Assignment of the CO-sensitive carboxyl group in mitochondrial forms of cytochrome c oxidase using yeast mutants

被引:5
|
作者
Marechal, Amandine [1 ]
Meunier, Brigitte [2 ]
Rich, Peter R. [1 ]
机构
[1] UCL, Glynn Lab Bioenerget, Inst Struct & Mol Biol, London WC1E 6BT, England
[2] CNRS, Ctr Genet Mol, UPR 3404, F-91198 Gif Sur Yvette, France
来源
基金
英国生物技术与生命科学研究理事会;
关键词
Mitochondria; Cytochrome c oxidase; FTIR; Site-directed mutagenesis; Yeast; TRANSFORM INFRARED-SPECTROSCOPY; HEME-COPPER OXIDASES; PARACOCCUS-DENITRIFICANS; RHODOBACTER-SPHAEROIDES; STRUCTURAL-CHANGES; FTIR SPECTROSCOPY; ESCHERICHIA-COLI; SUBUNIT-I; BOVINE; MECHANISM;
D O I
10.1016/j.bbabio.2012.03.036
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
Point mutations of E243D and I67N were introduced into subunit Iota 6histidine-tagged (6H-WT) form of yeast Saccharomyces cerevisiae mitochondrial cytochrome c oxidase. The two mutants (6H-E243D(I) and 6H-I67N(I)) were purified and showed approximate to 50 and 10% of the 6H-WT turnover number. Light-induced CO photolysis FTIR difference spectra of the 6H-WT showed a peak/trough at 1749/1740 cm(-1), as seen in bovine CcO, which downshifted by 7 cm(-1) in D2O. The bands shifted to 1736/1762 cm(-1) in 6H-E243D(I), establishing that the carboxyl group affected by CO binding in mitochondrial CcOs is E243. In 6H-I67N(I), the trough at 1740 cm(-1) was shifted to 1743 cm(-1) and its accompanying peak intensity was greatly reduced. This confirms that the I67N mutation interferes with conformational alterations around E243. This article is part of a Special Issue entitled: 17th European Bioenergetics Conference (EBEC 2012). (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1921 / 1924
页数:4
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