Mitochondrial proton leak and the uncoupling protein 1 homologues

被引:143
作者
Stuart, JA
Cadenas, S
Jekabsons, MB
Roussel, D
Brand, MD
机构
[1] MRC, Dunn Human Nutr Unit, Cambridge CB2 2XY, England
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2001年 / 1504卷 / 01期
关键词
mitochondrion; proton conductance; basal metabolic rate; respiration; UCP1; UCP2; BMCP1; fatty acid; brown adipose tissue; thermogenesis; zebrafish; carp;
D O I
10.1016/S0005-2728(00)00243-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial proton leak is the largest single contributor to the standard metabolic rate (SMR) of a rat, accounting for about 20% of SMR. Yet the mechanisms by which proton leak occurs are incompletely understood. The available evidence suggests that both phospholipids and proteins in the mitochondrial inner membrane are important determinants of proton conductance. The uncoupling protein 1 homologues (e.g. UCP2, UCP3) may play a role in mediating proton leak, but it is unlikely they account for all of the observed proton conductance. Experimental data regarding the functions of these proteins include important ambiguities and contradictions which must be addressed before their function can be confirmed. The physiological role of the proton leak, and of the uncoupling protein 1 homologues, remains similarly unclear. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:144 / 158
页数:15
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