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

机译:机械结合纽蛋白的激活蛋白将塔林锁定在未折叠的构象中

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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.
机译:塔林蛋白与新蛋白之间的力依赖性相互作用在粘着斑的形成和生长中起着至关重要的作用。在这里,我们使用磁性镊子表征了塔林棒的机械敏感紧凑型N末端区域,并显示了该区域中的三个螺旋束R1-R3以三个不同的步骤展开,这与域独立展开是一致的。 talin R1-R3的机械拉伸增强了其与纽蛋白的结合力,并且纽扣蛋白结合抑制了力释放后talin的折叠。使R3稳定的突变将其识别为塔林的初始机械感测结构域,在〜5?pN时展开,表明5?pN是纽蛋白结合和粘附进程的力阈值。

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