Arp2/3复合体和形成蛋白对肌动蛋白丝组装的调控。

Thomas D Pollard
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引用次数: 997

摘要

本文综述了目前已知的肌动蛋白丝在细胞内组装的生化和生物物理机制。这些纤维的组装和拆卸促成了许多类型的细胞运动。许多蛋白质调节肌动蛋白的组装,但Arp2/3复合物和形成蛋白是本综述的重点,因为对它们的了解比其他蛋白质刺激新丝的形成更多。Arp2/3复合体活跃于运动细胞的前缘,在那里它在现有的细丝两侧产生分支。这些细丝的生长产生了突出膜的力量。晶体结构、电子显微照片重建和生物物理实验已经开始描绘出被称为促核因子的蛋白质刺激分支形成的步骤。在细胞分裂和各种类型的肌动蛋白丝束中,成形蛋白成核并支持未分枝的肌动蛋白丝的伸长。Formins与花丝快速生长的末端紧密相连,保护花丝不被封盖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of actin filament assembly by Arp2/3 complex and formins.

This review summarizes what is known about the biochemical and biophysical mechanisms that initiate the assembly of actin filaments in cells. Assembly and disassembly of these filaments contribute to many types of cellular movements. Numerous proteins regulate actin assembly, but Arp2/3 complex and formins are the focus of this review because more is known about them than other proteins that stimulate the formation of new filaments. Arp2/3 complex is active at the leading edge of motile cells, where it produces branches on the sides of existing filaments. Growth of these filaments produces force to protrude the membrane. Crystal structures, reconstructions from electron micrographs, and biophysical experiments have started to map out the steps through which proteins called nucleation-promoting factors stimulate the formation of branches. Formins nucleate and support the elongation of unbranched actin filaments for cytokinesis and various types of actin filament bundles. Formins associate processively with the fast-growing ends of filaments and protect them from capping.

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