Department of Cardiovascular & Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Protein Sci. 2021 Mar;30(3):531-542. doi: 10.1002/pro.4014. Epub 2020 Dec 30.
Focal adhesions (FAs) are integrin-containing protein complexes regulated by a network of hundreds of protein-protein interactions. They are formed in a spatiotemporal manner upon the activation of integrin transmembrane receptors, which is crucial to trigger cell adhesion and many other cellular processes including cell migration, spreading and proliferation. Despite decades of studies, a detailed molecular level understanding on how FAs are organized and function is lacking due to their highly complex and dynamic nature. However, advances have been made on studying key integrin activators, talin and kindlin, and their associated proteins, which are major components of nascent FAs critical for initiating the assembly of mature FAs. This review will discuss the structural and functional findings of talin and kindlin and their immediate interaction network, which will shed light upon the architecture of nascent FAs and how they act as seeds for FA assembly to dynamically regulate diverse adhesion-dependent physiological and pathological responses.
焦点黏附(FA)是由数百个蛋白-蛋白相互作用网络调控的整联蛋白包含蛋白复合物。它们在整合素跨膜受体激活时以时空方式形成,这对于触发细胞黏附和许多其他细胞过程包括细胞迁移、扩散和增殖至关重要。尽管经过了几十年的研究,但由于其高度复杂和动态的性质,对于 FA 如何组织和发挥功能的详细分子水平的理解仍然缺乏。然而,在研究关键的整合素激活剂 talin 和 kindlin 及其相关蛋白方面已经取得了进展,它们是新生 FA 的主要组成部分,对于启动成熟 FA 的组装至关重要。这篇综述将讨论 talin 和 kindlin 及其直接相互作用网络的结构和功能发现,这将揭示新生 FA 的结构以及它们如何作为 FA 组装的种子,以动态调节多样化的黏附依赖性生理和病理反应。