氧化磷酸化
电子传输链
线粒体
细胞器
化学
生物化学
线粒体内膜
电泳
线粒体呼吸链
生物
生物物理学
线粒体DNA
呼吸链
聚丙烯酰胺
凝胶电泳
细胞生物学
聚丙烯酰胺凝胶电泳
分子生物学
基因
酶
作者
Pooja Jha,Xu Wang,Johan Auwerx
标识
DOI:10.1002/9780470942390.mo150182
摘要
Abstract Mitochondria are cellular organelles that harvest energy in the form of ATP through a process termed oxidative phosphorylation (OXPHOS), which occurs via the protein complexes of the electron transport chain (ETC). In recent years it has become unequivocally clear that mitochondrial complexes of the ETC are not static entities in the inner mitochondrial membrane. These complexes are dynamic and in mammals they aggregate in different stoichiometric combinations to form supercomplexes (SCs) or respirasomes. It has been proposed that the net respiration is more efficient via SCs than via isolated complexes. However, it still needs to be determined whether the activity of a particular SC is associated with a disease etiology. Here we describe a simplified method to visualize and assess in‐gel activity of SCs and the individual complexes with good resolution using blue native polyacrylamide gel electrophoresis (BN‐PAGE). © 2016 by John Wiley & Sons, Inc.
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