Bouaouina Mohamed, Harburger David S, Calderwood David A
Department of Pharmacology and Interdepartmental Program in Vascular Biology and Transplantation, Yale University School of Medicine, New Haven, CT, USA.
Methods Mol Biol. 2012;757:325-47. doi: 10.1007/978-1-61779-166-6_20.
Integrin adhesion receptors are essential for the development and functioning of multicellular animals. Integrins mediate cell adhesion to the extracellular matrix and to counter-receptors on adjacent cells, and the ability of integrins to bind extracellular ligands is regulated in response to intracellular signals that act on the short cytoplasmic tails of integrin subunits. Integrin activation, the rapid conversion of integrin receptors from low to high affinity, requires binding of talin to integrin β tails and, once bound, talin provides a connection from activated integrins to the actin cytoskeleton. A wide range of experimental approaches have contributed to the current understanding of the importance of talin in integrin signaling. Here, we describe two methods that have been central to our investigations of talin; a biochemical assay that has allowed characterization of interactions between integrin cytoplasmic tails and talin, and a fluorescent-activated cell-sorting procedure to assess integrin activation in cultured cells expressing talin domains, mutants, dominant negative constructs, or shRNA.
整合素黏附受体对于多细胞动物的发育和功能至关重要。整合素介导细胞与细胞外基质以及相邻细胞上的反受体之间的黏附,并且整合素结合细胞外配体的能力会根据作用于整合素亚基短细胞质尾部的细胞内信号而受到调节。整合素激活,即整合素受体从低亲和力到高亲和力的快速转变,需要踝蛋白与整合素β尾部结合,一旦结合,踝蛋白就会提供从激活的整合素到肌动蛋白细胞骨架的连接。广泛的实验方法有助于当前对踝蛋白在整合素信号传导中重要性的理解。在这里,我们描述了两种对我们研究踝蛋白至关重要的方法;一种生化分析方法,可用于表征整合素细胞质尾部与踝蛋白之间的相互作用,以及一种荧光激活细胞分选程序,用于评估表达踝蛋白结构域、突变体、显性负构建体或短发夹RNA的培养细胞中的整合素激活情况。