ESCRT and Membrane Protein Ubiquitination.

Simona M Migliano, David Teis
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引用次数: 22

Abstract

The ubiquitin-dependent degradation of membrane proteins via the multivesicular body (MVB) pathway requires the Endosomal Sorting Complexes Required for Transport (ESCRT). This molecular machinery is composed of five distinct multi-subunit complexes. On the surface of endosomes, ESCRT-0, -I and -II bind to ubiquitinated membrane proteins, while ESCRT-III and Vps4 bud intraluminal vesicles (ILVs) into the lumen of the endosomes. By working together, ESCRTs package membrane proteins into ILVs and thereby generate MVBs. The fusion of mature MVBs with lysosomes delivers ILVs into the lysosomal lumen where the membrane proteins are degraded. Besides generating ILVs, the ESCRT machinery mediates for topologically related membrane budding processes at the plasma membrane and the nuclear envelop. In this chapter, we briefly discuss membrane protein ubiquitination, endocytosis, and summarize current knowledge on the ESCRT machinery in the MVB pathway.

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ESCRT与膜蛋白泛素化。
膜蛋白通过多泡体(MVB)途径的泛素依赖性降解需要运输所需的内体分选复合物(ESCRT)。这种分子机制由五种不同的多亚基复合物组成。在核内体表面,ESCRT-0、-I和-II与泛素化膜蛋白结合,而ESCRT-III和Vps4在核内体的管腔内形成腔内囊泡(ILVs)。通过协同工作,escrt将膜蛋白包装成ilv,从而产生MVBs。成熟的MVBs与溶酶体的融合将ilv输送到溶酶体腔中,在那里膜蛋白被降解。除了产生ilv外,ESCRT机制还介导质膜和核包膜上拓扑相关的膜出芽过程。在本章中,我们简要地讨论了膜蛋白泛素化、内吞作用,并总结了目前关于MVB通路中ESCRT机制的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
7
期刊介绍: Molecular biology has been providing an overwhelming amount of data on the structural components and molecular machineries of the cell and its organelles and the complexity of intra- and intercellular communication. The molecular basis of hereditary and acquired diseases is beginning to be unravelled, and profound new insights into development and evolutionary biology have been gained from molecular approaches. Progress in Molecular and Subcellular Biology summarises the most recent developments in this fascinating area of biology.
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