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Electron Tunneling Rates in Respiratory Complex?I Are Tuned for Efficient Energy Conversion

机译:调节呼吸复合物中的电子隧穿速率?我进行了有效能量转换的调整

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摘要

Respiratory complex I converts the free energy of ubiquinone reduction by NADH into a proton motive force, a redox reaction catalyzed by flavin mononucleotide(FMN) and a chain of seven iron–sulfur centers. Electron transfer rates between the centers were determined by ultrafast freeze-quenching and analysis by EPR and UV/Vis spectroscopy. The complex rapidly oxidizes three NADH molecules. The electron-tunneling rate between the most distant centers in the middle of the chain depends on the redox state of center N2 at the end of the chain, and is sixfold slower when N2 is reduced. The conformational changes that accompany reduction of N2 decrease the electronic coupling of the longest electron-tunneling step. The chain of iron–sulfur centers is not just a simple electron-conducting wire; it regulates the electron-tunneling rate synchronizing it with conformation-mediated proton pumping, enabling efficient energy conversion. Synchronization of rates is a principle means of enhancing the specificity of enzymatic reactions.
机译:呼吸复合物I将NADH还原泛醌还原的自由能转化为质子原动力,黄素单核苷酸(FMN)催化的氧化还原反应和七个铁硫中心链。中心之间的电子转移速率通过超快冷冻猝灭法确定,并通过EPR和UV / Vis光谱分析。该配合物迅速氧化三个NADH分子。链中间最远的中心之间的电子隧穿速率取决于链末端中心N2的氧化还原状态,而当N2还原时,电子隧穿速率慢六倍。伴随N 2还原的构象变化降低了最长电子隧穿步骤的电子耦合。铁-硫中心链不仅是一条简单的电子导电线,它还具有许多特殊的功能。它调节电子隧穿速率,使其与构象介导的质子泵浦同步,从而实现有效的能量转换。速率同步是增强酶促反应特异性的主要手段。

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