Weak-acid uncouplers of oxidative phosphorylation. Mechanism of action on thin lipid membranes

Alan Finkelstein

Research output: Contribution to journalArticle

93 Citations (Scopus)

Abstract

Weak-acid uncouplers of oxidative phosphorylation such as p-trifluoromethoxycarbonylcyanidephenylhydrazone, tetrachloro-2-trifluoromethylbenzimidazole, m-chlorocarbonylcyanidephenylhydrazone, and 2,4-dinitrophenol can increase the conductance of thin lipid membranes by several orders of magnitude. In this high conductance state these membranes appear to be ideally selectively permeable to H+ or OH-. We suggest, however, that the primary charge carrier in the membrane is neither H+ or OH-, but rather a dimer formed between the undissociated and dissociated form of the weak acid, and we show that all of the data on the action of these weak acids on thin lipid membranes are consistent with this picture.

Original languageEnglish (US)
Pages (from-to)1-6
Number of pages6
JournalBBA - Bioenergetics
Volume205
Issue number1
DOIs
StatePublished - Apr 7 1970

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Oxidative Phosphorylation
Membrane Lipids
Acids
Membranes
2,4-Dinitrophenol
Charge carriers
Dimers
hydroxide ion

ASJC Scopus subject areas

  • Biophysics
  • Medicine(all)

Cite this

Weak-acid uncouplers of oxidative phosphorylation. Mechanism of action on thin lipid membranes. / Finkelstein, Alan.

In: BBA - Bioenergetics, Vol. 205, No. 1, 07.04.1970, p. 1-6.

Research output: Contribution to journalArticle

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