Regulated protein turnover: snapshots of the proteasome in action

被引:187
作者
Bhattacharyya, Sucharita [1 ]
Yu, Houqing [1 ,2 ]
Mim, Carsten [1 ]
Matouschek, Andreas [1 ,2 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
[2] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
26S PROTEASOME; 20S PROTEASOME; STRUCTURAL BASIS; UBIQUITIN RECEPTORS; MOLECULAR ARCHITECTURE; FUNCTIONAL ASYMMETRIES; CUBITUS-INTERRUPTUS; CRYSTAL-STRUCTURE; ATPASE COMPLEX; PORE LOOPS;
D O I
10.1038/nrm3741
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ubiquitin proteasome system (UPS) is the main ATP-dependent protein degradation pathway in the cytosol and nucleus of eukaryotic cells. At its centre is the 26S proteasome, which degrades regulatory proteins and misfolded or damaged proteins. In a major breakthrough, several groups have determined high-resolution structures of the entire 26S proteasome particle in different nucleotide conditions and with and without substrate using cryo-electron microscopy combined with other techniques. These structures provide some surprising insights into the functional mechanism of the proteasome and will give invaluable guidance for genetic and biochemical studies of this key regulatory system.
引用
收藏
页码:122 / 133
页数:12
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