首页> 外国专利> Composition of matter, nucleic acid, expression vector, host cell, process for preparing a pth / pthrp receptor antagonist, and method of treating osteopenia

Composition of matter, nucleic acid, expression vector, host cell, process for preparing a pth / pthrp receptor antagonist, and method of treating osteopenia

机译:物质组成,核酸,表达载体,宿主细胞,制备pth / pthrp受体拮抗剂的方法以及治疗骨质减少的方法

摘要

"MATTER COMPOSITION, NUCLEIC ACID, EXPRESSION VECTOR, HOST CELL, PROCESS FOR PREPARING A PTH / PTHRP RECEIVER ANTAGONIST, AND METHOD OF TREATING OSTEOPENIA". The present invention relates to therapeutic agents that modulate PTH and PTHrP activity. In accordance with the present invention, PTH and PTHrP modulators comprise: (a) a PTH / PTHrP modulator domain; and (b) a carrier, such as a polymer (e.g. PEG or dextran) or an Fc domain, which is preferred: wherein the carrier is covalently linked to the C-terminus of the PTH / PTHrP modulator domain. The vehicle and the PTH / THrP modulating domain may be linked through the N or C terminus of the PTH / THrP modulating domain as described below. The preferred vehicle is an Fc domain and the preferred Fc domain is an IgG Fc domain. Preferred PTH / PTHrP modulator domains include the PTH and PTHrP derived amino acid sequences described below. Other PTH / PTHrP modulating domains may be generated by phage demonstration, RNA-peptide screening and other techniques mentioned herein. Such peptides will typically be modulators of both PTH activity and PTHrP activity, although such techniques may be used to generate peptide sequences that serve as selective modulators (eg, agonists of PTH activity but not PTHrP activity).
机译:“物质组成,核酸,表达载体,宿主细胞,PTH / PTHRP受体拮抗剂的制备方法以及治疗骨质疏松症的方法”。本发明涉及调节PTH和PTHrP活性的治疗剂。根据本发明,PTH和PTHrP调节剂包括:(a)PTH / PTHrP调节剂域; (b)载体,例如聚合物(例如PEG或葡聚糖)或Fc结构域,其是优选的:其中所述载体共价连接至PTH / PTHrP调节剂结构域的C-末端。载体和PTH / THrP调节域可以通过PTH / THrP调节域的N或C末端连接,如下所述。优选的载体是Fc结构域,并且优选的Fc结构域是IgG Fc结构域。优选的PTH / PTHrP调节剂结构域包括下述的PTH和PTHrP衍生的氨基酸序列。其他PTH / PTHrP调节域可以通过噬菌体展示,RNA-肽筛选和本文提及的其他技术来产生。此类肽通常将是PTH活性和PTHrP活性的调节剂,尽管此类技术可用于生成用作选择性调节剂的肽序列(例如,PTH活性而不是PTHrP活性的激动剂)。

著录项

  • 公开/公告号BR0110391A

    专利类型

  • 公开/公告日2003-02-25

    原文格式PDF

  • 申请/专利权人 AMGEN INC.;

    申请/专利号BR20010110391

  • 申请日2001-04-27

  • 分类号C07K14/705;

  • 国家 BR

  • 入库时间 2022-08-22 00:03:49

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