Thioredoxin Txnl1/TRP32 Is a Redox-active Cofactor of the 26 S Proteasome

被引:69
作者
Andersen, Katrine M.
Madsen, Louise
Prag, Soren [2 ]
Johnsen, Anders H. [3 ]
Semple, Colin A. [4 ]
Hendil, Klavs B.
Hartmann-Petersen, Rasmus [1 ]
机构
[1] Univ Copenhagen, Dept Biol, DK-2100 Copenhagen, Denmark
[2] Univ Lisbon, Fac Med, Inst Mol Med, P-1649028 Lisbon, Portugal
[3] Copenhagen Univ Hosp, Dept Clin Biochem, DK-2100 Copenhagen, Denmark
[4] MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
CAENORHABDITIS-ELEGANS; MOLECULAR-CLONING; PROTEIN; IDENTIFICATION; PURIFICATION; DEGRADATION; EXPRESSION; SITE; RECOGNITION; PROTEOMICS;
D O I
10.1074/jbc.M900016200
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 26 S proteasome is a large proteolytic machine, which degrades most intracellular proteins. We found that thioredoxin, Txnl1/TRP32, binds to Rpn11, a subunit of the regulatory complex of the human 26 S proteasome. Txnl1 is abundant, metabolically stable, and widely expressed and is present in the cytoplasm and nucleus. Txnl1 has thioredoxin activity with a redox potential of about -250 mV. Mutant Txnl1 with one active site cysteine replaced by serine formed disulfide bonds to eEF1A1, a substrate-recruiting factor of the 26 S proteasome. eEF1A1 is therefore a likely physiological substrate. In response to knockdown of Txnl1, ubiquitin-protein conjugates were moderately stabilized. Hence, Txnl1 is the first example of a direct connection between protein reduction and proteolysis, two major intracellular protein quality control mechanisms.
引用
收藏
页码:15246 / 15254
页数:9
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