发明名称 Peptides that inhibit the interaction between ASF1 and histones, and use thereof
摘要 The present invention relates to peptides capable of inhibiting the formation of the complex between the Asf1 histone chaperone and histones H3-H4, and to the use thereof as a drug, particularly for treating cancer.
申请公布号 US9526757(B2) 申请公布日期 2016.12.27
申请号 US201214358875 申请日期 2012.11.16
申请人 COMMISSARIAT A L'ENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES;UNIVERSITE PIERRE ET MARIE CURIE (PARIS VI) 发明人 Ochsenbein Francoise;Guerois Raphael;Gaubert Albane;Courbeyrette Regis
分类号 A61K38/16;A61K38/00;A61K38/10;A61K38/04;C07K5/00;C07K7/00;C07K16/00;C07K17/00;A61K38/03;C07K14/00;C07K14/47 主分类号 A61K38/16
代理机构 Saliwanchik, Lloyd & Eisenschenk 代理人 Saliwanchik, Lloyd & Eisenschenk
主权项 1. A peptide comprising elements E1-B-E2, wherein: a) E1 is a peptide characterized by the sequence of formula (I) X1-X2-X3-X4-X5-K-X6-X7-X8-L-X9-X10-R-I-X11  (I) wherein the peptide of formula (I) is either: i) SEQ ID NO: 1 wherein X1 and X2 are absent; X3 is an amino acid selected from the group consisting of A, C, V, P, L, I, M, F, W, R and Y; X4 is an amino acid selected from the group consisting of T, S, P, D, M and N; X5 is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; X6 is an amino acid selected from the group consisting of Q, E, L, M, A, D, and W; X7, X8 and X9, independently of each other, are an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y, provided that at least two of the residues X7, X8 and X9 are an amino acid selected from the group consisting of A, R, D, N, C, G, Q, E, H, L, K, M, F, S, W and Y; and X10 and X11, independently of each other, are an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; or ii) SEQ ID NO: 2 wherein X1 is absent or is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; X2 is absent or is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; X3 is an amino acid selected from the group consisting of T, S, P, D and N; X4 and X5, independently of each other, are an amino acid selected from the group consisting of A, R, D, N, C, G, Q, E, H, L, K, M, F, S, W and Y; X6 is an amino acid selected from the group consisting of Q, E, L, M, A, D and W; X7, X8 and X9, independently of each other, are an amino acid selected from the amino acids A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y, provided that at least two of the residues X7, X8 and X9 are an amino acid selected from the group consisting of A, R, D, N, C, G, Q, E, H, L, K, M, F, S, W and Y; and X10 and X11, independently of each other, are an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; b) B is a peptide characterized by the sequence of formula (II) G-X12-G-X13-X14  (II) (SEQ ID NO: 3) wherein: X12 is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; X13 is absent or selected from the amino acids G, A and S; and X14 is absent or is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; and c) E2 is a peptide characterized by the sequence of formula (III) X15-X16-X17-X18-G-X19-X20  (III) (SEQ ID NO: 4) wherein: X15 is an amino acid selected from A, R, D, N, C, G, Q, H, I, L, K, M, F, P, S, T, V, W and Y; X16 is T or V; X17 is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y; X18 is an amino acid selected from the group consisting of A, D, N, C, G, Q, E, H, I, L, M, F, P, S, T, V, W and Y; X19 is an amino acid selected from the group consisting of A, C, V, P, L, I, M, F, W and Y; and X20 is absent or is an amino acid selected from A, R, D, N, C, G, Q, E, H, I, L, K, M, F, P, S, T, V, W and Y.
地址 Paris FR
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