Mechanical activation of vinculin binding to talin locks talin in an unfolded conformation

机械激活黏着斑蛋白与踝蛋白的结合,将踝蛋白锁定在未折叠构象中

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作者:Mingxi Yao, Benjamin T Goult, Hu Chen, Peiwen Cong, Michael P Sheetz, Jie Yan

Abstract

The force-dependent interaction between talin and vinculin plays a crucial role in the initiation and growth of focal adhesions. Here we use magnetic tweezers to characterise the mechano-sensitive compact N-terminal region of the talin rod, and show that the three helical bundles R1-R3 in this region unfold in three distinct steps consistent with the domains unfolding independently. Mechanical stretching of talin R1-R3 enhances its binding to vinculin and vinculin binding inhibits talin refolding after force is released. Mutations that stabilize R3 identify it as the initial mechano-sensing domain in talin, unfolding at ∼5 pN, suggesting that 5 pN is the force threshold for vinculin binding and adhesion progression.

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