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线粒体质子泄漏与解偶联蛋白

Mitochondrial proton leak and the uncoupling proteins.

作者信息

Stuart J A, Brindle K M, Harper J A, Brand M D

机构信息

Department of Biochemistry, University of Cambridge, UK.

出版信息

J Bioenerg Biomembr. 1999 Oct;31(5):517-25. doi: 10.1023/a:1005456725549.

Abstract

An energetically significant leak of protons occurs across the mitochondrial inner membranes of eukaryotic cells. This seemingly wasteful proton leak accounts for at least 20% of the standard metabolic rate of a rat. There is evidence that it makes a similar contribution to standard metabolic rate in a lizard. Proton conductance of the mitochondrial inner membrane can be considered as having two components: a basal component present in all mitochondria, and an augmentative component, which may occur in tissues of mammals and perhaps of some other animals. The uncoupling protein of brown adipose tissue, UCP1, is a clear example of such an augmentative component. The newly discovered UCP1 homologs, UCP2, UCP3, and brain mitochondrial carrier protein 1 (BMCP1) may participate in the augmentative component of proton leak. However, they do not appear to catalyze the basal leak, as this is observed in mitochondria from cells which apparently lack these proteins. Whereas UCP1 plays an important role in thermogenesis, the evidence that UCP2 and UCP3 do likewise remains equivocal.

摘要

在真核细胞的线粒体内膜上,质子发生了大量的泄漏,这在能量方面具有重要意义。这种看似浪费的质子泄漏至少占大鼠标准代谢率的20%。有证据表明,它对蜥蜴的标准代谢率也有类似的贡献。线粒体内膜的质子传导可被认为有两个组成部分:一个是所有线粒体中都存在的基础部分,另一个是增强部分,它可能出现在哺乳动物以及其他一些动物的组织中。棕色脂肪组织的解偶联蛋白UCP1就是这种增强部分的一个明显例子。新发现的UCP1同源物UCP2、UCP3和脑线粒体载体蛋白1(BMCP1)可能参与质子泄漏的增强部分。然而,它们似乎并不催化基础泄漏,因为在明显缺乏这些蛋白质的细胞的线粒体中也观察到了基础泄漏。虽然UCP1在产热中起重要作用,但UCP2和UCP3同样如此的证据仍然不明确。

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