated herein by reference in its entirety.

[0091] Cyclic cell-penetrating peptides (cCPPs) Cyclic cell-penetrating peptides enable delivery of otherwise impermeable stapled peptides for efficient delivery to the cytosol and nucleus of the cell. The cCPP of the polypeptide conjugates disclosed herein can be or contain any amino acid sequence that facilitates cellular uptake of the polypeptide conjugates disclosed herein. cCPPs suitable for use in the polypeptide conjugates and methods described herein can include naturally occurring, modified, and synthetic sequences. In embodiments, the total number of amino acids in the cCPP can range from 4 to about 20 amino acids, e.g., about 5, about 6, about 7, about 8, about 9, about 10, about 11, about 12, about 13, about 14, about 15, about 16, about 17, about 18, and about 19 amino acids, including all ranges and subranges therebetween. In some embodiments, the cCPPs disclosed herein contain from about 4 to about 13 amino acids. In certain embodiments, the CPPs disclosed herein contain from about 6 to about 10 amino acids, or from about 6 to about 8 amino acids.

[0092] Each amino acid of a cCPP can independently be a natural or unnatural amino acid.

[0093] In some embodiments, a cCPP may include any combination of at least two arginines and at least two hydrophobic amino acids, hi some embodiments, a cCPP may include any combination of two to three arginines and at least two hydrophobic amino acids.

[0094] In some embodiments, a cCPP used in a polypeptide conjugate described herein has a structure comprising Formula 3: [ka] During the ceremony, each of AAl, AA2, AA3, and AA4 is independently selected from a D-amino acid or an L-amino acid; AA u and A.A. z is independently selected from a D-amino acid or an L-amino acid in each occurrence and when present, and m and n are independently selected from the numbers 0 to 6; During the ceremony, At least two AAs u , if present, AA1, AA2, AA3, AA4, and AA z is independently arginine, if present; and At least two AAs u , if present, AA1, AA2, AA3, AA4, and AA z , when present, are independently hydrophobic amino acids.

[0095] In some embodiments, each hydrophobic amino acid is independently selected from glycine, alanine, valine, leucine, isoleucine, methionine, phenylalanine, tryptophan, proline, naphthylalanine, phenylglycine, homophenylalanine, tyrosine, cyclohexylalanine, piperidine-2-carboxylic acid, cyclohexylalanine, norleucine, 3-(3-benzothienyl)-alanine, 3-(2-quinolyl)-alanine, O-benzylserine, 3-(4-(benzyloxy)phenyl)-alanine, S-(4-methylbenzyl)cysteine, N-(naphthalen-2-yl)glutamine, 3-(1,1'-biphenyl-4-yl)-alanine, tert-leucine, or nicotinoyllysine, each of which is optionally substituted with one or more substituents. The structures of some of these non-natural aromatic hydrophobic amino acids (prior to incorporation into the peptides disclosed herein) are provided below. In certain embodiments, each hydrophobic amino acid is independently a hydrophobic aromatic amino acid.In some embodiments, the aromatic hydrophobic amino acid is naphthylalanine, phenylglycine, homophenylalanine, phenylalanine, tryptophan, or tyrosine, each of which is optionally substituted with one or more substituents.In certain embodiments, the hydrophobic amino acid is piperidine-2-carboxylic acid, naphthylalanine, tryptophan, or phenylalanine, each of which is optionally substituted with one or more substituents. [ka]

[0096] The optional substituents can be any atoms or groups that do not significantly reduce the cytosolic delivery efficiency of the cCPP, for example, substituents that do not reduce the relative cytosolic delivery efficiency below that of c(FΦRRRRQ). In some embodiments, the optional substituents can be hydrophobic or hydrophilic. In certain embodiments, the optional substituents are hydrophobic substituents. In some embodiments, the substituents increase the solvent-accessible surface area (as defined herein) of the hydrophobic amino acid. In some embodiments, the substituents can be halogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, aryl, heteroaryl, alkoxy, aryloxy, acyl, alkylcarbamoyl, alkylcarboxamidyl, alkoxycarbonyl, alkylthio, or arylthio. In some embodiments, the substituents are one or more halogen atoms.

[0097] Selecting amino acids with higher hydrophobicity values ​​can improve the cytosolic delivery efficiency of cCPPs compared to amino acids with lower hydrophobicity values. In some embodiments, each hydrophobic amino acid independently has a hydrophobicity value greater than that of glycine. In other embodiments, each hydrophobic amino acid independently has a hydrophobicity value greater than that of alanine. In still other embodiments, each hydrophobic amino acid independently has a hydrophobicity value equal to or greater than that of phenylalanine. Hydrophobicity may be measured using hydrophobicity scales well known in the art. Table 2 below shows the hydrophobicity values ​​of various amino acids reported by Eisenberg and Weiss (Proc. Natl. Acad. Sci. USA 1984;81(1):140-144), Engleman, et al. (Ann. Rev. of Biophys. Biophys. Chem. 1986;1986(15):321-53), Kyte and Doolittle (J. Mol. Biol. 1982;157(1):105-132), Hoop and Woods (Proc. Natl. Acad. Sci. USA 1981;78(6):3824-3828), and Janin (Nature. 1979;277(5696):491-492), the entire contents of each of which are incorporated herein by reference in their entirety. In certain embodiments, hydrophobicity is measured using the hydrophobicity scale reported in Engleman, et al. [Table 2]

[0098] The chirality of amino acids can be selected to improve the efficiency of uptake into the cytosol. In some embodiments, at least two amino acids have opposite chirality. In some embodiments, at least two amino acids of opposite chirality can be adjacent to each other. In some embodiments, at least three amino acids have alternating stereochemistry relative to each other. In some embodiments, the at least three amino acids of alternating chirality relative to each other can be adjacent to each other. In some embodiments, at least two amino acids have the same chirality. In some embodiments, at least two amino acids of the same chirality can be adjacent to each other. In some embodiments, at least two amino acids have the same chirality and at least two amino acids have opposite chirality. In some embodiments, at least two amino acids of opposite chirality can be adjacent to at least two amino acids of the same chirality. Thus, in some embodiments, adjacent amino acids in a cCPP can have any of the following sequences: DL; LD; DLLD; LDDL; LDLLD; DLDDL; DLDDL; or LDDLD.

[0099] In some embodiments, the arginine is adjacent to a hydrophobic amino acid. In some embodiments, the arginine has the same chirality as the hydrophobic amino acid. In some embodiments, at least two arginines are adjacent to one another. In yet other embodiments, three arginines are adjacent to one another. In some embodiments, at least two hydrophobic amino acids are adjacent to one another. In other embodiments, at least three hydrophobic amino acids are adjacent to one another. In other embodiments, the cCPPs described herein comprise at least two consecutive hydrophobic amino acids and at least two consecutive arginines. In further embodiments, one hydrophobic amino acid is adjacent to one of the arginines. In still other embodiments, the cCPPs described herein comprise at least three consecutive hydrophobic amino acids and consecutive arginines therebetween. In further embodiments, one hydrophobic amino acid is adjacent to one of the arginines. Various combinations of these amino acids can have any arrangement of D and L amino acids, for example, the sequences described above.

[0100] In some embodiments, any four adjacent amino acids in a cCPP described herein (e.g., a cCPP according to Formula 2) can have one of the following sequences: AA H2 -AA H1 -Rr, AA H2 -AA H1 -rR, Rr-AA H1 -AA H2 , or rR-AA H1 -AA H2 , where AA H1 and A.A. H2 are each independently a hydrophobic amino acid. Thus, in some embodiments, the cCPP used in the polypeptide conjugates described herein has the formula 4A-D: [ka] During the ceremony, AA H1 and A.A. H2each of which is independently a hydrophobic amino acid; In each case and if present, AA U and A.A. Z are each independently any amino acid; m and n are independently selected from the numbers 0 to 6; The sequence includes any one of the following:

[0101] In some embodiments, the amino acids (r, R, AA) in the cCPPs of Formulas 4-A to 4-D H1 , A.A. H2 The total number of amino acids (inclusive) ranges from 6 to 10. In some embodiments, the total number of amino acids is 6. In some embodiments, the total number of amino acids is 7. In some embodiments, the total number of amino acids is 8. In some embodiments, the total number of amino acids is 9. In some embodiments, the total number of amino acids is 10.

[0102] In some embodiments, the sum of m and n is between 2 and 6. In some embodiments, the sum of m and n is 2. In some embodiments, the sum of m and n is 3. In some embodiments, the sum of m and n is 4. In some embodiments, the sum of m and n is 5. In some embodiments, the sum of m and n is 6. In some embodiments, m is 0. 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, 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 6.

[0103] In some embodiments, each hydrophobic amino acid is independently selected from glycine, alanine, valine, leucine, isoleucine, methionine, phenylalanine, tryptophan, proline, naphthylalanine, phenylglycine, homophenylalanine, tyrosine, cyclohexylalanine, piperidine-2-carboxylic acid, cyclohexylalanine, norleucine, 3-(3-benzothienyl)-alanine, 3-(2-quinolyl)-alanine, O-benzylserine, 3-(4-(benzyloxy)phenyl)-alanine, S-(4-methylbenzyl)cysteine, N-(naphthalen-2-yl)glutamine, 3-(1,1'-biphenyl-4-yl)-alanine, tert-leucine, or nicotinoyllysine, each of which is optionally substituted with one or more substituents. In certain embodiments, each hydrophobic amino acid is independently a hydrophobic aromatic amino acid. In some embodiments, the aromatic hydrophobic amino acid is naphthylalanine, phenylglycine, homophenylalanine, phenylalanine, tryptophan, or tyrosine, each of which is optionally substituted with one or more substituents. In certain embodiments, the hydrophobic amino acid is piperidine-2-carboxylic acid, naphthylalanine, tryptophan, or phenylalanine, each of which is optionally substituted with one or more substituents.

[0104] In some embodiments, AA H1 and A.A. H2 are independently hydrophobic amino acids having a hydrophobicity value greater than the hydrophobicity value of glycine. H1 and A.A. H2 are independently hydrophobic amino acids having a hydrophobicity value greater than the hydrophobicity value of alanine. H1 and A.A. H2are each independently a hydrophobic amino acid having a hydrophobicity value greater than that of phenylalanine, as measured using the hydrophobicity scales described above, including, for example, Eisenberg and Weiss (Proc. Natl. Acad. Sci. USA 1984;81(1):140-144), Engleman, et al. (Ann. Rev. of Biophys. Biophys. Chem. 1986;1986(15):321-53), Kyte and Doolittle (J. Mol. Biol. 1982;157(1):105-132), Hoop and Woods (Proc. Natl. Acad. Sci. USA 1981;78(6):3824-3828), and Janin (Nature. 1979;277(5696):491-492), (see Table 1 above). In certain embodiments, hydrophobicity is measured using the hydrophobicity scale reported in Engleman, et al.

[0105] The presence or combination of hydrophobic amino acids at the N- or C-terminus of D-Arg or L-Arg has also been shown to improve uptake of cCPPs (and attached cargo) into cytosols. For example, in some embodiments, the cCPPs disclosed herein contain AA H1 -D-Arg or D-Arg-AA H1 In other embodiments, the cCPPs disclosed herein may comprise AA H1 -L-Arg or L-Arg-AA H1 may include:

[0106] D-Arg or L-Arg at the N- or C-terminus, or a combination thereof (i.e., AA H1The size of the hydrophobic amino acids on the CPP may be selected to improve the cytosolic delivery efficiency of the CPP. For example, a larger hydrophobic amino acid at the N-terminus or C-terminus of D-Arg or L-Arg, or a combination thereof, improves cytosolic delivery efficiency compared to an otherwise identical sequence having a smaller hydrophobic amino acid. The size of the hydrophobic amino acid can be measured by the molecular weight of the hydrophobic amino acid, the steric effect of the hydrophobic amino acid, the solvent-accessible surface area (SASA) of the side chain, or a combination thereof. In some embodiments, the size of the hydrophobic amino acid is measured in terms of the molecular weight of the hydrophobic amino acid, whereby a larger hydrophobic amino acid has a side chain with a molecular weight of at least about 90 g / mol, or at least about 130 g / mol, or at least about 141 g / mol. In other embodiments, the size of the amino acid is measured in terms of the SASA of the hydrophobic side chain, whereby a larger hydrophobic amino acid has a side chain with a SASA greater than alanine or greater than glycine. In other embodiments, the size of the hydrophobic amino acid is measured in terms of the SASA of the hydrophobic side chain, whereby a larger hydrophobic amino acid has a side chain with a SASA greater than alanine or greater than glycine. H1 has a hydrophobic side chain with a SASA of about piperidine-2-carboxylic acid or greater, about tryptophan or greater, about phenylalanine or greater, or about naphthylalanine or greater. In some embodiments, AA H1 is at least about 200 Å 2 , at least about 210 Å 2 , at least about 220 Å 2 , at least about 240 Å 2 , at least about 250 Å 2 , at least about 260 Å 2 , at least about 270 Å 2 , at least about 280 Å 2 , at least about 290 Å 2 , at least about 300 Å 2 , at least about 310 Å 2 , at least about 320 Å 2 or at least about 330 Å. In some embodiments, AA2 has a side chain with a SASA of at least about 200 Å. 2 , at least about 210 Å 2 , at least about 220 Å2 , at least about 240 Å 2 , at least about 250 Å 2 , at least about 260 Å 2 , at least about 270 Å 2 , at least about 280 Å 2 , at least about 290 Å 2 , at least about 300 Å 2 , at least about 310 Å 2 , at least about 320 Å 2 , or at least about 330 Å 2 In some embodiments, the side chains of AA1 and AA2 have a SASA of at least about 350 Å. 2 , at least about 360 Å 2 , at least about 370 Å 2 , at least about 380 Å, at least about 390 Å 2 , at least about 400 Å 2 , at least about 410 Å 2 , at least about 420 Å 2 , at least about 430 Å 2 , at least about 440 Å 2 , at least about 450 Å 2 , at least about 460 Å 2 , at least about 470 Å 2 , at least about 480 Å 2 , at least about 490 Å 2 , about 500Å 2 at least about 510 Å 2 , at least about 520 Å 2 , at least about 530 Å 2 , at least about 540 Å 2 , at least about 550 Å 2 , at least about 560 Å 2 , at least about 570 Å 2 , at least about 580 Å 2 , at least about 590 Å 2 , at least about 600 Å 2 , at least about 610 Å 2 , at least about 620 Å 2 , at least about 630 Å 2 , at least about 640 Å 2, approximately 650 Å 2 Greater than about 660 Å 2 , at least about 670 Å 2 , at least about 680 Å 2 , at least about 690 Å 2 , or at least about 700 Å 2 In some embodiments, the SASA is a combination of AA H2 AA H1 and a hydrophobic amino acid having a side chain with a SASA that is equal to or less than the SASA of the hydrophobic side chain of (I) . By way of example and not limitation, a cCPP having a NaI-Arg motif exhibits improved cytosolic delivery efficiency compared to an otherwise identical CPP having a Phe-Arg motif; a cCPP having a Phe-NaI-Arg motif exhibits improved cytosolic delivery efficiency compared to an otherwise identical cCPP having a NaI-Phe-Arg motif; and a phe-NaI-Arg motif exhibits improved cytosolic delivery efficiency compared to an otherwise identical cCPP having a NaI-Phe-Arg motif.

[0107] As used herein, "hydrophobic surface area" or "SASA" refers to the solvent-accessible surface area of ​​an amino acid side chain (reported as square angstroms; Å 2 ) In certain embodiments, SASA is calculated using the "rolling ball" algorithm developed by Shrake & Rupley (J Mol Biol. 79(2):351-71), which is incorporated herein by reference in its entirety for all purposes. This algorithm probes the surface of the molecule using a solvent "sphere" of a specific radius. A typical value for the sphere is 1.4 Å, which approximates the radius of a water molecule.

[0108] SASA values ​​for certain side chains are provided in Table 3 below. In certain embodiments, the SASA values ​​described herein are based on the theoretical values ​​listed in Table 3 below, as reported by Tien, et al. (PLOS ONE 8(11):e80635. https: / / doi.org / 10.1371 / journal.pone.0080635), which is incorporated herein by reference in its entirety for all purposes. [Table 3]

[0109] In some embodiments, the cCPP is AA H2 -AA H1 -Rr, AA H2 -AA H1 -rR, Rr-AA H1 -AA H2 , or rR-AA H1 -AA H2 In an alternative embodiment, the cCPP does not contain hydrophobic amino acids on the N-terminus and / or C-terminus of AA H1 or AA H2 In yet another embodiment, the cCPP does not contain hydrophobic amino acids with a side chain (as described herein) larger than at least one of AA H1 does not contain hydrophobic amino acids with a surface area greater than AA H1 or AA H2 In embodiments where at least one of is phenylalanine, the cCPP is H1 or AA H2 In yet other embodiments, the cCPP contains at least one hydrophobic amino acid smaller than AA, e.g., leucine, but does not further contain naphthylalanine. H2 -AA H1 -Rr, AA H2 -AA H1 -rR, Rr-AA H1 -AA H2 , or rR-AA H1 -AA H2 In addition to the hydrophobic amino acids, it does not contain naphthylalanine.

[0110] The chirality of the c amino acid (i.e., D or L amino acid) can be selected to improve the cytosolic delivery efficiency of the cCPP (and any attached cargo, as described below). In some embodiments, arginine (e.g., AA H1 In some embodiments, the N- or C-terminal hydrophobic amino acid of AA H1 has the opposite chirality to the adjacent arginine. For example, if arginine is D-arg (i.e., "r"), then AA H1 is D-AA H1 and when arginine is L-Arg (i.e., "R"), AA H1 is L-AA H1 Thus, in some embodiments, the cCPPs disclosed herein may comprise at least one of the following motifs: D-AA H1 -D-arg, D-arg-D-AA H1 , L-AA H1 -L-Arg, or L-Arg-LAA H1 In certain embodiments, when arginine is D-arg, AA H can be D-nal, D-trp, or D-phe. In another non-limiting example, when arginine is L-Arg, AA H can be L-Nal, L-Trp, or L-Phe.

[0111] In some embodiments, the cCPPs described herein comprise three arginines. Thus, in some embodiments, the cCPPs described herein comprise one of the following sequences: AA H2 -AA H1 -RrR, AA H2 -AA H1 -Rrr, AA H2 -AA H1 -rRR, AA H2 -AA H1 -rRr, RRRr-AA H1 -AA H2, rRr-AA H1 -AA H2 , rrR-AA H1 -AA H2 , or RrR-AA H1 -AA H2 In certain embodiments, the cCPPS has the following sequence: AA H2 -AA H1 -RrR, AA H2 -AA H1 -rRr, rRr-AA H1 -AA H2 , or RrR-AA H1 -AA H2 In some embodiments, AAH1 and AAH2 can be selected to improve cytosolic uptake efficiency, e.g., as described above, where AAH1 has the same chirality as the adjacent arginine, and AAH1 and AAH2 have the opposite chirality.

[0112] In some embodiments, the cCPPs described herein comprise three hydrophobic amino acids. Thus, in some embodiments, the cCPPs described herein comprise one of the following sequences: AA H3 -AA H2 -AA H1 -Rr, AA H3 -AA H2 -AA H1 -Rr, AA H3 -AA H2 -AA H1 -rR,AA H3 -AA H2 -AA H1 -rR, Rr-AA H1 -AA H2 -AA H3 , Rr-AA H1 -AA H2 -AA H3 , rR-AA H1 -AA H2 -AA H3 , or rR-AA H1 -AA H2 -AA H3 Here is the AA H3is any hydrophobic amino acid described above, for example, piperidine-2-carboxylic acid, naphthylalanine, tryptophan, or phenylalanine. In some embodiments, AA H1 , A.A. H2 , and A.A. H3 The chirality of AAH1 may be selected to improve cytosolic uptake efficiency, for example, as described above, where AAH1 has the same chirality as the adjacent arginine, and AA H1 and A.A. H2 has the opposite chirality. In some embodiments, AA H1 , A.A. H2 , and A.A. H3 The size of AA may be selected to improve cytosolic uptake efficiency, for example, as described above. H3 AA H1 and A.A. H2 It has the following SAS:

[0113] In some embodiments, AA H1 and A.A. H2 have the same or opposite chirality. In certain embodiments, AA H1 and A.A. H2 have opposite chirality. Thus, in some embodiments, a cCPP disclosed herein comprises at least one of the following sequences: D-AA H2 -L-AA H1 -Rr;L-AA H2 -D-AA H1 -rR;RrD-AA H1 -L-AA H2 ; or rRL-AA H1 -D-AA H1 , where D-AA H1 and D-AA H2 are hydrophobic amino acids having the D configuration, and L-AA H1 and L-AA H2 are hydrophobic amino acids having the L configuration. In some embodiments, H1 and D-AA H2is independently selected from the group consisting of D-pip, D-nal, D-trp, and D-phe. H1 or D-AA H2 is D-nal. In other particular embodiments, D-AA H1 is D-nal. In some embodiments, L-AA H1 and L-AA H2 is independently selected from the group consisting of L-pip, L-Nal, L-Trp, and L-Phe. H1 or L-AA H2 are L-Nal, respectively.

[0114] As discussed above, the present disclosure provides various modifications to the cyclic peptide sequence, which may improve cytosolic delivery efficiency. In some embodiments, improved cytosolic uptake efficiency can be measured by comparing the cytosolic delivery of CPPs with modified sequences to appropriate control sequences. In some embodiments, the control sequence may contain specific modifications (e.g., R and AA). H1 In another embodiment, the control has the following sequence: cyclic (FΦRRRRQ).

[0115] As used herein, cytosolic delivery efficiency refers to the ability of cCPP to pass through the cell membrane and enter the cytosol. In embodiments, the cytosolic delivery efficiency of cCPP is not dependent on receptor or cell type. Cytosolic delivery efficiency can refer to absolute cytosolic delivery efficiency or relative cytosolic delivery efficiency.

[0116] Absolute cytosolic delivery efficiency is the ratio of the cytosolic concentration of cCPP (or polypeptide conjugate) to the concentration of cCPP (or polypeptide conjugate) in the growth medium. Relative cytosolic delivery efficiency refers to the concentration of cCPP in the cytosol compared to the concentration of control cCPP in the cytosol. Quantification can be achieved by fluorescently labeling the cCPP (e.g., with FITC dye) and measuring fluorescence intensity using techniques well known in the art.

[0117] In certain embodiments, relative cytosolic delivery efficiency is determined by comparing (i) the amount of a cCPP of the present invention internalized by a cell type (e.g., HeLa cells) with (ii) the amount of a control cCPP internalized by the same cell type. To measure relative cytosolic delivery efficiency, the cell type is incubated in the presence of a cell-penetrating peptide of the present invention for a specific period of time (e.g., 30 minutes, 1 hour, 2 hours, etc.), after which the amount of cCPP internalized by the cells is quantified using methods well known in the art, such as fluorescence microscopy. Separately, the same concentration of the control cCPP is incubated in the presence of the cell type for the same period of time, and the amount of the control cCPP internalized by the cells is quantified.

[0118] In another embodiment, the relative cytosolic delivery efficiency is determined by the IC of cCPPs with modified sequences of intracellular targets. 50 Measure the IC of cCPP with modified sequences 50 can be determined by comparison to an appropriate control sequence (as described herein).

[0119] In some embodiments, the relative cytosolic delivery efficiency of the cCPPs described herein, compared to, for example, cyclic (FΦRRRRQ) or linear cell-penetrating peptide sequences (e.g., HIV-TAT, polyarginine sequences, etc.), ranges from about 1% to about 1000%, e.g., about 1%, about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 100%, about 110%, etc. ,approximately 120%,approximately 130%,approximately 140%,approximately 150%,approximately 160%,approximately 170%,approximately 180%,approximately 190%,approximately 200%,approximately 210%,approximately 220%,approximately 230%,approximately 240%,approximately 250%,approximately 260%,approximately 270%,approximately 280%,approximately 290%,approximately 300%,approximately 310%,approximately 320%,approximately 330%,approximately 340%,approximately 350%,approximately 360%,approximately 370%,approximately 380%,approximately 390%,approximately 400%,approximately 410%,approximately 420%, About 430%, about 440%, about 450%, about 460%, about 470%, about 480%, about 490%, about 500%, about 510%, about 520%, about 530%, about 540%, about 550%, about 560%, about 570%, about 580%, or about 590%, about 600%, about 610%, about 620%, about 630%, about 640%, about 650%, about 660%, about 670%, about 680%, about 690%, about 700%, about 710%, about 720%, about 730% %, about 740%, about 750%, about 760%, about 770%, about 780%, or about 790%, about 800%, about 810%, about 820%, about 830%, about 840%, about 850%, about 860%, about 870%, about 880%, about 890%, about 900%, about 910%, about 920%, about 930%, about 940%, about 950%, about 960%, about 970%, about 980%, or about 1000%, including all values ​​and subranges therebetween.

[0120] In other embodiments, an absolute cytosolic delivery efficiency of about 40% to about 100%, e.g., about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, 80%, about 85%, about 90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99%, including all values ​​and subranges therebetween.

[0121] Non-limiting examples of suitable cyclic cell-penetrating peptides are provided in Table 4. [Table 4] [Table 5] [Table 6] [Table 7] Φ, L-2-naphthylalanine; Pim, pimelic acid; Nlys, lysine peptoid residue; D-pThr, D-phosphothreonine; Pip, L-piperidine-2-carboxylic acid; Cha, L-3-cyclohexylalanine; Tm, trimesic acid; Dap, L-2,3-diaminopropionic acid; Sar, sarcosine; F2Pmp, L-difluorophosphonomethylphenylalanine; Dod, dodecanoyl; Pra, L-propargylglycine; AzK, L-6-azido-2-amino-hexanoic acid; Agp, L-2-amino-3-guanidinylpropionic acid; b cyclization between Pim and Nlys; c cyclization between Lys and Glu; d Macrocyclization via multicomponent reaction with aziridine aldehydes and isocyanides; e backbone intercyclization of Gln residues; f the N-terminal amines and side chains of two Dap residues bicyclized at Tm; g three Cys side chains bicyclized with tris(bromomethyl)benzene; h Click reaction cyclization between Pra and Azk.

[0122] Additionally, cCPPs used in the polypeptide conjugates and methods described herein can include any of the sequences disclosed in U.S. Patent Application No. 15 / 312,878 (U.S. Patent Application Publication No. 2017 / 0190743 A1); U.S. Patent Application No. 15 / 360,719 ((U.S. Patent Application Publication No. 2017 / 0355730); International Application No. / US2017 / 060881 (and resultant U.S. publication); and International Application No. / US2017 / 062951 (and resultant U.S. publication), each of which is incorporated by reference in its entirety for all purposes.

[0123] In some embodiments, cCPPs improve cytosolic delivery efficiency by about 1.1-fold to about 30-fold compared to linear cell-penetrating peptide sequences (e.g., HIV-TAT, polyarginine, etc.), e.g., about 1.2, about 1.3, about 1.4, about 1.5, about 1.6, about 1.7, about 1.8, about 1.9, about 2.0, about 2.5, about 3.0, about 3.5, about 4.0, about 4.5, about 5.0, about 5.5, about 6.0, about 6.5, about 7.0, about 7.5, about 8.0, about 8.5, about 9.0, about 10, about 10.5, about 11.0, about 11.5, about 12.0, about 12.5, about 13.0, about 13.5, about 14.0, about 14.5, about 15.0, about 15.5, about 16. 6.0, about 16.5, about 17.0, about 17.5, about 18.0, about 18.5, about 19.0, about 19.5, about 20, about 20.5, about 21.0, about 21.5, about 22.0, about 22.5, about 23.0, about 23.5, about 24.0, about 24.5, about 25.0, about 25.5, about 26.0, about 26.5, about 27.0, about 27.5, about 28.0, about 28.5, about 29.0, or about 29.5 times, including all value and subranges therebetween.

[0124] Linker As noted above, a cCPP can be directly conjugated to a staple peptide (e.g., by a covalent bond between the side chain of an amino acid on the cCPP and a suitable group on the staple peptide), or a linker can be used to conjugate the cCPP to the staple peptide. As used herein, "linker" refers to a moiety that forms a covalent bond between two or more components of a polypeptide conjugate disclosed herein (e.g., a cCPP and a staple or peptide-mediated staple peptide).

[0125] In various embodiments, the linker is covalently bonded to either an amino acid on the cCPP and an amino acid on the peptide or staple. The linker can be any moiety that joins two or more of the cCPP moiety, peptide, and staple. In some embodiments, the linker can be an amino acid. In other embodiments, the precursor of the linker can be any suitable molecule that can form two or more bonds with amino acids in the cCPP, peptide, staple, and combinations thereof. Thus, in various embodiments, the precursor of the linker has two or more functional groups, each of which can form covalent bonds with at least two of the cCPP moiety, peptide, and staple. For example, the linker can be covalently bonded to the N-terminus, C-terminus, or side chain, or combinations thereof, of any amino acid in the cCPP moiety, peptide, or staple. In certain embodiments, the linker forms a covalent bond between the cCPP and the peptide.

[0126] In some embodiments, the linker is selected from the group consisting of at least one amino acid, alkylene, alkenylene, alkynylene, aryl, cycloalkyl, cycloalkenyl, cycloalkynyl, heterocyclyl, heteroaryl, or ether, each of which may be optionally substituted as defined above. Non-limiting examples of linkers include polyethylene glycol optionally conjugated to a lysine residue.

[0127] In some embodiments, the linker is covalently bonded to the N-terminus or C-terminus of an amino acid on a staple peptide, or to the side chain of glutamine, asparagine, or lysine on a cCPP, peptide, or staple, or to a modified side chain of glutamine or asparagine (e.g., a reduced side chain bearing an amino group). In certain embodiments, the linker forms a bond with the side chain of glutamine on a cCPP. In other specific embodiments, the linkers described herein have the structure of L-1 or L-2: [ka] During the ceremony, AA s is the side chain or terminus of an amino acid on a peptide or staple; AA c is the side chain or terminus of an amino acid of a cCPP; p is an integer from 0 to 10; q is an integer from 1 to 50; It has.

[0128] In some embodiments, the linker can release the staple peptide from the cCPP after the polypeptide conjugate enters the cytosol of a cell. In some embodiments, the linker includes a group or forms a group after attachment to the cCPP, peptide, staple, or a combination thereof, that is cleaved after uptake of the polypeptide conjugate into the cytosol, thereby releasing the peptide. Non-limiting examples of physiologically cleavable linking groups include carbonate, thiocarbonate, triester, disulfide, sulfoxide, hydrazine, protease-cleavable dipeptide linkers, and the like.

[0129] For example, in embodiments, the linker is covalently attached to the staple peptide, e.g., via a disulfide bond, with the side chain of a cysteine ​​or cysteine ​​analog located on the staple peptide or cCPP. In some embodiments, the disulfide bond is formed between a thiol group on the precursor of the linker and the side chain of a cysteine ​​or amino acid analog bearing a thiol group on the peptide, and the bond to the hydrogen on each thiol group is replaced with a bond to a sulfur atom. Non-limiting examples of amino acid analogs bearing thiol groups that can be used with the polypeptide conjugates disclosed herein are described above.

[0130] treatment method As noted above, the polypeptide conjugates described herein can be used to treat or prevent a disease, disorder, or condition in a patient in need thereof. In some embodiments, treatment refers to the partial or complete alleviation, amelioration, relief, suppression, delay in onset, reduction in severity and / or incidence of a patient's disease, disorder, or condition.

[0131] As used herein, the terms "improve," "increase," "reduce," "decrease," and the like refer to a value relative to a control. In some embodiments, a suitable control is a baseline measurement, e.g., a measurement in the same individual prior to initiation of a treatment described herein, or a measurement in a control individual (or control individuals) in the absence of a treatment described herein.

[0132] The individual to be treated (also referred to as a "patient") is an individual (fetus, infant, child, adolescent, or adult) who has a disease, disorder, or condition or who is at risk of developing a disease, disorder, or condition.

[0133] In some embodiments, the individual is one who has recently been diagnosed with a disease, disorder, or condition. Typically, early treatment (initiating treatment as soon as possible after diagnosis) is important to minimize the effects of the disease, disorder, or condition and maximize the benefits of treatment.

[0134] In some embodiments, polypeptide conjugates can be used to treat individuals diagnosed with cancer. The polypeptide conjugates of the invention may be used, for example, to treat the following cancers: brain tumors, such as acoustic neuroma; astrocytomas, including fibrillary, protoplasmic, gemistocytary, anaplastic, and pilocytic astrocytomas; glioblastomas; gliosarcoma; pleomorphic xanthoastrocytoma; subependymal giant cell astrocytoma; and desmoplastic infantile astrocytoma; brain lymphomas; brain tumor metastases; pituitary tumors, including prolactinomas, pituitary incidentalomas, HGH-producing adenomas, and corticotrophic adenomas. adenoma, craniopharyngioma, medulloblastoma, meningioma and oligodendroglioma; neural tumors, for example, tumors of the autonomic nervous system such as neuroblastoma, ganglioneuroma, paraganglioma (pheochromocytoma, pheochromocytoma) and carotid body tumors, peripheral nervous system tumors such as amputation neuroma, neurofibroma, neurinoma (neurilemmoma, schwannoma), malignant schwannoma, and tumors of the central nervous system, for example, brain tumors and bone marrow tumors; intestinal cancers, for example, carcinomas of the rectum, colon, anus, duodenum, etc.; eyelid tumors (basal cell tumor or adenocarcinoma of the eyelid organ); retinoblastoma; carcinoma of the pancreas; carcinoma of the bladder; lung tumors (bronchial carcinoma, small-cell lung cancer (SCLC), non-small-cell lung cancer (NSCLC)). NSCLC), e.g., spindle cell carcinoma, adenocarcinoma (acinar, papillary, bronchioloalveolar) and large cell tracheal carcinoma (giant cell carcinoma, clear cell carcinoma); ductal carcinoma, e.g., ductal carcinoma, lobular carcinoma, mucinous carcinoma, tubular carcinoma, Paget's carcinoma; non-Hodgkin's lymphoma (B-lymphatic or T-lymphatic NHL), e.g., hairy cell leukemia, Burkitt's lymphoma, mycosis fungoides, etc.; Hodgkin's disease; uterine cancer (corpus carcinoma or endometrial carcinoma); CUP (Cancer of Unknown Primary) syndrome (cancer of unknown primary); ovarian cancer (ovarian carcinoma - mucinous or serous cyst, endometrial tumor, clear cell tumor, Brenner tumor); gallbladder cancer; bile duct cancer, e.g., Klatzkin's tumor; testicular cancer (embryonic or non-embryonic germ cell tumor);Laryngeal cancers, e.g., supraglottic, glottic, and subglottic tumors of the vocal cords; bone cancers, e.g., osteochondroma, chondroma, chondroblastoma, chondromyxoid fibroma, chondrosarcoma, osteoma, osteoid osteoma, osteoblastoma, osteosarcoma, non-ossifying osteofibroma, osteofibroma, desmoplastic osteofibroma, osteofibrosarcoma, malignant fibrous histiocytoma, osteoclastoma or giant cell tumor, Ewing's sarcoma, and plasmacytoma, head and neck tumors tumors (HNO tumors), for example, tumors of the lip and oral cavity (carcinomas of the lips, tongue, and oral cavity), nasopharyngeal carcinoma (tumors of the nose, lymphoepithelioma), pharyngeal carcinoma, oropharyngeal carcinoma, tonsillar carcinoma (carcinoma of the tonsils (malignoma)) and carcinoma of the tongue (base), hypopharyngeal carcinoma, laryngeal carcinoma (cancer of the larynx), tumors of the paranasal sinuses and nasal cavity, tumors of the salivary glands and ear; hepatocellular carcinoma (hepatocellular carcinoma (HCC)); leukemias, for example, acute leukemias such as acute lymphatic / lymphoblastic leukemia (ALL), acute myeloid leukemia (AML); chronic lymphatic leukemia (CLL), chronic myeloid leukemia (CLL) leukemia (CML); gastric cancer (papillary, tubular, or mucinous adenocarcinoma, adenosquamous carcinoma, squamous cell carcinoma, or undifferentiated carcinoma); malignant melanoma, such as superficial spreading melanoma (SSM), nodular melanoma (NMM), lentigo melanoma (LMM), acral melanoma (ALM), and amelanotic melanoma (AMM); renal carcinoma, such as renal cell carcinoma (adrenal nephroma or Grawitz tumor); esophageal cancer; penile cancer; prostate cancer; vaginal cancer or vaginal carcinoma; thyroid carcinoma, such as papillary carcinoma, follicular carcinoma, myeloid carcinoma, or anaplastic thyroid carcinoma; thymic carcinoma (thymoma); urethral cancer (urethral carcinoma, urothelial carcinoma) and vulvar cancer;

[0135] In other embodiments, the polypeptide conjugates may be used to treat inflammatory diseases or disorders, such as respiratory diseases, e.g., asthma and chronic obstructive pulmonary disease, chronic degenerative diseases, rheumatoid arthritis, osteoarthritis, osteoporosis, dermatological conditions, e.g., psoriasis, scleroderma, atopic dermatitis, ichthyosis, pemphigus, acne, skin aging or wrinkling, chronic demyelinating diseases, e.g., multiple sclerosis, inflammatory bowel diseases, e.g., ulcerative colitis or Crohn's disease, dental diseases, e.g., periodontal disease and gingivitis, inflammatory nail diseases such as nail psoriasis, lichen planus, alopecia areata, systemic lupus erythematosus, diabetic nephropathy, lupus nephritis, IgA nephropathy or glomerulonephritis, graft-versus-host disease, or eye conditions.

[0136] In other embodiments, the polypeptide conjugates are used to treat autoimmune diseases or conditions, including insulin-dependent diabetes mellitus, multiple sclerosis, rheumatoid arthritis, autoimmune uveitis, primary biliary cirrhosis, myasthenia gravis, Sjogren's syndrome, pemphigus vulgaris, scleroderma, pernicious anemia, systemic lupus erythematosus, Graves' disease, inflammatory bowel disease, celiac disease, autoimmune thyroid diseases such as Hashimoto's disease, autoimmune liver disease, Addison's disease, transplant rejection, graft-versus-host disease, host-versus-graft disease, ankylosing spondylitis, Chagas' disease, chronic obstructive pulmonary disease, and Crohn's disease. , dermatomyositis, endometriosis, Goodpasture's syndrome, Guillain-Barré syndrome (GBS), hidradenitis suppurativa, Kawasaki disease, IgA nephropathy, idiopathic thrombocytopenic purpura, interstitial cystitis, mixed connective tissue disease, morphea, narcolepsy, neuromyositis, psoriasis, psoriatic arthritis, polymyositis synovitis, relapsing polychondritis, sarcoidosis, schizophrenia, stiff-person syndrome, temporal arteritis, ulcerative colitis, vasculitis, vitiligo, Wegener's granulomatosis, and combinations thereof.

[0137] The polypeptide conjugates provided herein can treat the above-mentioned diseases, disorders, or conditions, for example, by interfering with natural protein-protein, protein-ligand, and / or protein-receptor interactions. For example, many biologically important protein / protein interactions, such as p53 / MDM2 and Bcl-Xl / Bak, are mediated by one protein donating a helix into the cleft of the other helix-accepting protein. The interaction between p53 and MDM2, as well as mutations in the p53 gene, have been identified in virtually half of all reported cancer cases (see Shair Chem. & Biol. 1997, 4.791, the entire contents of which are incorporated herein by reference). When cells are subjected to stress, p53 is thought to coordinate responses that lead to either cell cycle arrest and DNA repair or programmed cell death. Similar to mutations in the p53 gene, which directly alter the function of the p53 protein, p53 can also be altered by changes in MDM2. The MDM2 protein has been shown to bind to p53 and inhibit transcriptional activation by associating with the transactivation domain of p53. For example, an 11-amino acid peptide derived from the transactivation domain of p53 forms a 2.5-turn amphipathic α-helix that inserts into the MDM2 recess.

[0138] Treatment Combinations In some embodiments, the polypeptide conjugates disclosed herein can be administered in combination with other therapies. The polypeptide conjugates can be administered simultaneously, sequentially, or at different times as part of the same therapeutic regimen.

[0139] In some embodiments, the polypeptide conjugates disclosed herein are administered in combination with one or more chemotherapeutic agents. Chemotherapeutic agents that may be administered in combination with a compound according to the invention include, but are not limited to, hormones, hormone analogs, and antihormones (e.g., tamoxifen, toremifene, raloxifene, fivestrant, megestrol acetate, flutamide, nilutamide, bicalutamide, aminoglutethimide, cyproterone acetate, finasteride, buserelin acetate, fludrocortisone, fluoxymesterone, medroxyprogesterone, octreotide), aromatase inhibitors (e.g., anastrozole, letrozole, liarozole, vorozole, exemestane, atamestane), LHRH agonists and antagonists (e.g., goserelin acetate, leuprolide), inhibitors of growth factors (e.g., growth factors such as "platelet-derived growth factor" and "hepatocyte growth factor"). Inhibitors include, for example, "growth factor" antibodies, "growth factor receptor" antibodies, and tyrosine kinase inhibitors, such as gefitinib, lapatinib, and trastuzumab; signal transduction inhibitors (e.g., imatinib and sorafenib); antimetabolites (e.g., folate antagonists such as methotrexate, pemetrexed, and raltitrexed, 5-fluorouracil, capecitabine, and gemcitabine, pyrimidine analogs such as mercaptopurine, adenosine analogs such as thioguanine, cladribine, and pentostatin, cytarabine, and fludarin); antitumor antibiotics (e.g., anthracyclines such as doxorubicin, daunorubicin, epirubicin, idarubicin, mitomycin C, bleomycin, dactinomycin, plicanic acid, and streptozocin); platinum derivatives (e.g., cisplatin, oxaliplatin, and carboplatin);Alkylating agents (e.g., estramustine, meclorethamine, melphalan, chlorambucil, busulfan, dacarbazine, cyclophosphamide, ifosfamide, temozolomide, carmustine and lomustine, nitrosoureas such as thiotepa), antimitotic agents (e.g., vinca alkaloids such as vinblastine, vindesine, vinorelbine and vincristine; and taxanes such as paclitaxel and docetaxel). topoisomerase inhibitors (e.g., etoposide and epipodophyllotoxins such as etopophos, teniposide, amsacrine, topotecan, irinotecan, mitoxantrone), and various chemotherapeutic agents such as amifostine, anagrelide, clodronate, filgrastin, interferon alpha, leucovorin, rituximab, procarbazine, levamisole, mesna, mitotane, pamidronate, and porfimer.

[0140] Production method The polypeptide conjugates described herein can be prepared by a variety of methods well known to those skilled in the art of organic synthesis, or variations thereof, as will be appreciated by those skilled in the art. The compounds described herein can be prepared from readily available starting materials. Optimum reaction conditions may vary depending on the particular reactants or solvents used, but such conditions can be determined by one skilled in the art.

[0141] Variations of the compounds described herein include the addition, subtraction, or movement of various components as described for each compound. Similarly, if one or more chiral centers are present in the molecule, the chirality of the molecule can be altered. In addition, the synthesis of the compounds can include the protection and deprotection of various chemical groups. The use of protection and deprotection, and the selection of appropriate protecting groups, can be determined by those skilled in the art. The chemistry of protecting groups can be found, for example, in Wuts and Greene, Protective Groups in Organic Synthesis, 4th Ed., Wiley & Sons, 2006, which is incorporated herein by reference in its entirety.

[0142] Starting materials and reagents used in preparing the disclosed compounds and compositions are available from commercial suppliers, such as Aldrich Chemical Co.(Milwaukee, Wisconsin), Acros Organics (Morris Plains, New Jersey), Fisher Scientific (Pittsburgh, Pennsylvania), Sigma (St. Louis, Missouri), Pfizer (New York, New York), GlaxoSmithKline (Raleigh, North Carolina), Merck (Whitehouse Station, New Jersey), Johnson & Johnson (New Brunswick, New Jersey), Aventis (Bridgewater, New Jersey), AstraZeneca (Wilmington, Delaware), Novartis (Basel, Switzerland), Wyeth (Madison, New Jersey), Bristol-Myers-Squibb (New York, New York), Roche (Basel, Switzerland), Lilly (Indianapolis, Indiana), Abbott (Abbott Park, Illinois), Schering Plough (Kenilworth, New Jersey), or Boehringer Ingelheim (Ingelheim, Germany), or prepared by methods well known to those skilled in the art according to procedures described in the following references: Fieser and Fieser's Reagents for Organic Synthesis, Volumes 1-17 (John Wiley and Sons, 1991); Rodd's Chemistry of Carbon Compounds, Volumes 1-5 and Supplementals (Elsevier Science Publishers, 1989); Organic Reactions, Volumes 1-40 (John Wiley and Sons, 1991); March's Advanced Organic Chemistry, (John Wiley and Sons, 4th Edition); and Larock's Comprehensive Organic Transformations (VCH Publishers Inc., 1989). Other materials, such as the pharmaceutical carriers disclosed herein, may be obtained from commercial sources.

[0143] The reactions to produce the compounds described herein can be carried out in a solvent that can be selected by one skilled in the art of organic synthesis. The solvent can be substantially non-reactive with the starting materials (reactants), intermediates, or products under the conditions (i.e., temperature and pressure) under which the reaction is carried out. The reaction can be carried out in one solvent or a mixture of two or more solvents. The formation of the product or intermediate can be controlled by any suitable method known in the art. For example, the formation of the product can be controlled by spectroscopy, such as nuclear magnetic resonance spectroscopy (e.g., 1H or 13C), infrared spectroscopy, spectrophotometry (e.g., UV-visible), or mass spectrometry, or by chromatography, such as high-performance liquid chromatography (HPLC) or thin-layer chromatography.

[0144] The disclosed compounds can be prepared by solid-phase peptide synthesis, in which the α-N-terminus of the amino acid is protected with an acid or base protecting group. Such protecting groups should be stable to the conditions of peptide bond formation while being easily removed without disruption of the growing peptide chain or racemization of the chiral centers contained therein. Suitable protecting groups include 9-fluorenylmethyloxycarbonyl (Fmoc), t-butyloxycarbonyl (Boc), benzyloxycarbonyl (Cbz), biphenylisopropyloxycarbonyl, t-amyloxycarbonyl, isobornyloxycarbonyl, α,α-dimethyl-3,5-dimethoxybenzyloxycarbonyl, o-nitrophenylsulfenyl, and 2-cyano-t-butyloxycarbonyl. The 9-fluorenylmethyloxycarbonyl (Fmoc) protecting group is particularly preferred in the synthesis of the disclosed compounds. Other preferred side chain protecting groups are 2,2,5,7,8-pentamethylchroman-6-sulfonyl (pmc), nitro, p-toluenesulfonyl, 4-methoxybenzenesulfonyl, Cbz, Boc, and adamantyloxycarbonyl for side chain amino groups such as lysine and arginine; benzyl, o-bromobenzyloxycarbonyl, 2,6-dichlorobenzyl, isopropyl, t-butyl (t-Bu), cyclohexyl, cyclopenyl, and acetyl (Ac) for tyrosine; t-butyl, benzyl, and tetrahydropyranyl for serine; trityl, benzyl, Cbz, p-toluenesulfonyl, and 2,4-dinitrophenyl for histidine; formyl for tryptophan; benzyl and t-butyl for aspartic acid and glutamic acid, and triphenylmethyl (trityl) for cysteine. In solid-phase peptide synthesis, the α-C-terminal amino acid is attached to a suitable solid support or resin. Suitable solid supports useful in the above synthesis are those materials that are inert to the reagents and reaction conditions of the stepwise condensation-deprotection reactions, as well as insoluble in the media used.The solid support for synthesis of C-terminal carboxypeptides was 4-hydroxymethylphenoxymethyl-copoly(styrene-1% divinylbenzene) or 4-(2',4'-dimethoxyphenyl-Fmoc-aminomethyl)phenoxyacetamidoethyl resin, available from Applied Biosystems (Foster City, CA). The α-C-terminal amino acid is linked to the resin by N,N'-dicyclohexylcarbodiimide (DCC), N,N'-diisopropylcarbodiimide (DIC), or O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU), with or without 4-dimethylaminopyridine (DMAP), 1-hydroxybenzotriazole (HOBT), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP), or bis(2-oxo-3-oxazolidinyl)phosphine chloride (BOPCI), in a solvent such as dichloromethane or DMF, at a temperature between 10°C and 50°C for about 1 to about 24 hours. When the solid support is 4-(2',4'-dimethoxyphenyl-Fmoc-aminomethyl)phenoxy-acetamidoethyl resin, the Fmoc group is cleaved with a secondary amine, preferably piperidine, before coupling with the α-C-terminal amino acid, as described above. One method for coupling to this deprotected 4-(2',4'-dimethoxyphenyl-Fmoc-aminomethyl)phenoxy-acetamidoethyl resin is with O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU, 1 equivalent) and 1-hydroxybenzotriazole (HOBT, 1 equivalent) in DMF. The coupling of successive protected amino acids can be carried out in an automated polypeptide synthesizer. In one example, the α-N-terminus of the amino acid in the growing peptide chain is protected with Fmoc. Removal of the Fmoc protecting group from the α-N-terminal side of the growing peptide is achieved by treatment with a secondary amine, preferably piperidine.Next, each protected amino acid is preferably introduced in approximately a three-fold molar excess, and coupling is preferably carried out in DMF. The coupling agent can be O-benzotriazol-1-yl-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU, 1 equivalent) and 1-hydroxybenzotriazole (HOBT, 1 equivalent). At the end of solid-phase synthesis, the polypeptide is removed from the resin and then deprotected, either sequentially or in a single operation. Removal and deprotection of the polypeptide can be achieved in a single operation by treating the resin-bound polypeptide with a cleavage reagent containing thioanisole, water, ethanedithiol, and trifluoroacetic acid. If the α-C-terminus of the polypeptide is an alkylamide, the resin is cleaved by aminolysis with an alkyl group. Alternatively, the peptide can be removed by transesterification (e.g., with methanol), followed by aminolysis or direct transamination. The protected peptide can be purified at this point or used directly in the next step. Removal of side-chain protecting groups can be achieved using the cleavage cocktail described above. The fully deprotected peptide can be purified by a series of chromatographic procedures using any or all of the following types: ion exchange on a weakly basic resin (acetate form); hydrophobic adsorption chromatography on underivatized polystyrene-divinylbenzene (e.g., Amberite XAD); silica gel adsorption chromatography; ion exchange chromatography on carboxymethylcellulose; partition chromatography, e.g., Sephadex G-25, LH-20, or countercurrent distribution; high-performance liquid chromatography (HPLC), particularly reverse-phase HPLC on octyl- or octadecylsilyl-silica bonded phase column packings.

[0145] Administration method The in vivo application of the disclosed polypeptide conjugates and compositions containing them can be achieved by any suitable method and technique known to those skilled in the art, now or in the future. For example, the disclosed compounds can be formulated in a physiologically or pharmaceutically acceptable form and administered by any suitable route known in the art, including, for example, oral and parenteral administration. As used herein, the term parenteral includes, for example, subcutaneous, intradermal, intravenous, intramuscular, intraperitoneal, and intrasternal administration by injection. The administration of the disclosed compounds or compositions can be a single administration, or can be continuous or at discrete intervals, as can be easily determined by one skilled in the art.

[0146] The compounds disclosed herein and compositions comprising them can also be administered using liposome technology, sustained-release capsules, implantable pumps, and biodegradable containers.These delivery methods can advantageously provide a uniform dosage over a long period of time.The compounds can also be administered in their salt derivative form or crystalline form.

[0147] The compounds disclosed herein can be formulated by well-known methods for preparing pharmaceutically acceptable compositions. Formulations are described in detail in many sources known and readily available to those skilled in the art. For example, E.W. Martin's Remington's Pharmaceutical Science (1995) describes formulations that can be used with the disclosed methods. In general, the compounds disclosed herein can be formulated so that an effective amount of the compound is combined with a suitable carrier to facilitate effective administration of the compound. The compositions used can also be in various forms. These include solid, semi-solid, and liquid dosage forms, such as tablets, pills, powders, liquid solutions or suspensions, suppositories, injectable and infusible solutions, and sprays. The preferred form depends on the intended method of administration and therapeutic application. The compositions also preferably contain conventional pharmaceutically acceptable carriers and diluents well known to those skilled in the art. Examples of carriers or diluents for use with the compounds include ethanol, dimethyl sulfoxide, glycerol, alumina, starch, saline, and equivalent carriers and diluents. To provide for administration of such dosages for the desired therapeutic treatment, the compositions disclosed herein may advantageously contain from about 0.1% to 100% by weight of the total of one or more subject compounds, based on the weight of the total composition including any carriers or diluents.

[0148] Suitable formulations for administration include, for example, aqueous sterile injection solutions, which may contain antioxidants, buffers, bacteriostatic agents, and solutes that render the formulation isotonic with the blood of the intended recipient; and aqueous and non-aqueous sterile suspensions, including suspending agents and thickening agents. The formulations can be provided in unit-dose or multi-dose containers, such as sealed ampoules and vials, and can be stored in a sterile liquid carrier, for example, a lyophilized (freeze-dried) state, requiring only water for injection prior to use. Extemporaneous injection solutions and suspensions can be prepared from sterile powders, granules, tablets, etc. In addition to the ingredients specifically mentioned above, it should be understood that the compositions disclosed herein may contain other agents conventional in the art, taking into account the type of formulation in question.

[0149] The compounds disclosed herein and compositions comprising them can be delivered to cells through direct contact with cells or via carrier means.Carrier means for delivering compounds and compositions to cells are well known in the art, including, for example, encapsulating the composition in a liposome moiety.Other means for delivering the compounds and compositions disclosed herein to cells include attaching the compound to a protein or nucleic acid that is targeted for delivery to the target cell.U.S. Patent No. 6,960,648 and U.S. Patent Application Publication Nos. 2003 / 0032594 and 2002 / 0120100 disclose amino acid sequences that can be linked to another composition, allowing the composition to translocate across a biological membrane.U.S. Patent Application Publication No. 20020035243 also describes a composition for transporting biological moieties across a cell membrane for intracellular delivery. The compounds can also be incorporated into polymers, examples of which include poly(DL lactide-co-glycolide) polymer for intracranial tumors; poly[bis(p-carboxyphenoxy)propane:sebacic acid], molar ratio 20:80 (as used in GLIADEL); chondroitin; chitin, and chitosan.

[0150] The compounds and compositions disclosed herein, including their pharmaceutically acceptable salts or prodrugs, can be administered intravenously, intramuscularly, or intraperitoneally by infusion or injection.The solution of this active agent or its salt can be prepared in water, optionally mixed with a non-toxic surfactant.Dispersions can also be prepared in glycerol, liquid polyethylene glycol, triacetin, and their mixtures, and in oil.Under normal storage and use conditions, these preparations can contain preservatives to prevent the growth of microorganisms.

[0151] Pharmaceutical dosage forms suitable for injection or infusion include sterile aqueous solutions or dispersions or sterile powders containing the active ingredient, which are suitable for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes. The final dosage form must be sterile, fluid, and stable under the conditions of manufacture and storage. The liquid carrier or vehicle can be a solvent or liquid dispersion medium containing, for example, water, ethanol, polyols (e.g., glycerol, propylene glycol, liquid polyethylene glycol, etc.), vegetable oils, non-toxic glyceryl esters, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions, or by the use of surfactants. If necessary, the prevention of microbial activity can be achieved by various other antibacterial and antifungal agents, such as parabens, chlorobutanol, phenol, sorbic acid, thimerosal, etc. In many cases, it is preferable to include isotonic agents, such as sugars, buffers, or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the inclusion of agents which delay absorption, for example, aluminum monostearate and gelatin.

[0152] Sterile injectable solutions are prepared by incorporating the compounds and / or agents disclosed herein in the required amount in an appropriate solvent with various other ingredients as enumerated above, followed by filter sterilization, as required. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying techniques, which yield a powder of the active ingredient plus any additional desired ingredient present in a previously sterile-filtered solution.

[0153] Useful dosages of the compounds and agents and pharmaceutical compositions disclosed herein can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known in the art.

[0154] The dosage range for administering the composition is large enough to produce the desired effect that the symptom or disorder is affected.The dosage should not be so large as to cause harmful side effects, such as undesirable cross-reaction, anaphylactic reaction, etc. Generally, the dosage varies according to the age, condition, sex and degree of disease of the patient, and can be determined by those skilled in the art.The dosage can be adjusted by an individual physician if any contraindications occur.The dosage can vary and can be administered in one or more daily administrations for one or several days.

[0155] Pharmaceutical compositions comprising the compounds disclosed herein in combination with a pharmaceutically acceptable carrier are also disclosed. Pharmaceutical compositions suitable for oral, topical, or parenteral administration contain an amount of the compound constituting a preferred embodiment. The dose administered to a patient, particularly a human, should be sufficient to achieve a therapeutic effect in the patient over a reasonable time frame without lethal toxicity and, preferably, without causing unacceptable side effects or morbidity. Those skilled in the art will recognize that the dose will depend on various factors, including the subject's condition (health), the subject's weight, the type of concurrent treatment, if any, the frequency of treatment, the therapeutic ratio, and the severity and stage of the pathological condition.

[0156] Also disclosed are kits comprising a compound disclosed herein in one or more containers. The disclosed kits may optionally include a pharmaceutically acceptable carrier and / or diluent. In one embodiment, the kit includes one or more other components, additives, or adjuvants as described herein. In another embodiment, the kit includes one or more anticancer agents, such as the agents described herein. In one embodiment, the kit includes instructions or packaging that explain how to administer the compound or composition of the kit. The containers of the kit can be made of any suitable material, such as glass, plastic, metal, etc., and of any suitable size, shape, or configuration. In one embodiment, the compound and / or agent disclosed herein is provided in the kit in solid form, such as a tablet, pill, or powder. In another embodiment, the compound and / or agent disclosed herein is provided in the kit as a liquid or solution. In one embodiment, the kit includes an ampoule or syringe containing the compound and / or agent disclosed herein in liquid or solution form.

[0157] Although several embodiments of the present invention have been described, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.

[0158] Several publications, patents, and patent applications are cited herein. Each of the cited publications, patents, and patent applications is herein incorporated by reference in its entirety to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference in its entirety. [Example]

[0159] Example 1 Design Strategy and Synthesis of Cyclic CPP-Stapled Peptide Conjugates We chose to prepare cCPP-stapled peptide conjugates using a convergent synthesis method (Figure 1). First, a cargo peptide was synthesized by standard solid-phase peptide synthesis (SPPS) incorporating two homocysteine ​​residues at the i and i+4 positions. After cleavage from the resin and side-chain deprotection, the peptide was treated with 1.5 equivalents of 1,3-dichloroacetone (DCA) to staple the peptide into an α-helical conformation. This stapling procedure also incorporates a ketone group into the stapled peptide for subsequent bioorthogonal conjugation with the cCPP. Next, a cCPP [e.g., CPP9] was synthesized by SPPS, and a miniPEG-Lys(Mtt) linker was attached to the Gln side chain. While still on the resin, the Mtt group on the Lys side chain was selectively removed by treatment with 5% trifluoroacetic acid (TFA), and the exposed amine was then acylated with a Boc-aminoxyacetyl moiety. Cleavage from the resin and deprotection of the side chain with TFA yielded CPP9 derivatized with a nucleophilic hydroxylamine group (aminoxy-CPP9; Figure 1). Finally, the DCA-stapled peptide and aminooxy-CPP9 were conjugated in aqueous solution (pH 4.7) through the formation of an oxyyne bond. Note that the formation of the oxyyne yields two distinct stereoisomers (Z and E isomers).

[0160] Example 2 Stapled peptides around the water parsley on MDM2-p53 interaction As a proof of concept, we synthesized cell-permeable stapled peptides directed against the MDM2-p53 interaction. Activation of the p53 protein protects the organism from proliferation of cells carrying damaged DNA with potentially oncogenic mutations. MDM2, a p53-specific E3 ubiquitin ligase, is the primary cellular antagonist of p53 and acts to limit p53 growth-suppressing function in cancer cells. MDM2 mediates p53 monoubiquitination and proteasomal degradation. Disruption of the p53-MDM2 complex with small molecules and stapled peptides is a common approach to treating cancer with wild-type p53 protein. See Wade, M., et al., Nature Reviews Cancer 13, 83-96 (2013).

[0161] A previously reported MDM2 ligand, Ac-LTFEHYWAQLTS (SEQ ID NO: 1) ("PDI"; see Phan, J., et al., J. Biol. Chem. 285, 2174-2183 (2010)), was selected and labeled with fluorescein isothiocyanate (FITC) at its C-terminus via a miniPEG-Lys linker. This FITC-labeled peptide (Table 5, peptide 1) exhibited a K of 80 nM, similar to the reported value. D For stapling, Glu-4 and Ala-8 or His-5 and Gln-9 were replaced with homocysteine ​​residues, respectively, and the two resulting peptides were stapled with DCA as described above (Table 5, peptides 2 and 3). Peptides 2 and 3 bound to MDM2 with K values ​​of 144 and 171 nM, respectively. D Peptide 2 bound to MDM2 with IC values ​​of 220 and 201 nM. Due to its rather high potency, peptide 2 was selected for conjugation with CPP9 as described above, giving two stereoisomers, peptides 4 and 5, which were then separated by HPLC, although the actual Z / E configuration at the oxime moiety was not determined (Figure 5). The binding affinities of peptides 4 and 5 for MDM2 were determined by examining their ability to compete with FITC-labeled peptide 1 for binding to MDM2 in a fluorescence anisotropy (FA)-based assay. Peptides 4 and 5 had IC values ​​of 220 and 201 nM, respectively. 50values ​​are shown (Table 1), suggesting that binding to CPP9 does not significantly affect stapled peptide binding to MDM2. [Table 8] a miniPEG, 8-amino-3,6-dioxaoctanoic acid; homoC, homocysteine; DCA, 1,3-dichloroacetone. Reported values ​​are the K values ​​for FITC-peptides 1–3. D values ​​and IC of unlabeled peptides 4 and 5 50 value.

[0162] Peptides 4 and 5 were tested for anticancer activity against human colon cancer cell lines harboring wild-type (HCT116 p53+ / +) and mutant p53 genes (HCT116 p53- / -) using an MTT viability assay. Peptides 4 and 5 dose-dependently reduced the viability of wild-type p53 cells, but not p53 mutant cells (Figure 2). As previously reported, Nutlin-3, a small molecule inhibitor of MDM2, selectively killed wild-type p53 cells in a dose-dependent manner. See Vassilev, LT, et al., Science, 303, 844-848 (2004).

[0163] In contrast, the stapled peptide without CPP9 (peptide 2) showed no significant effect on either cell line, presumably due to its inability to penetrate the cell membrane (see below).

[0164] Example 3 Peptide Stapling and Conjugation with 3,5-Bis(bromomethyl)benzoic Acid The main limitation of the oxime-based conjugation method is the formation of two different stereoisomers, which complicates the separation and further clinical development of the product. To overcome this limitation, 3,5-bis(bromomethyl)benzoic acid ("BBA") was then used as the stapling agent. A structurally similar compound, m-xylene dibromide, has previously been used to staple α-helical peptides. See Jo, H., et al., J Am Chem Soc. 134, 17704-17713 (2012). m-xylene dibromide reacts rapidly with two cysteines in close spatial proximity to form a single stapled peptide product with high yield and low reagent / peptide stoichiometry. Two methods for stapling / conjugating α-helical peptides using BBA were developed. In the first method (Figure 3A), a cargo peptide containing two acetamidoethyl (Acm)-protected cysteines is first synthesized on a solid support by standard solid-phase peptide synthesis (SPPS). The Acm groups are removed with Hg(OAc)2, and the exposed free thiol is alkylated with BBA. While on the resin, the benzoic acid group reacts with an N-Fmoc-1,3-diaminopropane linker in the presence of a coupling agent (e.g., HATU) to generate an amine moiety, which serves as a handle in the subsequent synthesis of β-Ala-CPP9 by SPPS.

[0165] In the second method (Figure 3B), CPP9 is synthesized on solid phase using a miniPEG-Lys(Mtt) linker. The Mtt group on the lysine side chain is selectively removed with 5% TFA, and the exposed amine is linked to BBA using HATU as a coupling agent. Cleavage from the resin and deprotection of the side chain with TFA, followed by HPLC purification, yields BBA-derivatized CPP9, which can be conjugated to a fully deprotected cysteine-containing peptide simply by mixing the two peptides in neutral aqueous solution.

[0166] The advantage of the first method is that the entire CPP-staple peptide conjugate can be synthesized on solid phase and the product only needs to be purified once, whereas the second method is modular and convergent and can be applied to rapidly generate a large number of different CPP / cargo combinations for testing to identify the optimal CPP-cargo conjugate.

[0167] Example 4 CPP9 confers consistent cell permeability to stapled peptides. We applied the stapling / conjugation method (Figure 3B) to Ac-LTFEHYWAQLTS (SEQ ID NO: 1) ("PDI"), a known MDM2 ligand. See Hu, B., et al., Cancer Res. 67, 8810-8817 (2007). The Glu-4 and Ala-8 residues were replaced with cysteine ​​(peptides 6 and 7) or homocysteine ​​(peptides 8 and 9), and the resulting peptides were stapled with BBA and conjugated to CPP9 (Table 2, peptides 7 and 9). As a control (without CPP), the peptides were stapled with m-xylene dibromide to obtain neutral hydrophobic staples (peptides 6 and 8). The cytosolic translocation efficiency of the peptides was assessed by C-terminal labeling with 5(6)-carboxynaphthofluorescein (NF) via a flexible miniPEG-Lys linker and then quantifying intracellular fluorescence by flow cytometry. With a pKa of 7.8, NF fluoresces in the neutral environment of its cytosol and nucleus (pH 7.4), but is minimally fluorescent in acidic endosomes / lysosomes (pH ≤ 6.0). As expected, both CPP9-conjugated peptides (peptides 7 and 9) are highly cell-permeable, with cytosolic translocation efficiencies of 497% and 30%, respectively, compared to CPP9 (100%), making it one of the most effective CPPs reported to date. Unfortunately, the solubility of unconjugated peptides 6 and 8 was too low to reliably measure their cellular uptake efficiencies. To increase aqueous solubility, the N-terminal leucine of peptide 6 was replaced with glutamic acid to yield peptide 10. A second glutamic acid residue was then added to the N-terminus of peptide 10 to generate peptide 12 (Table 6). Conjugation of peptides 10 and 12 with CPP9 yielded peptides 11 and 13, respectively. Remarkably, treatment of HeLa cells with 5 μl of peptide 10 or 12 (without CPP) for 2 h at 37°C resulted in minimal cellular uptake (2.8% for both), whereas conjugation of the peptide with CPP9 increased the cytosolic translocation efficiency by 48- and 86-fold, respectively (Table 6 , peptides 11 and 13).

[0168] To test whether this dramatic improvement in cell permeability is generalized to other stapled peptides, we synthesized four additional pairs of stapled peptides, with and without conjugation to CPP9, and compared their cytosolic translocation efficiencies (Table 6, peptides 14–21). After analyzing over 200 stapled peptides, Verdine and colleagues previously reported peptide 14 as one of the most cell-permeable stapled peptides, whereas peptides 16, 18, and 20 were the least permeable. See Chu, Q., Med. Chem. Commun. 6, 111–119 (2015). Consistent with Verdine's findings, xylene-stapled peptide 14 (without CPP) exhibited superior cell permeability (47% of that of CPP9), whereas peptides 16 and 18 did not (2.5% and 8.9%, respectively). Due to its limited solubility, the cytosolic translocation efficiency of peptide 20 could not be measured. Again, after conjugation with CPP9, all four peptides (15, 17, 19, and 21) exhibited high cell permeability, showing an 11- to 152-fold improvement over their unconjugated counterparts. The variation in cell permeability among CPP9-conjugated peptides (30-508%) is likely caused, at least in part, by differential binding to serum proteins (all flow cytometry experiments in this work were performed in the presence of 10% fetal bovine serum). In general, hydrophobic cargoes tend to bind to serum proteins and / or aggregate, which results in significantly reduced cellular uptake efficiency.

[0169] Four pairs of peptides in Table 6 were also labeled with FITC, and their translocation into HeLa cells was monitored by live-cell confocal microscopy (Figure 4). In all four cases, the stapled peptide alone (without CPP) showed minimal uptake, whereas the CPP9-peptide conjugates efficiently translocated into cells. Consistent with the flow cytometry data, diffuse fluorescence was present throughout the cell, indicating that a significant proportion of the internalized peptide escaped from endosomes into the cytosol and nucleus. Taken together, our data suggest that conjugation to a cCPP (such as CPP9) can confer high and consistent cell permeability to stapled peptides. [Table 9] a ΦΦ, L-2-naphthylalanine; βΑ, beta-alanine; r, D-arginine; NF, 5(6)-carboxynaphthofluorescein; hC, homocysteine; BBA, 3,5-dimethylbenzoyl; miniPEG, 8-amino-3,6-dioxaoctanoic acid b All reported values ​​are relative to the value for CPP9, which is defined as 100%. ND, not determined due to limited aqueous solubility.

[0170] Example 5 Biochemical and Biological Activities of Stapled Peptides Peptides 6–13, mutants of the MDM2 ligand PDI, were tested for binding to MDM2. Substitution of Glu-4 and Ala-8 residues with cysteine ​​and stapling with BBA reduced MDM2 binding affinity by approximately 2.5-fold (K for peptides 1 and 6, respectively). D = 80 and 190 nM). Conjugation with CPP9 further reduced the MDM2 binding affinity by approximately 2-fold (K = 80 and 190 nM for peptide 7). D 300 nM) (Table 7). Substitution of Glu-4 and Ala-8 with homocysteine ​​followed by BBA stapling improved MDM2 binding affinity by 5-fold (K for peptide 8). D=14 nM), but further conjugation with CPP9 reduced the affinity by approximately 8-fold (K D =114 nM). Substitution of Leu-1 with Glu resulted in a 5-fold increase in the binding affinity of peptide 6 (K = 114 nM for peptide 10). D = 36 nM), likely due to electrostatic interactions with the positively charged MDM2 surface near the N-terminus of the peptide ligand. Again, binding to CPP9 reduced MDM2 binding affinity by 6-fold (K = 36 nM for peptide 11). D = 225 nM). However, adding a second Glu to the N-terminus of peptide 11 did not further improve the binding affinity (K = 225 nM for peptide 13). D =365nM). [Table 10] a hC, homocysteine; BBA, 3,5-dimethylbenzoyl; miniPEG, 8-amino-3,6-dioxaoctanoic acid.

[0171] Example 6 Cytosolic Delivery of Stapled Peptides Conjugated to Various Peptide Transduction Domains (PTDs) A series of stapled peptide conjugates were evaluated to compare the ability of various peptide transduction domains (PTDs) to affect cytosolic delivery of the stapled MDM2 inhibitor sPDI (Figures 20A-20D). Structure 22 shows that the PDI sequence is stapled via an amide group formed between an aspartic acid and a lysine residue. Each conjugate (Figures 20B-20D) further contains a C-terminal linker attached to either CPP9 (Structure 23), R9 (Structure 24), or Tat (Structure 25).

[0172] To evaluate the delivery suitability of each conjugate, peptides 22–25 were labeled with FITC, and their translocation into HeLa cells was monitored by live-cell confocal microscopy (Figure 21). HeLa cells were treated with 5 μl of FITC-labeled peptide for 2 hours at 37°C and washed to remove excess peptide. Images obtained after treatment showed that the stapled peptide alone (structure 22) showed minimal uptake, whereas the conjugates translocated to various degrees into the cells. The most effective conjugate for delivering sPDI was CPP9-conjugated peptide 23. R9 and Tat were also able to deliver the MDM2 inhibitor to the cytosol, although with significantly reduced efficiency. Again, these data suggest that conjugation to a cCPP (such as CPP9) can confer high and consistent cell permeability to stapled peptides.

[0173] Example 7 Functional Delivery of Stapled MDM2 Inhibitor sPDI Conjugated to CPP9 Using cell-free antagonism experiments measuring fluorescence polarization, we determined how effectively CPP9 could target and deliver a stapled MDM2 inhibitor. In this study, sPDI had an IC of 98.4 nM. 50 CPP9-sPDI effectively inhibited MDM2 as a function of competitor peptide concentration at 1000 rpm. CPP9-sPDI also acted as an effective inhibitor, with an IC of 63.3 nM. 50 The CPP9-sPDI mutant exhibits improved activity. Without being bound by any particular theory, for conjugation to be effective, the sPDI peptide must reach MDM2 without interference from other moieties. This result indicates that CPP9-sPDI is structured such that the interaction between sPDI and MDM2 is not impeded. This is not the case for the F10A mutant, which has substantially reduced activity—a finding that confirms the importance of peptide sequence for MDM2 inhibition.

[0174] Example 8 Evaluation of the antiproliferative effect of CPPS9-sPDI Additionally, the antiproliferative effect of CPP9-sPDI (Structure 23) was evaluated. Figure 23 compares the effects of CPP9-sPDI, Nutlin-3a, R9-sPDI, sPDI, CPP9-sPDI(F10A), and Tat-sPDI (0-20 μM) on the viability of the SJSA-1 cell line after 72 hours of treatment in the presence of 10% FBS, as measured by MTT assay. Compared to the known MDM2 inhibitor Nutlin-3a, CPP9-sPDI exhibited an IC of 3.86 μM. 50 The F10A peptide variant resulted in a more than five-fold reduction in cytotoxicity compared to CPP9-sPDT; this result reinforces that MDM2 is inhibited by sPDI but not by CPP9 or its fragments. Notably, this peptide exhibited comparable efficacy to CPP9-sPDI in cell-free binding assays, yet sPDI possessed substantially reduced cytotoxicity (Figure 22).

[0175] The mechanism of action (MOA) of CPP9-sPDI was also considered during cytosolic delivery of the MDM2 inhibitor. + / Propidium iodide + (PI + Using a flow cytometry assay to detect SJSA-1 cells, we demonstrate that the antiproliferative activity of CPP9-SPDI is mediated by the apoptotic pathway. This behavior is similar to that of Nutiin-3a, which is known to induce p53-dependent apoptosis in certain cancer cell lines. In this study, we measured the percentage of Annexin V+ / PI+ and Annexin V+ / PI- SJSA-1 cells after 48 hours of treatment with the inhibitor in the presence of 10% FBS.

[0176] The serum stability of CPP9-sPDI was assessed by incubating the conjugate in 25% human serum at 37°C for 24 hours. Figure 25 shows that CPP9-sPDI steadily decreased over this period, such that 25% of the compound was detected at the end of the study. This observed level of serum stability (cargo region) was consistent with the IC measured for this compound. 50 may affect the value.

[0177] Experiment details Peptide synthesis and labeling. Peptides were manually synthesized by SPPS on Rink amide resin using Fmoc chemistry and 2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) as the coupling agent. The coupling reaction typically involved 5 equivalents of Fmoc-amino acid, 5 equivalents of HATU, and 10 equivalents of diisopropylethylamine (DIPEA) and was carried out at room temperature for 45 minutes. The peptides were cleaved from the resin and deprotected by treatment with 92.5% TFA, 2.5% water, 2.5% triisopropylsilane, and 2.5% 1,3-dimethoxybenzene for 3 hours at room temperature. The solvent was removed by passing a stream of N2 over the solution, and the residue was then triturated with cold diethyl ether. The crude peptides were collected by C column eluted with a linear gradient of acetonitrile (containing 0.05% TFA) in ddHO (containing 0.05% TFA). 18 The peptides were purified by reverse-phase HPLC with a column. Fluorescent labeling of the peptides was performed in the liquid phase. Lyophilized peptides were incubated with 5 equivalents of activated fluorescent labeling reagent (e.g., fluorescein isothiocyanate or 5(6)-carboxynaphthofluorescein succinimidyl ester) and 5 equivalents of DIPEA in DMF for 2 hours. The reaction was quenched with TFA, and the labeled peptides were then purified again by HPLC, and their authenticity was confirmed by MALDI-TOF mass spectrometry.

[0178] Peptide stapling with DCA. Cysteine-containing peptides were dissolved in 1 mL of DMF containing 100 mM NH4HCO3 (pH = 8.1) and 1.1 equivalents of tris(2-carboxyethyl)phosphine (TCEP) to a peptide concentration of approximately 0.1 mM. The solution was incubated at room temperature for 1 hour with mixing on a rotary shaker. Then, 1.5 equivalents of dichloroacetone in DMF were added to the mixture, and the solution was incubated at room temperature for 3 hours (with mixing). The reaction products were purified by reverse-phase HPLC and analyzed by MALDI-TOF MS.

[0179] Synthesis of Aminoxy-CPP9 CPP9 was synthesized by standard SPPS and a miniPEG-Ne-4-methoxytrityl-L-lysine moiety was added to the C-terminus. While still on the resin, the Mtt group on the lysine side chain was selectively removed by treatment with 2% (v / v) TFA in DCM for 1 hour. The resin was then incubated with 5 equivalents of (Boc-aminoxy)acetic acid, 5 equivalents of diisopropylcarbodiimide (DIC), and 5 equivalents of HOBT in DCM / DMF (1:1 v / v) for 1 hour (twice). The resulting aminoxy-CPP9 peptide was cleaved from the resin, purified by HPLC, and analyzed by MALDI-TOF MS as previously described.

[0180] Synthesis of CPP9-stapled peptide conjugates via oxime formation DCA-staple peptide (0.5 mM) was dissolved in 10 mL of 100 mM NHOAc solution (pH 4.5) containing 100 mM aniline. Aminoxy-CPP9 (2.0 equiv.) was added to the solution, and the mixture was incubated overnight at room temperature with mixing. The reaction product was purified by reverse-phase HPLC using a C18 column eluted with a linear gradient of 10–60% acetonitrile in ddHO (containing 0.05% TFA). The authenticity of the reaction product was confirmed by MALDI-TOF MS (see, for example, Figure S1).

[0181] Expression and purification of GST-MDM2 E. coli BL21(DE3) cells were transformed with the prokaryotic vector pGEX-6P-2, encoding the human MDM2 gene (residues 17-125). Cells were grown in L broth supplemented with 100 μg / mL ampicillin at 37°C to an OD600 of 0.6, and then protein expression was induced by the addition of 1 mM IPTG at 30°C for 5 hours. Cells were pelleted by centrifugation at 2,000 rpm for 30 minutes. The cell pellet was resuspended in 50 mL of lysis buffer (50 mM Tris-HCl, pH 7.4, 300 mM NaCl, 2.5 mM EDTA, 0.02% NaN3, and 2 mM DTT) and lysed by sonication on ice. The lysate was centrifuged at 15,000 rpm for 30 minutes in an SS-34 fixed-angle rotor. The supernatant was loaded onto a glutathione-Sepharose column, and bound proteins were eluted with lysis buffer containing 10 mM GSH.

[0182] MTT assay HCT116 p53 wild-type and HCT116 p53 - / - Cells were plated in 96-well plates at 3x10 3 Cells were seeded at 1000 kJ / well and grown overnight. Different concentrations (0-12.5 μM) of peptide were added to the cells in McCoy's 5A medium supplemented with 10% FBS and 1% penicillin / streptomycin and incubated at 37°C for 48 hours in the presence of 5% CO2. Then, 10 μL of MTT stock solution (5 mg / mL) was added to each well, and the plate was incubated at 37°C for 4 hours. 100 μL of SDS-HCl solubilization solution was added, and the plate was incubated at 37°C overnight. The absorbance of the formed formazan product was measured at 570 nm on a Tecan microtiter plate reader.

[0183] Flow cytometry HeLa cells were plated at 1.5x10 in a 12-well plate. 5Cells / well were seeded for 24 hours. The next day, naphthofluorescein-labeled peptides (5 μM) were added to cells in DMEM medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin / streptomycin. The cells were then incubated at 37°C for 2 hours in the presence of 5% CO2. The peptide-containing medium was removed, and the cells were washed twice with DPBS. The cells were detached from the plate using 0.25% trypsin, pelleted by centrifugation at 250 g for 5 minutes, washed twice with DPBS, resuspended in DPBS, and analyzed on a BD FACS LSR II or Aria III flow cytometer. For NF-labeled peptides, a 633-nm laser was used for excitation, and the fluorescence emission was analyzed in the APC channel. Data were analyzed using Flowjo software (Tree Star).

Claims

1. A polypeptide conjugate comprising a cyclic cell-penetrating peptide (cCPP) and a stapled peptide having the structure of Formula IA or IB below. 【Chemistry 1】 (In the formula, Staple peptides are U, Y １ , Y ２ , X, Z, J, Z′ or a combination thereof and a staple, and at least one region having an α-helical structure; each of X and Z, at each occurrence, is independently an amino acid; U is independently in each occurrence and when present, an amino acid; J is independently in each occurrence and when present, an amino acid; Z' is independently in each occurrence and when present, an amino acid; a is a number between 0 and 500, c is 3, 6, or 10; d is a number between 1 and 500, e is a number between 0 and 500, each of g and h is independently, at each occurrence, 0 or 1, with the proviso that in Formula IA, g is 0 or 1, and in Formula IB, either g or h is 1; i is a number between 0 and 100, Y １ is a first binding group (b １ ), Y ２ is a second binding group (b ２ ), cCCP is a cyclic peptide comprising about 4 to about 13 amino acids, said about 4 to about 13 amino acids comprising at least two arginines and at least two amino acids having hydrophobic side chains; The staple comprises an alkylene or an aryl, each of which is optionally substituted; The linker has the structure L-1 or L-2: 【Chemistry 2】 [AA ｓ is the side chain or terminus of an amino acid on a peptide or staple; A.A. ｃ is the side chain or terminus of an amino acid of cCPP; p is an integer from 0 to 10; and q is an integer from 1 to 50. and Each of b1 and b2 is independently absent or a thioether.

2. 2. The polypeptide conjugate of claim 1, wherein the cCPP has a sequence comprising any of Formula IIIA to Formula IIID. 【Transformation 3】 (In the formula, A.A. Ｈ１ and A.A. Ｈ２ each of is independently a D hydrophobic amino acid or an L hydrophobic amino acid; In each case and if present, AA Ｕ and A.A. Ｚ are each independently a D or L amino acid; m and n are independently any number from 0 to 6.

3. The polypeptide conjugate of claim 1, wherein the staple comprises an alkylene or aryl substituted with oxo or N-oxide.

4. The polypeptide conjugate of any one of claims 1 to 3, wherein the polypeptide conjugate of formula IB is represented by the following structure: 【Chemistry 4】

5. (i) J is absent and Z may be at either the N-terminus or the C-terminus of the stapled peptide; (ii) J is present, e is 1, and J may be at either the N-terminus or the C-terminus of the stapled peptide; or (iii) J is present, e is 2 or greater, and the terminal J is either the N-terminus or the C-terminus of the stapled peptide.

6. (i) U is absent and Z' is either the N-terminus or the C-terminus of the stapled peptide; (ii) U is present, a is 1, and U is either the N-terminus or the C-terminus of the stapled peptide; or The polypeptide conjugate of any one of claims 1 to 5, wherein (iii) U is present, a is 2 or greater, and the terminal U is at either the N-terminus or C-terminus of the stapled peptide.

7. A cell comprising the polypeptide conjugate of any one of claims 1 to 6.

8. A method for cellular delivery of a stapled peptide, comprising contacting a cell with a polypeptide conjugate according to any one of claims 1 to 6.

9. A pharmaceutical composition comprising the polypeptide conjugate of any one of claims 1 to 6.

10. A pharmaceutical composition comprising the polypeptide conjugate of any one of claims 1 to 6 for treating a disease or condition selected from cancer, an inflammatory disease or condition, and an autoimmune disease or condition.

11. A method for producing the polypeptide conjugate of any one of claims 1 to 6, comprising conjugating a stapled peptide and a cCPP.

12. A method for producing a polypeptide conjugate according to any one of claims 1 to 6, comprising conjugating a peptide to at least one cCPP and immobilising said peptide.

13. 2. The polypeptide conjugate of claim 1, comprising peptide 4, peptide 11, peptide 13, peptide 15, peptide 17, peptide 19, or peptide 21. Peptide 4 【Transformation 5】 Peptide 11 【Transformation 6】 Peptide 13 【Transformation 7】 Peptide 15 【Transformation 8】 Peptide 17 【Chemistry 9】 Peptide 19 【Chemistry 10】 Peptide 21 【Chemistry 11】

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