发明名称 Use of a latent myostatin complex comprising a myostatin pro-peptide and a myostatin c-terminal fragment and a metalloprotease for the preparation of a pharmaceutical composition for modulating myostatin activation
摘要 <p>The invention provides an in vitro method of decreasing myostatin activation. The method comprises contacting a sample comprising a latent myostatin complex comprising a myostatin pro peptide and a myostatin C-terminal fragment, and a metalloprotease that can cleave the myostatin pro peptide, with an agent that decreases proteolytic cleavage of the pro peptide by the metalloprotease, thereby decreasing myostatin activation. The metalloprotease is a bone morphogenic protein-1/tolloid (BMP-1/TLD) family member and the agent is a peptide selected from the group consisting of SEQ ID NOS: 9-23. Also provided is such an agent for use in decreasing myostatin activation in a subj ect.</p>
申请公布号 IL166651(A) 申请公布日期 2013.12.31
申请号 IL20050166651 申请日期 2005.02.02
申请人 WYETH LLC;WISCONSIN ALUMNI RESEARCH FOUNDATION;THE JOHNS HOPKINS UNIVERSITY 发明人
分类号 A61K;A61K38/00;A61K38/16;A61K38/18;C07K;C07K14/475;C12N;C12N9/64;C12Q 主分类号 A61K
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