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人线粒体复合物 I 的组装因子及其在疾病中的缺陷。

Assembly factors of human mitochondrial complex I and their defects in disease.

机构信息

Department of Biochemistry, La Trobe University, Melbourne, VIC, Australia.

出版信息

IUBMB Life. 2010 Jul;62(7):497-502. doi: 10.1002/iub.335.

Abstract

NADH-ubiquinone oxidoreductase (complex I) is a large, multimeric enzyme complex involved in the generation of ATP by oxidative phosphorylation. Complex I is comprised of 45 subunits which must be assembled together in a coordinated process to form the mature holoenzyme. In recent years, much progress has been made into understanding how complex I is assembled and the work provides potential insights into the biogenesis of other multisubunit membrane complexes. For complex I assembly to proceed effectively, a group of proteins termed "assembly factors" are required. A number of these assembly factors have now been identified and characterized; however, their exact roles in complex I biogenesis are not yet fully understood. This review summarizes the current model of human complex I assembly and the roles played by different assembly factors at early, mid, and late assembly stages. Defects in assembly factors which disrupt complex I assembly and contribute to human disease pathogenesis will also be discussed.

摘要

烟酰胺腺嘌呤二核苷酸-泛醌氧化还原酶(复合物 I)是一种大型的、多聚体的酶复合物,参与氧化磷酸化过程中 ATP 的生成。复合物 I 由 45 个亚基组成,这些亚基必须在协调的过程中组装在一起,形成成熟的全酶。近年来,人们在理解复合物 I 如何组装方面取得了很大进展,这项工作为其他多亚基膜复合物的生物发生提供了潜在的见解。为了使复合物 I 有效地组装,需要一组称为“组装因子”的蛋白质。现在已经鉴定和表征了许多这样的组装因子;然而,它们在复合物 I 生物发生中的确切作用尚未完全理解。这篇综述总结了人类复合物 I 组装的当前模型,以及不同组装因子在早期、中期和晚期组装阶段所扮演的角色。还将讨论组装因子的缺陷如何破坏复合物 I 的组装,并导致人类疾病的发病机制。

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