
Cardiolipin stabilized supercomplexes of Saccharomyces cerevisiae respiratory chain complexes III and IV (ubiquinol:cytochrome c oxidoreductase and cytochrome c oxidase, respectively), but was not essential for their formation in the inner mitochondrial membrane because they were found also in a cardiolipin-deficient strain. Reconstitution with cardiolipin largely restored wild-type stability. The putative interface of complexes III and IV comprises transmembrane helices of cytochromes b and c1 and tightly bound cardiolipin. Subunits Rip1p, Qcr6p, Qcr9p, Qcr10p, Cox8p, Cox12p, and Cox13p and cytochrome c were not essential for the assembly of supercomplexes; and in the absence of Qcr6p, the formation of supercomplexes was even promoted. An additional marked effect of cardiolipin concerns cytochrome c oxidase. We show that a cardiolipin-deficient strain harbored almost inactive resting cytochrome c oxidase in the membrane. Transition to the fully active pulsed state occurred on a minute time scale.
Models, Molecular, 570, Binding Sites, Dose-Response Relationship, Drug, Cardiolipins, Protein Conformation, Blotting, Western, Cell Membrane, Cytochromes c1, Digitonin, Cytochromes b, Catalysis, Mitochondria, ATP Synthetase Complexes, Electron Transport Complex IV, Kinetics, Mutation, Electrophoresis, Polyacrylamide Gel, Indicators and Reagents, ddc:570, Dimerization, Phospholipids
Models, Molecular, 570, Binding Sites, Dose-Response Relationship, Drug, Cardiolipins, Protein Conformation, Blotting, Western, Cell Membrane, Cytochromes c1, Digitonin, Cytochromes b, Catalysis, Mitochondria, ATP Synthetase Complexes, Electron Transport Complex IV, Kinetics, Mutation, Electrophoresis, Polyacrylamide Gel, Indicators and Reagents, ddc:570, Dimerization, Phospholipids
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