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    • 5. 发明申请
    • STABLE CELL BINDING CHIMERIC PEPTIDES
    • 稳定细胞结合重组肽
    • WO2009128077A1
    • 2009-10-22
    • PCT/IL2009/000420
    • 2009-04-16
    • HADASIT MEDICAL RESEARCH SERVICES AND DEVELOPMENT LTD.GORODETSKY, Raphael
    • GORODETSKY, Raphael
    • C07K14/75A61K38/36A61L27/22C12N15/62
    • C07K14/75A61K38/00A61L27/22C07K14/515C07K14/78C07K2319/00C12N15/62
    • The present invention relates to novel family of homologous cell attachment chimeric peptides. In particular, the present invention relates to chimeric peptides, each comprising synthetic peptides comprising (a) an M-tide comprising an amino acid sequence that is at least 80% homologous to the amino acid sequence selected from the group consisting of: SEQ ID NO:1, 2 and 37; and (b) a core haptide comprising an amino acid sequence homologous to amino acid sequences at the carboxy termini of the and E chains of fibrinogen or other proteins comprising C-termini that are homologous to said fibrinogen sequences, wherein the M-tide and the core haptide originate from the same protein. The synthetic peptides are linked to one another thereby providing the chimeric peptides of the invention which does not occur in the native protein as a continuous sequence. The present invention further discloses pharmaceutical compositions comprising said chimeric peptides and uses thereof.
    • 本发明涉及同源细胞附着嵌合肽的新家族。 特别地,本发明涉及嵌合肽,每个嵌合肽包含合成肽,其包含(a)含有与选自以下的氨基酸序列至少80%同源的氨基酸序列的M潮流:SEQ ID NO 1:2和37; 和(b)核心浸液,其包含与纤维蛋白原的E链的羧基末端的氨基酸序列同源的氨基酸序列或包含与所述纤维蛋白原序列同源的C末端的其它蛋白质,其中M潮和 核心浸液源自相同的蛋白质。 合成肽彼此连接,由此提供本发明的嵌合肽,其不以天然蛋白质的形式存在,作为连续序列。 本发明还公开了包含所述嵌合肽及其用途的药物组合物。
    • 9. 发明申请
    • NOVEL HAPTOTACTIC PEPTIDES
    • 新颖的皮肤病
    • WO0153324A2
    • 2001-07-26
    • PCT/IL0100057
    • 2001-01-21
    • HADASIT MED RES SERVICEMARX GERARDGORODETSKY RAPHAEL
    • MARX GERARDGORODETSKY RAPHAEL
    • C12N15/09A61K35/12A61K38/00A61K38/36A61K45/00A61K47/48A61K49/00A61K51/00A61L27/00A61P9/00A61P17/02A61P19/08C07K14/75C07K16/36C07K
    • A61K38/363C07K14/75
    • Novel peptide sequences homologous to the known fibrinogen derived haptotactic peptides, C beta and C alpha E, are disclosed. The novel peptides are derived from proteins related or unrelated to fibrinogen including a peptide adjacent to fibrinogen gamma -chain C terminus denoted pre-C gamma as well as isotypes of angiopoietin, human microfibril-associated glycoprotein (mfap) and tenascins. Novel peptides having significant homology to the known fibrinogen derived haptotactic peptides are now shown to possess cell attraction activities. Active fragments comprising shorter 8-10 mer peptides are also disclosed, and shown to elicit significant haptotactic activity from a variety of cells, such as fibroblasts, endothelial and smooth muscle cells. The homologous peptides disclosed permit delineation of consensus sequences for haptotactic activity. The peptides are useful in pharmaceutical compositions alone or in conjunction with a medical device or implant.
    • 公开了与已知的纤维蛋白源衍生的触角肽Cβ和CαE同源的新型肽序列。 新型肽衍生自与纤维蛋白原相关或不相关的蛋白质,包括与纤维蛋白原γ链C端相邻的肽,表示为前Cγ,以及血管生成素,人微纤维相关糖蛋白(mfap)和腱生蛋白的同种型。 与已知的纤维蛋白原衍生的结合肽具有显着同源性的新肽现在显示具有细胞吸引活性。 还公开了包含较短的8-10个mer肽的活性片段,并且显示出从各种细胞如成纤维细胞,内皮细胞和平滑肌细胞引起显着的结合活性。 所公开的同源肽允许描述触发活性的共有序列。 肽可单独或与医疗装置或植入物一起用于药物组合物中。