MRC Mitochondrial Biology Unit, Cambridge CB2 0XY, UK.
Trends Biochem Sci. 2010 May;35(5):298-307. doi: 10.1016/j.tibs.2009.11.001. Epub 2009 Dec 16.
Mitochondrial uncoupling proteins disengage substrate oxidation from ADP phosphorylation by dissipating the proton electrochemical gradient that is required for ATP synthesis. In doing this, the archetypal uncoupling protein, UCP1, mediates adaptive thermogenesis. By contrast, its paralogues UCP2 and UCP3 are not thought to mediate whole body thermogenesis in mammals. Instead, they have been implicated in a variety of physiological and pathological processes, including protection from oxidative stress, negative regulation of glucose sensing systems and the adaptation of fatty acid oxidation capacity to starving. Although much work has been devoted to how these proteins are activated, little is known of the mechanisms that reverse this activation.
线粒体解偶联蛋白通过耗散合成 ATP 所需的质子电化学梯度,将底物氧化与 ADP 磷酸化分离。这样,典型的解偶联蛋白 UCP1 介导适应性产热。相比之下,其同工酶 UCP2 和 UCP3 被认为不会介导哺乳动物的全身产热。相反,它们与各种生理和病理过程有关,包括对氧化应激的保护、葡萄糖感应系统的负调控以及脂肪酸氧化能力对饥饿的适应。尽管已经进行了大量工作来研究这些蛋白如何被激活,但对于逆转这种激活的机制却知之甚少。