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鱼藤酮和泛醌与线粒体NADH脱氢酶的反应位点。

The reaction sites of rotenone and ubiquinone with mitochondrial NADH dehydrogenase.

作者信息

Singer T P, Ramsay R R

机构信息

Department of Biochemistry and Biophysics, University of California, San Francisco.

出版信息

Biochim Biophys Acta. 1994 Aug 30;1187(2):198-202. doi: 10.1016/0005-2728(94)90110-4.

Abstract

This article summarizes recent studies in the authors' and other laboratories of selective inhibitors acting at the 'rotenone' site and at the Q binding site in the NADH-Q oxidoreductase segment of the respiratory chain. A wide array of inhibitors act at the rotenone site to block electron flux from the enzyme to the Q pool. Using evidence from studies with rotenone, piericidin A, and analogs of the neurotoxic N-methyl-4-phenylpyridinium, we have proposed two binding sites for these inhibitors, both of which must be occupied for complete inhibition of NADH oxidation.

摘要

本文总结了作者实验室及其他实验室近期关于作用于呼吸链NADH-Q氧化还原酶段中“鱼藤酮”位点和Q结合位点的选择性抑制剂的研究。大量抑制剂作用于鱼藤酮位点,以阻断电子从该酶向Q池的流动。利用对鱼藤酮、杀粉蝶菌素A以及神经毒性N-甲基-4-苯基吡啶鎓类似物的研究证据,我们提出了这些抑制剂的两个结合位点,两个位点均被占据才能完全抑制NADH氧化。

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