School of Biosciences, University of Kent, Canterbury, UK
Mechanobiology Institute, National University of Singapore, Singapore.
J Cell Biol. 2018 Nov 5;217(11):3776-3784. doi: 10.1083/jcb.201808061. Epub 2018 Sep 25.
Cell adhesion to the extracellular matrix (ECM), mediated by transmembrane receptors of the integrin family, is exquisitely sensitive to biochemical, structural, and mechanical features of the ECM. Talin is a cytoplasmic protein consisting of a globular head domain and a series of α-helical bundles that form its long rod domain. Talin binds to the cytoplasmic domain of integrin β-subunits, activates integrins, couples them to the actin cytoskeleton, and regulates integrin signaling. Recent evidence suggests switch-like behavior of the helix bundles that make up the talin rod domains, where individual domains open at different tension levels, exerting positive or negative effects on different protein interactions. These results lead us to propose that talin functions as a mechanosensitive signaling hub that integrates multiple extracellular and intracellular inputs to define a major axis of adhesion signaling.
细胞通过整联蛋白家族的跨膜受体黏附于细胞外基质(ECM),这种黏附对 ECM 的生化、结构和力学特征极为敏感。塔林是一种细胞质蛋白,由球状头部结构域和一系列形成其长杆状结构域的α-螺旋束组成。塔林与整合素β亚基的细胞质结构域结合,激活整合素,将其与肌动蛋白细胞骨架偶联,并调节整合素信号。最近的证据表明,组成塔林杆状结构域的螺旋束具有类似开关的行为,其中单个结构域在不同的张力水平下打开,对不同的蛋白质相互作用产生正向或负向影响。这些结果使我们提出,塔林作为一种机械敏感信号枢纽发挥作用,整合多种细胞外和细胞内的输入,以确定黏附信号的主要轴。