Analyzing the electrogenicity of cytochrome c oxidase

被引:8
作者
Kim, Ilsoo [1 ]
Warshel, Arieh [1 ]
机构
[1] Univ Southern Calif, Dept Chem, Los Angeles, CA 90089 USA
基金
瑞典研究理事会; 美国国家科学基金会;
关键词
electrogenicity; membrane potential; proton transfer; electron transfer; PROTON-PUMPING MECHANISM; COARSE-GRAINED MODELS; HEME-COPPER OXIDASES; RHODOBACTER-SPHAEROIDES; MEMBRANE-PROTEINS; PARACOCCUS-DENITRIFICANS; THERMUS-THERMOPHILUS; ELECTRON-TRANSFER; GATING CHARGE; D-CHANNEL;
D O I
10.1073/pnas.1608118113
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
Measurements of voltage changes in response to charge separation within membrane proteins can offer fundamental information on spectroscopically "invisible" steps. For example, results from studies of voltage changes associated with electron and proton transfer in cytochrome c oxidase could, in principle, be used to discriminate between different theoretical models describing the molecular mechanism of proton pumping. Earlier analyses of data from these measurements have been based on macroscopic considerations that may not allow for exploring the actual molecular mechanisms. Here, we have used a coarse-grained model describing the relation between observed voltage changes and specific charge-transfer reactions, which includes an explicit description of the membrane, the electrolytes, and the electrodes. The results from these calculations offer mechanistic insights at the molecular level. Our main conclusion is that previously assumed mechanistic evidence that was based on electrogenic measurements is not unique. However, the ability of our calculations to obtain reliable voltage changes means that we have a tool that can be used to describe a wide range of electrogenic charge transfers in channels and transporters, by combining voltage measurements with other experiments and simulations to analyze new mechanistic proposals.
引用
收藏
页码:7810 / 7815
页数:6
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