CNRS UPR3082, Laboratoire d'Enzymologie et de Biochimie Structurales, Bât. 34, Avenue de la Terrasse, 91198 Gif-sur-Yvette Cedex, France.
Bioessays. 2010 Feb;32(2):119-31. doi: 10.1002/bies.200900123.
The Arp2/3 complex is a molecular machine that generates branched actin networks responsible for membrane remodeling during cell migration, endocytosis, and other morphogenetic events. This machine requires activators, which themselves are multiprotein complexes. This review focuses on recent advances concerning the assembly of stable complexes containing the most-studied activators, N-WASP and WAVE proteins, and the level of regulation that is provided by these complexes. N-WASP is the paradigmatic auto-inhibited protein, which is activated by a conformational opening. Even though this regulation has been successfully reconstituted in vitro with isolated N-WASP, the native dimeric complex with a WIP family protein has unique additional properties. WAVE proteins are part of a pentameric complex, whose basal state and activated state when bound to the Rac GTPase were recently clarified. Moreover, this review attempts to put together diverse observations concerning the WAVE complex in the conceptual frame of an in vivo assembly pathway that has gained support from the recent identification of a precursor.
Arp2/3 复合物是一种分子机器,它生成分支肌动蛋白网络,负责细胞迁移、内吞作用和其他形态发生事件期间的膜重塑。该机器需要激活剂,而激活剂本身就是多蛋白复合物。本综述重点介绍了最近在组装稳定的复合物方面的进展,这些复合物包含研究最多的激活剂 N-WASP 和 WAVE 蛋白,以及这些复合物提供的调节水平。N-WASP 是典型的自动抑制蛋白,通过构象开放而被激活。尽管这种调节已经在体外使用分离的 N-WASP 成功地重建,但与 WIP 家族蛋白的天然二聚复合物具有独特的额外性质。WAVE 蛋白是五聚体复合物的一部分,其基本状态和与 Rac GTPase 结合时的激活状态最近得到了阐明。此外,本综述试图将有关 WAVE 复合物的各种观察结果纳入一个体内组装途径的概念框架中,该途径最近从鉴定前体中得到了支持。