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化学门控电子转移。一种加速和调节生物电子转移速率的方式。

Chemically gated electron transfer. A means of accelerating and regulating rates of biological electron transfer.

作者信息

Davidson Victor L

机构信息

Department of Biochemistry, University of Mississippi Medical Center, Jackson 39216-4505, USA.

出版信息

Biochemistry. 2002 Dec 17;41(50):14633-6. doi: 10.1021/bi026812k.

Abstract

Long-range protein electron transfer [ET] reactions may be relatively slow because of long ET distance and low driving force. It is possible to dramatically increase the rate of such nonadiabatic reactions by using an adiabatic chemical reaction to activate the system for rapid ET. Three such examples are discussed; nitrogenase, pyruvate:ferredoxin oxidoreductase, and the methylamine dehydrogenase-amicyanin complex. In each example, the faster activated ET reaction is gated (i.e., rate-limited) by the chemical reaction. However, the reaction rate is still orders of magnitude greater than that of the ungated true ET reaction in the absence of chemical activation. Models are presented to describe the mechanisms of activation in the context of ET theory, and the relevance of such chemically gated ET to the regulation of metabolism is discussed.

摘要

由于电子转移(ET)距离长且驱动力低,长程蛋白质电子转移反应可能相对较慢。通过利用绝热化学反应激活系统以实现快速电子转移,可以显著提高此类非绝热反应的速率。本文讨论了三个这样的例子:固氮酶、丙酮酸:铁氧化还原蛋白氧化还原酶以及甲胺脱氢酶 - 蓝铜蛋白复合物。在每个例子中,更快的激活电子转移反应受化学反应控制(即限速)。然而,反应速率仍比无化学激活时的非控制真实电子转移反应速率高几个数量级。本文提出了模型来描述电子转移理论背景下的激活机制,并讨论了这种化学控制电子转移与代谢调节的相关性。

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