硫氧还蛋白
蛋白酶体
蛋白质亚单位
蛋白质水解
生物化学
细胞内
细胞质
细胞生物学
半胱氨酸
泛素
丝氨酸
化学
生物
酶
基因
作者
Katrine M. Andersen,Louise Madsen,Søren Prag,Anders H. Johnsen,Colin A. Semple,Klavs B. Hendil,Rasmus Hartmann‐Petersen
标识
DOI:10.1074/jbc.m900016200
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.
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