Control of transmembrane charge transfer in cytochrome c oxidase by the membrane potential

被引:22
作者
Bjorck, Markus L. [1 ]
Brzezinski, Peter [1 ]
机构
[1] Stockholm Univ, Dept Biochem & Biophys, Arrhenius Labs Nat Sci, SE-10691 Stockholm, Sweden
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
瑞典研究理事会;
关键词
CATALYZING OXIDATIVE-PHOSPHORYLATION; ACTIVE-SITE TYROSINE; PROTON-TRANSFER; SUBMITOCHONDRIAL PARTICLES; ELECTRON-TRANSFER; PARTIAL RESOLUTION; OXYGEN REDUCTION; MECHANISM; PUMP; TRANSLOCATION;
D O I
10.1038/s41467-018-05615-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The respiratory chain in mitochondria is composed of membrane-bound proteins that couple electron transfer to proton translocation across the inner membrane. These charge-transfer reactions are regulated by the proton electrochemical gradient that is generated and maintained by the transmembrane charge transfer. Here, we investigate this feedback mechanism in cytochrome c oxidase in intact inner mitochondrial membranes upon generation of an electrochemical potential by hydrolysis of ATP. The data indicate that a reaction step that involves proton uptake to the catalytic site and presumably proton translocation is impaired by the potential, but electron transfer is not affected. These results define the order of electron and proton-transfer reactions and suggest that the proton pump is regulated by the transmembrane electrochemical gradient through control of internal proton transfer rather than by control of electron transfer.
引用
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页数:8
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