Structural determinants of integrin recognition by Talin

被引:386
作者
García-Alvarez, B
de Pereda, JM
Calderwood, DA
Ulmer, TS
Critchley, D
Campbell, ID
Ginsberg, MH
Liddington, RC
机构
[1] Burnham Inst, Program Cell Adhes, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 90237 USA
[3] Univ Oxford, Dept Biochem, Oxford OX1 3QU, England
[4] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
关键词
D O I
10.1016/S1097-2765(02)00823-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The binding of cytoplasmic proteins, such as talin, to the cytoplasmic domains of integrin adhesion receptors mediates bidirectional signal transduction. Here we report the crystal structure of the principal integrin binding and activating fragment of talin, alone and in complex with fragments of the beta3 integrin tail. The FERM (four point one, ezrin, radixin, and moesin) domain of talin engages integrins via a novel variant of the canonical phosphotyrosine binding (PTB) domain-NPxY ligand interaction that may be a prototype for FERM domain recognition of transmembrane receptors. In combination with NMR and mutational analysis, our studies reveal the critical interacting elements of both talin and the integrin beta3 tail, providing structural paradigms for integrin linkage to the cell interior.
引用
收藏
页码:49 / 58
页数:10
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