Epsin而不是AP-2支持内吞网格蛋白包被囊泡的重建。

IF 3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
FEBS Letters Pub Date : 2020-07-01 Epub Date: 2020-05-22 DOI:10.1002/1873-3468.13801
Jan Brod, Andrea Hellwig, Felix T Wieland
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引用次数: 7

摘要

在受体介导的内吞作用中,网格蛋白包被囊泡(ccv)的形成是一个机制完善的过程,其中网格蛋白、接头蛋白复合物AP-2和大GTPase动力蛋白起着至关重要的作用。为了更深入地了解这一过程的机制,我们建立了一个基于巨型单层囊泡(GUV)的体外CCV重构系统,该系统包含化学定义的成分和全长重组蛋白clathrin, AP-2, epin -1和dynamin-2。我们的结果支持主要的模型,其中GTP水解动力蛋白是产生ccv的先决条件。引人注目的是,在接近生理浓度的试剂中,epsin-1本身不具有分裂的倾向,但它是芽形成所必需的,而AP-2和网格蛋白是不够的。因此,我们的研究表明epsin-1是网格蛋白包被芽成熟的重要因素,这是囊泡产生的先决条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epsin but not AP-2 supports reconstitution of endocytic clathrin-coated vesicles.

Formation of clathrin-coated vesicles (CCVs) in receptor-mediated endocytosis is a mechanistically well-established process, in which clathrin, the adaptor protein complex AP-2, and the large GTPase dynamin play crucial roles. In order to obtain more mechanistic insight into this process, here we established a giant unilamellar vesicle (GUV)-based in vitro CCV reconstitution system with chemically defined components and the full-length recombinant proteins clathrin, AP-2, epsin-1, and dynamin-2. Our results support the predominant model in which hydrolysis of GTP by dynamin is a prerequisite to generate CCVs. Strikingly, in this system at near physiological concentrations of reagents, epsin-1 alone does not have the propensity for scission but is required for bud formation, whereas AP-2 and clathrin are not sufficient. Thus, our study reveals that epsin-1 is an important factor for the maturation of clathrin coated buds, a prerequisite for vesicle generation.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
6.60
自引率
2.90%
发文量
303
审稿时长
1 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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