Toward an Integrated Structural Model of the 26S Proteasome

被引:39
作者
Foerster, Friedrich [1 ]
Lasker, Keren [2 ,3 ,4 ]
Nickell, Stephan [1 ]
Sali, Andrej [2 ,3 ]
Baumeister, Wolfgang [1 ]
机构
[1] Max Planck Inst Biochem, Dept Biol Struct, D-82152 Martinsried, Germany
[2] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Calif Inst Quantitat Biosci QB3, San Francisco, CA 94158 USA
[4] Tel Aviv Univ, Raymond & Beverly Sackler Fac Exact Sci, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
UCH37 DEUBIQUITINATING ENZYME; PROTEIN-INTERACTION MAP; 19 S REGULATOR; CRYSTAL-STRUCTURE; 20S PROTEASOME; MOLECULAR ARCHITECTURE; SUBUNIT INTERACTIONS; MASS-SPECTROMETRY; 2-HYBRID ANALYSIS; ATPASE SUBUNITS;
D O I
10.1074/mcp.R000002-MCP201
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The 26S proteasome is the end point of the ubiquitin-proteasome pathway and degrades ubiquitylated substrates. It is composed of the 20S core particle (CP), where degradation occurs, and the 19S regulatory particle (RP), which ensures substrate specificity of degradation. Whereas the CP is resolved to atomic resolution, the architecture of the RP is largely unknown. We provide a comprehensive analysis of the current structural knowledge on the RP, including structures of the RP subunits, physical protein-protein interactions, and cryoelectron microscopy data. These data allowed us to compute an atomic model for the CP-AAA-ATPase subcomplex. In addition to this atomic model, further subunits can be mapped approximately, which lets us hypothesize on the substrate path during its degradation. Molecular & Cellular Proteomics 9: 1666-1677, 2010.
引用
收藏
页码:1666 / 1677
页数:12
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