Bénit Paule, Goncalves Sergio, Philippe Dassa Emmanuel, Brière Jean-Jacques, Martin Gail, Rustin Pierre
Inserm, U676, Paris, F-75019 France and Université Paris 7, Faculté de médecine Denis Diderot, IFR02, Paris, France.
Clin Chim Acta. 2006 Dec;374(1-2):81-6. doi: 10.1016/j.cca.2006.05.034. Epub 2006 Jun 2.
BACKGROUND: The measurement of the activities of the five complexes comprising the respiratory chain has proven to be a major challenge when a limiting amount of biological material is available. Here we report a set of three convenient assays that allows this measurement under such circumstances. METHODS: One assay relies on the sequential addition of reagents to measure first complex IV activity, followed by complex II+III, and then glycerol-3-phosphate dehydrogenase+complex III activities and finally isolated complex III activity. A second assay measures the activity of complex II followed by glycerol-3-phosphate dehydrogenase and isocitrate dehydrogenase. A third assay measures rotenone-sensitive complex I activity and subsequently oligomycin-sensitive complex V activity. RESULTS: These assays have been successfully used on extracts of small numbers of human cells displaying various defects in the respiratory chain, and on frozen tissue homogenates of retina and very early mouse embryos. CONCLUSIONS: The strength of this set of assays lies both in its rapid and simple execution and its capacity for immediate detection of partial defects, because each activity can be compared with one or two other activities measured in the same sample.
背景:当生物材料的量有限时,对构成呼吸链的五个复合体的活性进行测量已被证明是一项重大挑战。在此,我们报告了一组三种便捷的检测方法,可在这种情况下进行此类测量。 方法:一种检测方法依赖于依次添加试剂,首先测量复合体IV的活性,接着是复合体II + III的活性,然后是甘油-3-磷酸脱氢酶 + 复合体III的活性,最后是分离的复合体III的活性。第二种检测方法测量复合体II的活性,接着是甘油-3-磷酸脱氢酶和异柠檬酸脱氢酶的活性。第三种检测方法测量对鱼藤酮敏感的复合体I的活性,随后是对寡霉素敏感的复合体V的活性。 结果:这些检测方法已成功应用于显示呼吸链各种缺陷的少量人类细胞提取物,以及视网膜和极早期小鼠胚胎的冷冻组织匀浆。 结论:这组检测方法的优势在于其执行快速简便,且能够立即检测到部分缺陷,因为每种活性都可以与在同一样品中测量的一或两种其他活性进行比较。
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