Membrane budding and scission by the ESCRT machinery: it's all in the neck

被引:563
作者
Hurley, James H. [1 ]
Hanson, Phyllis I. [2 ]
机构
[1] NIDDK, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
MULTIVESICULAR BODY PATHWAY; ENDOSOME-ASSOCIATED COMPLEX; AAA ATPASE VPS4; STRUCTURAL BASIS; UBIQUITIN RECOGNITION; SORTING COMPLEX; TRAFFICKING COMPLEX; EAP45-GLUE DOMAIN; VESICLE FORMATION; III RECOGNITION;
D O I
10.1038/nrm2937
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endosomal sorting complexes required for transport (ESCRTs) catalyse one of the most unusual membrane remodelling events in cell biology. ESCRT-I and ESCRT-II direct membrane budding away from the cytosol by stabilizing bud necks without coating the buds and without being consumed in the buds. ESCRT-III cleaves the bud necks from their cytosolic faces. ESCRT-III-mediated membrane neck cleavage is crucial for many processes, including the biogenesis of multivesicular bodies, viral budding, cytokinesis and, probably, autophagy. Recent studies of ultrastructures induced by ESCRT-III overexpression in cells and the in vitro reconstitution of the budding and scission reactions have led to breakthroughs in understanding these remarkable membrane reactions.
引用
收藏
页码:556 / 566
页数:11
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