The ESCRT complexes: Structure and mechanism of a membrane-trafficking network

被引:439
作者
Hurley, James H. [1 ]
Emr, Scott D.
机构
[1] US Dept HHS, NIDDKD, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
来源
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE | 2006年 / 35卷
关键词
ubiquitin; sorting; endocytosis; lysosomes;
D O I
10.1146/annurev.biophys.35.040405.102126
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ESCRT complexes and associated proteins comprise a major pathway for the lysosomal degradation of transmembrane proteins and are critical for receptor downregulation, budding of the HIV virus, and other normal and pathological cell processes. The ESCRT system is conserved from yeast to humans. The ESCRT complexes form a network that recruits monoubiquitinated proteins and drives their internalization into lumenal vesicles within a type of endosome known as a multivesicular body. The structures and interactions of many of the components have been determined over the past three years, revealing mechanisms for membrane and cargo recruitment and for complex assembly.
引用
收藏
页码:277 / 298
页数:22
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