The specific molecular basis of the interaction between talin and integrin ß<SUB>3</SUB> has been defined. This specific interaction provides a new therapeutic target; agents that can disrupt this specific interaction should be useful therapeutic agents for a number of significant diseases and conditions including inflammation, heart disease, including myocardial infarction, and tumor metastasis. The present invention includes a chimeric peptide that has high affinity for talin, muteins of talin and integrin ß<SUB>3</SUB> as well as screening methods for agents that can disrupt the interaction between talin and integrin ß<SUB>3</SUB>.
申请公布号
WO2008089152(A3)
申请公布日期
2008.11.06
申请号
WO2008US51016
申请日期
2008.01.14
申请人
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA;OXFORD UNIVERSITY;GINSBERG, MARK;PARTRIDGE, ANTHONY;IAIN, CAMPBELL;WEGENER, KATE
发明人
GINSBERG, MARK;PARTRIDGE, ANTHONY;IAIN, CAMPBELL;WEGENER, KATE