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首页> 外文期刊>Biochimica et biophysica acta. Bioenergetics >Mitochondrial proton leaks and uncoupling proteins
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Mitochondrial proton leaks and uncoupling proteins

机译:线粒体质子泄漏和解耦蛋白

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摘要

Non-shivering thermogenesis in brown adipose tissue is mediated by uncoupling protein 1 (UCP1), which provides a carefully regulated proton re-entry pathway across the mitochondrial inner membrane operating in parallel to the ATP synthase and allowing respiration, and hence thermogenesis, to be released from the constraints of respiratory control. In the 40 years since UCP1 was first described, an extensive, and frequently contradictory, literature has accumulated, focused on the acute physiological regulation of the protein by fatty acids, purine nucleotides and possible additional factors. The purpose of this review is to examine, in detail, the experimental evidence underlying these proposed mechanisms. Emphasis will be placed on the methodologies employed and their relation to the physiological constraints under which the protein functions in the intact cell. The nature of the endogenous, UCP1-independent, proton leak will also be discussed. Finally, the troubled history of the putative novel uncoupling proteins, UCP2 and UCP3, will be evaluated.
机译:棕色脂肪组织中的不颤动的热生成通过解耦蛋白1(UCP1)来介导,其在与ATP合酶平行的线粒体内膜上提供仔细调节的质子再进入途径并允许呼吸,因此热生成。从呼吸控制的约束中释放。在第一次描述的40年内,累积了广泛,经常矛盾的文献,重点关注蛋白质的脂肪酸,嘌呤核苷酸和可能的额外因素。本综述的目的是详细检查这些拟议机制的实验证据。重点将放置在所用方法上,以及它们与生理学约束的关系,在这种情况下,蛋白质功能在完整细胞中。还将讨论内源性,UCP1无关,质子泄漏的性质。最后,将评估推定的新型解偶联蛋白,UCP2和UCP3的困扰历史。

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