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本文引用的文献

1
Determination of serum proteins by means of the biuret reaction.通过双缩脲反应测定血清蛋白。
J Biol Chem. 1949 Feb;177(2):751-66.
2
The reactions catalysed by the mitochondrial uncoupling proteins UCP2 and UCP3.由线粒体解偶联蛋白UCP2和UCP3催化的反应。
Biochim Biophys Acta. 2005 Aug 15;1709(1):35-44. doi: 10.1016/j.bbabio.2005.06.002.
3
Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins.线粒体超氧化物:生成、生物学效应及解偶联蛋白的激活
Free Radic Biol Med. 2004 Sep 15;37(6):755-67. doi: 10.1016/j.freeradbiomed.2004.05.034.
4
Superoxide and hydrogen peroxide production by Drosophila mitochondria.果蝇线粒体产生超氧化物和过氧化氢。
Free Radic Biol Med. 2003 Oct 15;35(8):938-48. doi: 10.1016/s0891-5849(03)00464-7.
5
Mitochondrial coupling in vivo in mouse skeletal muscle.小鼠骨骼肌体内的线粒体偶联
Am J Physiol Cell Physiol. 2004 Feb;286(2):C457-63. doi: 10.1152/ajpcell.00237.2003. Epub 2003 Oct 1.
6
Proton conductance and fatty acyl composition of liver mitochondria correlates with body mass in birds.鸟类肝脏线粒体的质子传导率和脂肪酰组成与体重相关。
Biochem J. 2003 Dec 15;376(Pt 3):741-8. doi: 10.1042/BJ20030984.
7
A signalling role for 4-hydroxy-2-nonenal in regulation of mitochondrial uncoupling.4-羟基-2-壬烯醛在调节线粒体解偶联中的信号传导作用。
EMBO J. 2003 Aug 15;22(16):4103-10. doi: 10.1093/emboj/cdg412.
8
Does any yeast mitochondrial carrier have a native uncoupling protein function?是否有任何酵母线粒体载体具有天然的解偶联蛋白功能?
J Bioenerg Biomembr. 2002 Jun;34(3):165-76. doi: 10.1023/a:1016027302232.
9
Proton leak in hepatocytes and liver mitochondria from archosaurs (crocodiles) and allometric relationships for ectotherms.恐龙(鳄鱼)肝细胞和肝脏线粒体中的质子泄漏以及变温动物的异速生长关系。
J Comp Physiol B. 2002 Jul;172(5):387-97. doi: 10.1007/s00360-002-0264-1. Epub 2002 May 4.
10
No evidence for a basal, retinoic, or superoxide-induced uncoupling activity of the uncoupling protein 2 present in spleen or lung mitochondria.未发现脾脏或肺线粒体中存在的解偶联蛋白2有基础、视黄酸或超氧化物诱导的解偶联活性的证据。
J Biol Chem. 2002 Jul 19;277(29):26268-75. doi: 10.1074/jbc.M202535200. Epub 2002 May 14.

线粒体的基础质子传导率取决于腺嘌呤核苷酸转位酶的含量。

The basal proton conductance of mitochondria depends on adenine nucleotide translocase content.

作者信息

Brand Martin D, Pakay Julian L, Ocloo Augustine, Kokoszka Jason, Wallace Douglas C, Brookes Paul S, Cornwall Emma J

机构信息

Medical Research Council Dunn Human Nutrition Unit, Hills Road, Cambridge CB2 2XY, UK.

出版信息

Biochem J. 2005 Dec 1;392(Pt 2):353-62. doi: 10.1042/BJ20050890.

DOI:10.1042/BJ20050890
PMID:16076285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1316271/
Abstract

The basal proton conductance of mitochondria causes mild uncoupling and may be an important contributor to metabolic rate. The molecular nature of the proton-conductance pathway is unknown. We show that the proton conductance of muscle mitochondria from mice in which isoform 1 of the adenine nucleotide translocase has been ablated is half that of wild-type controls. Overexpression of the adenine nucleotide translocase encoded by the stress-sensitive B gene in Drosophila mitochondria increases proton conductance, and underexpression decreases it, even when the carrier is fully inhibited using carboxyatractylate. We conclude that half to two-thirds of the basal proton conductance of mitochondria is catalysed by the adenine nucleotide carrier, independently of its ATP/ADP exchange or fatty-acid-dependent proton-leak functions.

摘要

线粒体的基础质子传导会导致轻度解偶联,可能是代谢率的重要影响因素。质子传导途径的分子本质尚不清楚。我们发现,腺嘌呤核苷酸转位酶同工型1被敲除的小鼠肌肉线粒体的质子传导率是野生型对照的一半。在果蝇线粒体中,由应激敏感B基因编码的腺嘌呤核苷酸转位酶过表达会增加质子传导率,而低表达则会降低质子传导率,即使使用羧基苍术苷将载体完全抑制时也是如此。我们得出结论,线粒体基础质子传导率的一半至三分之二由腺嘌呤核苷酸载体催化,这与其ATP/ADP交换或脂肪酸依赖性质子泄漏功能无关。