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

Martin D. Brand(MRC Human Nutrition Research), Julian L. Pakay(MRC Human Nutrition Research), Augustine Ocloo(MRC Human Nutrition Research), Jason E. Kokoszka(Emory University), Douglas C. Wallace(Emory University), Paul S. Brookes(University of Alabama at Birmingham), Emma J. Cornwall(MRC Human Nutrition Research)
Biochemical Journal
November 22, 2005
Cited by 406Open Access
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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.


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