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Membrane Potential Greatly Enhances Superoxide Generation by the Cytochrome bc1 Complex Reconstituted into Phospholipid Vesicles

机译:膜电位极大地增强了细胞色素bc1复合物重构为磷脂囊泡的超氧化物生成。

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摘要

The mitochondrial cytochrome bc1 complex (ubiquinol/cytochrome c oxidoreductase) is generally thought to generate superoxide anion that participates in cell signaling and contributes to cellular damage in aging and degenerative disease. However, the isolated, detergent-solubilized bc1 complex does not generate measurable amounts of superoxide except when inhibited by antimycin. In addition, indirect measurements of superoxide production by cells and isolated mitochondria have not clearly resolved the contribution of the bc1 complex to the generation of superoxide by mitochondria in vivo, nor did they establish the effect, if any, of membrane potential on superoxide formation by this enzyme complex. In this study we show that the yeast cytochrome bc1 complex does generate significant amounts of superoxide when reconstituted into phospholipid vesicles. The rate of superoxide generation by the reconstituted bc1 complex increased exponentially with increased magnitude of the membrane potential, a finding that is compatible with the suggestion that membrane potential inhibits electron transfer from the cytochrome bL to bH hemes, thereby promoting the formation of a ubisemiquinone radical that interacts with oxygen to generate superoxide. When the membrane potential was further increased, by the addition of nigericin or by the imposition of a diffusion potential, the rate of generation of superoxide was further accelerated and approached the rate obtained with antimycin. These findings suggest that the bc1 complex may contribute significantly to superoxide generation by mitochondria in vivo, and that the rate of superoxide generation can be controlled by modulation of the mitochondrial membrane potential.
机译:通常认为线粒体细胞色素bc1复合物(泛醇/细胞色素c氧化还原酶)会产生超氧阴离子,该阴离子参与细胞信号传导,并在衰老和退行性疾病中导致细胞损伤。但是,分离的去污剂增溶的bc1复合物不会产生可测量量的超氧化物,除非被抗霉素抑制。此外,间接测量细胞和分离的线粒体产生的超氧化物并没有清楚地分辨出bc1复合体对体内线粒体产生超氧化物的贡献,也没有确定膜电位对由膜生成超氧化物的影响。这种酶复合物。在这项研究中,我们表明,酵母细胞色素bc1复合物在重构为磷脂囊泡时确实会产生大量的超氧化物。重组bc1络合物产生的超氧化物的速率随膜电位的增加呈指数增加,这一发现与膜电位抑制电子从细胞色素bL向bH血红素的转移,从而促进泛半醌自由基形成的暗示相符。与氧气相互作用生成超氧化物。当膜电位通过添加尼日利亚霉素或施加扩散电位而进一步增加时,超氧化物的产生速率进一步加速并接近抗霉素获得的速率。这些发现表明,bc1复合物可能在体内通过线粒体显着促进了超氧化物的产生,并且可以通过调节线粒体膜电位来控制超氧化物的产生速率。

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