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能量转换型NADH:醌氧化还原酶(复合体I)。

Energy converting NADH:quinone oxidoreductase (complex I).

作者信息

Brandt Ulrich

机构信息

Universität Frankfurt, Fachbereich Medizin, Zentrum der Biologischen Chemie, D-60590 Frankfurt am Main, Germany.

出版信息

Annu Rev Biochem. 2006;75:69-92. doi: 10.1146/annurev.biochem.75.103004.142539.

Abstract

NADH

quinone oxidoreductase (complex I) pumps protons across the inner membrane of mitochondria or the plasma membrane of many bacteria. Human complex I is involved in numerous pathological conditions and degenerative processes. With 14 central and up to 32 accessory subunits, complex I is among the largest membrane-bound protein assemblies. The peripheral arm of the L-shaped molecule contains flavine mononucleotide and eight or nine iron-sulfur clusters as redox prosthetic groups. Seven of the iron-sulfur clusters form a linear electron transfer chain between flavine and quinone. In most organisms, the seven most hydrophobic subunits forming the core of the membrane arm are encoded by the mitochondrial genome. Most central subunits have evolved from subunits of different hydrogenases and bacterial Na+/H+ antiporters. This evolutionary origin is reflected in three functional modules of complex I. The coupling mechanism of complex I most likely involves semiquinone intermediates that drive proton pumping through redox-linked conformational changes.

摘要

NADH

醌氧化还原酶(复合体I)可将质子泵过线粒体的内膜或许多细菌的质膜。人类复合体I参与众多病理状况和退行性过程。复合体I由14个核心亚基和多达32个辅助亚基组成,是最大的膜结合蛋白组装体之一。L形分子的外周臂含有黄素单核苷酸和八个或九个铁硫簇作为氧化还原辅基。其中七个铁硫簇在黄素和醌之间形成线性电子传递链。在大多数生物体中,构成膜臂核心的七个最疏水亚基由线粒体基因组编码。大多数核心亚基由不同氢化酶和细菌Na+/H+反向转运蛋白的亚基进化而来。这种进化起源体现在复合体I的三个功能模块中。复合体I的偶联机制很可能涉及半醌中间体,其通过氧化还原相关的构象变化驱动质子泵出。

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