Sun Li, Noel Jeffrey K, Levine Herbert, Onuchic José N
Center for Theoretical Biological Physics, Rice University, Houston, Texas.
Center for Theoretical Biological Physics, Rice University, Houston, Texas; Max Delbrück Center, Berlin, Germany.
Biophys J. 2017 Oct 17;113(8):1697-1710. doi: 10.1016/j.bpj.2017.08.037.
Focal adhesions are dynamic constructs at the leading edge of migrating cells, linking them to the extracellular matrix and enabling force sensing and transmission. The lifecycle of a focal adhesion is a highly coordinated process involving spatial and temporal variations of protein composition, interaction, and cellular tension. The assembly of focal adhesions requires the recruitment and activation of vinculin. Vinculin is present in the cytoplasm in an autoinhibited conformation in which its tail is held pincerlike by its head domains, further stabilized by two high-affinity head-tail interfaces. Vinculin has binding sites for talin and F-actin, but effective binding requires vinculin activation to release its head-tail associations. In migrating cells, it has been shown that the locations of vinculin activation coincide with areas of high cellular tension, and that the highest recorded tensions across vinculin are associated with adhesion assembly. Here, we use a structure-based model to investigate vinculin activation by talin modulated by tensile force generated by transient associations with F-actin. We show that vinculin activation may proceed from an intermediate state stabilized by partial talin-vinculin association. There is a low-force regime and a high-force regime where vinculin activation is dominated by two different pathways with distinct responses to force. Specifically, at zero or low forces, vinculin activation requires substantial destabilization of the main head-tail interface, which is rigid and undergoes very limited fluctuations, despite the other being relatively flexible. This pathway is not significantly affected by force; instead, higher forces favor an alternative pathway, which seeks to release the vinculin tail from its pincerlike head domains before destabilizing the head-tail interfaces. This pathway has a force-sensitive activation barrier and is significantly accelerated by force. Experimental data of vinculin during various stages of the focal adhesion lifecycle are consistent with the proposed force-regulated activation pathway.
粘着斑是迁移细胞前沿的动态结构,将细胞与细胞外基质相连,实现力的感知与传递。粘着斑的生命周期是一个高度协调的过程,涉及蛋白质组成、相互作用和细胞张力的时空变化。粘着斑的组装需要纽蛋白的募集和激活。纽蛋白以自抑制构象存在于细胞质中,其尾部被头部结构域钳状夹住,通过两个高亲和力的头尾界面进一步稳定。纽蛋白有与踝蛋白和F-肌动蛋白的结合位点,但有效的结合需要纽蛋白激活以释放其头尾关联。在迁移细胞中,已表明纽蛋白激活的位置与高细胞张力区域重合,并且记录到的跨纽蛋白的最高张力与粘着斑组装相关。在此,我们使用基于结构的模型来研究由与F-肌动蛋白的瞬时关联产生的拉力调节的踝蛋白对纽蛋白的激活作用。我们表明,纽蛋白激活可能从由部分踝蛋白-纽蛋白关联稳定的中间状态开始。存在一个低力状态和一个高力状态,其中纽蛋白激活由两条不同的途径主导,对力有不同的响应。具体而言,在零力或低力时,纽蛋白激活需要主头尾界面的大量去稳定化,该界面是刚性的且波动非常有限,尽管另一个相对灵活。这条途径不受力的显著影响;相反,更高的力有利于另一条途径,即在使头尾界面去稳定化之前,试图将纽蛋白尾部从其钳状头部结构域中释放出来。这条途径有一个力敏感的激活屏障,并被力显著加速。粘着斑生命周期各个阶段的纽蛋白实验数据与所提出的力调节激活途径一致。