Mammalian xanthine oxidoreductase - mechanism of transition from xanthine dehydrogenase to xanthine oxidase

被引:279
|
作者
Nishino, Tomoko [1 ]
Okamoto, Ken [1 ]
Eger, Bryan T. [2 ,3 ,4 ,5 ]
Pai, Emil F. [2 ,3 ,4 ,5 ]
Nishino, Takeshi [1 ]
机构
[1] Nippon Med Sch, Dept Biochem & Mol Biol, Bunkyo Ku, Tokyo 1138602, Japan
[2] Univ Toronto, Dept Biochem, Toronto, ON, Canada
[3] Univ Toronto, Dept Med Phys, Toronto, ON, Canada
[4] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[5] Univ Hlth Network, Div Canc Genom & Proteom, Ontario Canc Inst, Toronto, ON, Canada
关键词
cation interaction; flavin semiquinone; hydrogen peroxide; iron-sulfur center; molybdopterin cofactor; reactive oxygen species; superoxide; xanthine dehydrogenase; xanthine oxidase; xanthine oxidoreductase;
D O I
10.1111/j.1742-4658.2008.06489.x
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
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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页码:3278 / 3289
页数:12
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