Pollard Thomas D
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520-8103, USA.
Annu Rev Biophys Biomol Struct. 2007;36:451-77. doi: 10.1146/annurev.biophys.35.040405.101936.
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.
本综述总结了关于细胞中启动肌动蛋白丝组装的生化和生物物理机制的已知信息。这些丝的组装和解聚促成了多种类型的细胞运动。众多蛋白质调节肌动蛋白组装,但Arp2/3复合物和formin是本综述的重点,因为相对于其他刺激新丝形成的蛋白质,我们对它们了解更多。Arp2/3复合物在运动细胞的前沿活跃,在那里它在现有丝的侧面产生分支。这些丝的生长产生力使膜突出。晶体结构、电子显微镜照片的重建以及生物物理实验已开始描绘出成核促进因子刺激分支形成的步骤。formin为胞质分裂和各种类型的肌动蛋白丝束形成核并支持无分支肌动蛋白丝的延伸。formin与丝的快速生长末端持续结合并保护它们不被封端。