Cortés-Rojo Christian, Calderón-Cortés Elizabeth, Clemente-Guerrero Mónica, Estrada-Villagómez Mirella, Manzo-Avalos Salvador, Mejía-Zepeda Ricardo, Boldogh Istvan, Saavedra-Molina Alfredo
Instituto de Investigaciones Químico-Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Edificio B-3. CU, Morelia, Mich 58030, México.
J Bioenerg Biomembr. 2009 Feb;41(1):15-28. doi: 10.1007/s10863-009-9200-3. Epub 2009 Feb 18.
Lipoperoxidative damage to the respiratory chain proteins may account for disruption in mitochondrial electron transport chain (ETC) function and could lead to an augment in the production of reactive oxygen species (ROS). To test this hypothesis, we investigated the effects of lipoperoxidation on ETC function and cytochromes spectra of Saccharomyces cerevisiae mitochondria. We compared the effects of Fe(2+) treatment on mitochondria isolated from yeast with native (lipoperoxidation-resistant) and modified (lipoperoxidation-sensitive) fatty acid composition. Augmented sensitivity to oxidative stress was observed in the complex III-complex IV segment of the ETC. Lipoperoxidation did not alter the cytochromes content. Under lipoperoxidative conditions, cytochrome c reduction by succinate was almost totally eliminated by superoxide dismutase and stigmatellin. Our results suggest that lipoperoxidation impairs electron transfer mainly at cytochrome b in complex III, which leads to increased resistance to antimycin A and ROS generation due to an electron leak at the level of the Q(O) site of complex III.
呼吸链蛋白的脂过氧化损伤可能是线粒体电子传递链(ETC)功能紊乱的原因,并且可能导致活性氧(ROS)生成增加。为了验证这一假设,我们研究了脂过氧化对酿酒酵母线粒体ETC功能和细胞色素光谱的影响。我们比较了Fe(2+)处理对从具有天然(抗脂过氧化)和修饰(对脂过氧化敏感)脂肪酸组成的酵母中分离出的线粒体的影响。在ETC的复合体III - 复合体IV区段观察到对氧化应激的敏感性增强。脂过氧化并未改变细胞色素含量。在脂过氧化条件下,超氧化物歧化酶和柱晶白霉素几乎完全消除了琥珀酸对细胞色素c的还原作用。我们的结果表明,脂过氧化主要在复合体III中的细胞色素b处损害电子传递,这导致由于复合体III的Q(O)位点水平的电子泄漏而增加了对抗霉素A的抗性和ROS生成。