乌头酸酶
弗拉塔辛
伴侣(临床)
线粒体
酶
化学
铁结合蛋白
生物化学
铁硫簇
细胞生物学
生物
转铁蛋白
医学
病理
作者
Anne-Laure Bulteau,Heather A. O’Neill,M C Kennedy,Masao Ikeda‐Saito,Grazia Isaya,Luke I. Szweda
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2004-07-08
卷期号:305 (5681): 242-245
被引量:363
标识
DOI:10.1126/science.1098991
摘要
Numerous degenerative disorders are associated with elevated levels of prooxidants and declines in mitochondrial aconitase activity. Deficiency in the mitochondrial iron-binding protein frataxin results in diminished activity of various mitochondrial iron-sulfur proteins including aconitase. We found that aconitase can undergo reversible citrate-dependent modulation in activity in response to pro-oxidants. Frataxin interacted with aconitase in a citrate-dependent fashion, reduced the level of oxidant-induced inactivation, and converted inactive [3Fe-4S]1+ enzyme to the active [4Fe-4S]2+ form of the protein. Thus, frataxin is an iron chaperone protein that protects the aconitase [4Fe-4S]2+ cluster from disassembly and promotes enzyme reactivation.
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