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内体运输中的Rab GTP酶和驱动蛋白马达

Rab GTPases and kinesin motors in endosomal trafficking.

作者信息

Delevoye Cédric, Goud Bruno

机构信息

Institut Curie, PSL Research University, Paris, France; CNRS UMR 144, Structure and Membrane Compartments, Paris, France.

Institut Curie, PSL Research University, Paris, France; CNRS UMR 144, Molecular Mechanisms of Intracellular Transport, Paris, France.

出版信息

Methods Cell Biol. 2015;130:235-46. doi: 10.1016/bs.mcb.2015.05.004. Epub 2015 Jul 7.

Abstract

The endocytic pathway is composed of distinct types of endosomes that vary in shape, function, and molecular composition. In addition, endosomes are highly dynamic structures that continuously receive, sort, and deliver molecules to other organelles. Among organizing machineries that contribute to endosomal functions, Rab GTPases and kinesin motors play critical roles. Rab proteins define the identity of endosomal subdomains by recruiting set of effectors among which kinesins shape and transport membranous carriers along the microtubule network. In this review, we provide detailed protocols from live cell imaging to electron microscopy and biochemical approaches to address how Rab and kinesin proteins cooperate molecularly and functionally within the endocytic pathway.

摘要

内吞途径由不同类型的内体组成,这些内体在形状、功能和分子组成上各不相同。此外,内体是高度动态的结构,不断接收、分选并将分子递送至其他细胞器。在有助于内体功能的组织机制中,Rab GTP酶和驱动蛋白发挥着关键作用。Rab蛋白通过招募一组效应器来定义内体亚结构域的特性,其中驱动蛋白沿着微管网络塑造并运输膜性载体。在本综述中,我们提供了从活细胞成像到电子显微镜以及生化方法的详细方案,以探讨Rab和驱动蛋白如何在内吞途径中进行分子和功能协作。

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