电子传输链
辅酶Q-细胞色素c还原酶
细胞色素c
线粒体呼吸链
线粒体
焊剂(冶金)
化学
酶
生物物理学
链条(单位)
辅因子
生物化学
呼吸链
电子
立体化学
结晶学
物理
生物
量子力学
有机化学
作者
Esther Lapuente-Brun,Raquel Moreno‐Loshuertos,Rebeca Acı́n-Pérez,Ana Latorre,Carmen Colás,Eduardo Balsa,Ester Perales‐Clemente,Pedro M. Quirós,Enrique Calvo,María Hernández,Plácido Navas,Raquel Cruz,Ãngel Carracedo,Carlos López-Otı́n,Acisclo Pérez‐Martos,Patricio Fernández‐Silva,Erika Fernández‐Vizarra,José Antonio Enrı́quez
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-06-28
卷期号:340 (6140): 1567-1570
被引量:716
标识
DOI:10.1126/science.1230381
摘要
The textbook description of mitochondrial respiratory complexes (RCs) views them as free-moving entities linked by the mobile carriers coenzyme Q (CoQ) and cytochrome c (cyt c). This model (known as the fluid model) is challenged by the proposal that all RCs except complex II can associate in supercomplexes (SCs). The proposed SCs are the respirasome (complexes I, III, and IV), complexes I and III, and complexes III and IV. The role of SCs is unclear, and their existence is debated. By genetic modulation of interactions between complexes I and III and III and IV, we show that these associations define dedicated CoQ and cyt c pools and that SC assembly is dynamic and organizes electron flux to optimize the use of available substrates.
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