THE ESCRT COMPLEXES: Structure and Mechanism of a Membrane-Trafficking Network

Author:

Hurley James H.1,Emr Scott D.2

Affiliation:

1. Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, U.S. Department of Health and Human Services, Bethesda, Maryland 20892-0580;

2. Department of Cellular and Molecular Medicine and Howard Hughes Medical Institute, University of California at San Diego, La Jolla, California 92093-0668;

Abstract

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.

Publisher

Annual Reviews

Subject

Structural Biology,Biophysics

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