发明名称 Protease Activated Receptor-1 (PAR1) Derived Cytoprotective Polypeptides and Related Methods
摘要 The present invention provides novel PAR lderived cytoprotective oligopeptides or polypeptides which typically contain at least the first 4 N-terminal residues that are substantially identical to the corresponding N-terminal residues of Met1-Arg46 deleted human PAR 1 sequence. These cytoprotective oligopeptides or polypeptides are capable of activating PAR 1 and promoting PAR 1 cytoprotective signaling activities. The invention also provides engineered cells or transgenic non-human animals which harbor in their genome an altered PAR 1 gene that is resistant to cleavage at Arg41 and/or Arg46 residues. Additionally provided in the invention are methods of screening candidate compounds to identity additional cytoprotective compounds or cytoprotective proteases. The invention further provides therapeutic use or methods of employing a PAR 1 derived cytoprotective oligopeptide or polypeptide to treat conditions associated with tissue injuries or undesired apoptosis.
申请公布号 US2015045283(A1) 申请公布日期 2015.02.12
申请号 US201214356692 申请日期 2012.11.07
申请人 THE SCRIPPS RESERCH INSTITUTE 发明人 Mosnier Laurent O.;Griffin John H.
分类号 C07K14/705;A61K38/17 主分类号 C07K14/705
代理机构 代理人
主权项 1. An isolated polypeptide derived from protease activated receptor-1 (PAR1), having at least the first 4 N-terminal residues that are substantially identical to the corresponding N-terminal residues of Met1-Arg46 deleted human PAR1 sequence (SEQ ID NO:2).
地址 La Jolla CA US