ClpXP, an ATP-powered unfolding and protein-degradation machine

被引:357
作者
Baker, Tania A. [1 ,2 ]
Sauer, Robert T. [1 ]
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2012年 / 1823卷 / 01期
关键词
Targeted degradation; Energy-dependent proteolysis; Protein unfolding; Protein translocation; ZINC-BINDING DOMAIN; AAA PLUS PROTEASE; SPECIFICITY-ENHANCING FACTOR; ESCHERICHIA-COLI CLPP; SSRA-TAGGED PROTEINS; DEPENDENT PROTEASES; STRUCTURAL BASIS; MU-TRANSPOSASE; SSPB ADAPTER; MOLECULAR CHAPERONE;
D O I
10.1016/j.bbamcr.2011.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
ClpXP is a AAA+ protease that uses the energy of ATP binding and hydrolysis to perform mechanical work during targeted protein degradation within cells. ClpXP consists of hexamers of a AAA+ ATPase (ClpX) and a tetradecameric peptidase (ClpP). Asymmetric ClpX hexamers bind unstructured peptide tags in protein substrates, unfold stable tertiary structure in the substrate, and then translocate the unfolded polypeptide chain into an internal proteolytic compartment in ClpP. Here, we review our present understanding of ClpXP structure and function, as revealed by two decades of biochemical and biophysical studies. This article is part of a Special Issue entitled: AAA ATPases: Structure and function. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:15 / 28
页数:14
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