MRC Laboratory of Molecular Biology, Cambridge CB2 0QH, UK. Electronic address: https://twitter.com/DKampjut.
Institute of Science and Technology Austria, Am Campus 1, 3400 Klosterneuburg, Austria.
Curr Opin Struct Biol. 2022 Jun;74:102350. doi: 10.1016/j.sbi.2022.102350. Epub 2022 Mar 19.
Complex I is one of the major respiratory complexes, conserved from bacteria to mammals. It oxidises NADH, reduces quinone and pumps protons across the membrane, thus playing a central role in the oxidative energy metabolism. In this review we discuss our current state of understanding the structure of complex I from various species of mammals, plants, fungi, and bacteria, as well as of several complex I-related proteins. By comparing the structural evidence from these systems in different redox states and data from mutagenesis and molecular simulations, we formulate the mechanisms of electron transfer and proton pumping and explain how they are conformationally and electrostatically coupled. Finally, we discuss the structural basis of the deactivation phenomenon in mammalian complex I.
复合体 I 是一种主要的呼吸酶复合体,从细菌到哺乳动物都有保守。它氧化 NADH,还原醌并将质子泵过膜,因此在氧化能量代谢中起着核心作用。在这篇综述中,我们讨论了我们目前对来自各种哺乳动物、植物、真菌和细菌的复合体 I 以及几种与复合体 I 相关的蛋白质的结构的理解。通过比较这些系统在不同氧化还原状态下的结构证据以及突变和分子模拟的数据,我们提出了电子转移和质子泵的机制,并解释了它们是如何在构象和静电上偶联的。最后,我们讨论了哺乳动物复合体 I 失活现象的结构基础。