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TA205, an anti‐talin monoclonal antibody, inhibits integrin–talin interaction
Author(s) -
Xing Baodong,
Thuppal Shalini,
Jedsadayanmata Arom,
Du Xiaoping,
Lam Stephen C.-T.
Publication year - 2006
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/j.febslet.2006.02.077
Subject(s) - integrin , focal adhesion , ferm domain , chemistry , monoclonal antibody , microbiology and biotechnology , epitope , allosteric regulation , actin , biology , antibody , signal transduction , biochemistry , receptor , membrane protein , immunology , integral membrane protein , membrane
Talin mediates integrin signaling by binding to integrin cytoplasmic tails through its FERM domain which consists of F1, F2 and F3 subdomains. TA205, an anti‐talin monoclonal antibody, disrupts actin stress fibers and focal adhesion when microinjected into fibroblasts. Here, we showed that TA205 caused an allosteric inhibition of integrin α IIb β 3 binding to the talin FERM domain and mapped the TA205 epitope to residues 131–150 in talin F1. Furthermore, binding of a talin rod fragment to talin head was partially inhibited by TA205. These findings suggest that talin F1 may be important in regulation of integrin binding and talin head–rod interaction.
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