黄嘌呤脱氢酶
黄嘌呤氧化酶
超氧化物
氧化还原酶
化学
生物化学
活性氧
酶
过氧化氢
黄嘌呤
脱氢酶
作者
Tomoko Nishino,Ken Okamoto,B.T. Eger,E.F. Pai,Takeshi Nishino
出处
期刊:FEBS Journal
[Wiley]
日期:2008-05-30
卷期号:275 (13): 3278-3289
被引量:370
标识
DOI:10.1111/j.1742-4658.2008.06489.x
摘要
Reactive oxygen species are generated by various biological systems, including NADPH oxidases, xanthine oxidoreductase, and mitochondrial respiratory enzymes, and contribute to many physiological and pathological phenomena. Mammalian xanthine dehydrogenase (XDH) can be converted to xanthine oxidase (XO), which produces both superoxide anion and hydrogen peroxide. Recent X‐ray crystallographic and site‐directed mutagenesis studies have revealed a highly sophisticated mechanism of conversion from XDH to XO, suggesting that the conversion is not a simple artefact, but rather has a function in mammalian organisms. Furthermore, this transition seems to involve a thermodynamic equilibrium between XDH and XO; disulfide bond formation or proteolysis can then lock the enzyme in the XO form. In this review, we focus on recent advances in our understanding of the mechanism of conversion from XDH to XO.
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