Liu Jia-Jia
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
CAS Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China.
Traffic. 2017 Jun;18(6):336-347. doi: 10.1111/tra.12475. Epub 2017 Mar 28.
Most of the long-range intracellular movements of vesicles, organelles and other cargoes are driven by microtubule (MT)-based molecular motors. Cytoplasmic dynein, a multisubunit protein complex, with the aid of dynactin, drives transport of a wide variety of cargoes towards the minus end of MTs. In this article, I review our current understanding of the mechanisms underlying spatiotemporal regulation of dynein-dynactin-driven vesicular transport with a special emphasis on the many steps of directional movement along MT tracks. These include the recruitment of dynein to MT plus ends, the activation and processivity of dynein, and cargo recognition and release by the motor complex at the target membrane. Furthermore, I summarize the most recent findings about the fine control mechanisms for intracellular transport via the interaction between the dynein-dynactin motor complex and its vesicular cargoes.
大多数囊泡、细胞器和其他货物的长距离细胞内运动是由基于微管(MT)的分子马达驱动的。胞质动力蛋白是一种多亚基蛋白复合体,在动力蛋白激活蛋白的帮助下,驱动各种货物向微管的负端运输。在本文中,我回顾了我们目前对动力蛋白-动力蛋白激活蛋白驱动的囊泡运输时空调节机制的理解,特别强调了沿微管轨道定向运动的多个步骤。这些步骤包括动力蛋白在微管正端的募集、动力蛋白的激活和持续性,以及马达复合体在靶膜处对货物的识别和释放。此外,我总结了关于通过动力蛋白-动力蛋白激活蛋白马达复合体与其囊泡货物之间的相互作用进行细胞内运输的精细控制机制的最新发现。