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内体分选转运复合体III(ESCRT-III)和Vps4:用于膜出芽和切割的动态多功能工具。

ESCRT-III and Vps4: a dynamic multipurpose tool for membrane budding and scission.

作者信息

Alonso Y Adell Manuel, Migliano Simona M, Teis David

机构信息

Division of Cell Biology, Biocenter, Medical University of Innsbruck, Austria.

出版信息

FEBS J. 2016 Sep;283(18):3288-302. doi: 10.1111/febs.13688. Epub 2016 Mar 8.

Abstract

Complex molecular machineries bud, scission and repair cellular membranes. Components of the multi-subunit endosomal sorting complex required for transport (ESCRT) machinery are enlisted when multivesicular bodies are generated, extracellular vesicles are formed, the plasma membrane needs to be repaired, enveloped viruses bud out of host cells, defective nuclear pores have to be cleared, the nuclear envelope must be resealed after mitosis and for final midbody abscission during cytokinesis. While some ESCRT components are only required for specific processes, the assembly of ESCRT-III polymers on target membranes and the action of the AAA-ATPase Vps4 are mandatory for every process. In this review, we summarize the current knowledge of structural and functional features of ESCRT-III/Vps4 assemblies in the growing pantheon of ESCRT-dependent pathways. We describe specific recruitment processes for ESCRT-III to different membranes, which could be useful to selectively inhibit ESCRT function during specific processes, while not affecting other ESCRT-dependent processes. Finally, we speculate how ESCRT-III and Vps4 might function together and highlight how the characterization of their precise spatiotemporal organization will improve our understanding of ESCRT-mediated membrane budding and scission in vivo.

摘要

复杂的分子机制参与细胞膜的出芽、切割和修复过程。当多泡体形成、细胞外囊泡产生、质膜需要修复、包膜病毒从宿主细胞中出芽、有缺陷的核孔必须清除、有丝分裂后核膜必须重新封闭以及胞质分裂期间进行最终的中体切割时,会招募运输所需的多亚基内体分选复合物(ESCRT)机制的组件。虽然一些ESCRT组件仅在特定过程中需要,但ESCRT-III聚合物在靶膜上的组装以及AAA-ATP酶Vps4的作用对每个过程都是必不可少的。在本综述中,我们总结了在不断增加的依赖ESCRT的途径中,ESCRT-III/Vps4组装体的结构和功能特征的当前知识。我们描述了ESCRT-III到不同膜的特定招募过程,这可能有助于在特定过程中选择性抑制ESCRT功能,同时不影响其他依赖ESCRT的过程。最后,我们推测ESCRT-III和Vps4可能如何协同作用,并强调其精确时空组织的表征将如何提高我们对ESCRT介导的体内膜出芽和切割的理解。

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