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

Author:

Brand Martin D.1,Pakay Julian L.1,Ocloo Augustine1,Kokoszka Jason2,Wallace Douglas C.2,Brookes Paul S.3,Cornwall Emma J.1

Affiliation:

1. Medical Research Council Dunn Human Nutrition Unit, Hills Road, Cambridge CB2 2XY, U.K.

2. Center for Mitochondrial Medicine, School of Public Health, Emory University, Atlanta, GA 30322, U.S.A.

3. Department of Molecular and Cellular Pathology, University of Birmingham, Birmingham, AL 35294, U.S.A.

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.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

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