Literature DB >> 2471518

Valinomycin binds stoichiometrically to cytochrome c oxidase and changes its structure and function.

D Steverding1, B Kadenbach.   

Abstract

Valinomycin binds to soluble and reconstituted cytochrome c oxidase (COX) in a stoichiometric manner, as shown by a spectral shift of the oxidized gamma-band. No spectral change is found with nigericin or 18-crown-6 and in the absence of potassium ions. Titration of the proton pumping activity of reconstituted COX with valinomycin reached a maximum of H+/e- - 0.73 after addition of 1 mole of valinomycin per mole of reconstituted COX. It is concluded that K+-translocation in proton-pumping COX vesicles occurs via enzyme-bound valinomycin.

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Year:  1989        PMID: 2471518     DOI: 10.1016/s0006-291x(89)80121-4

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

Review 1.  Evolutionary aspects of cytochrome c oxidase.

Authors:  B Kadenbach; A Stroh; F J Hüther; A Reimann; D Steverding
Journal:  J Bioenerg Biomembr       Date:  1991-04       Impact factor: 2.945

2.  The K(+)-ionophores nonactin and valinomycin interact differently with the protein of reconstituted cytochrome c oxidase.

Authors:  D Steverding; B Kadenbach
Journal:  J Bioenerg Biomembr       Date:  1990-04       Impact factor: 2.945

3.  Protons, pumps, and potentials: control of cytochrome oxidase.

Authors:  P Nicholls; P Butko
Journal:  J Bioenerg Biomembr       Date:  1993-04       Impact factor: 2.945

4.  Phospholipid vesicles containing bovine heart mitochondrial cytochrome c oxidase exhibit proton translocating activity in the presence of gramicidin.

Authors:  L J Prochaska; K S Wilson
Journal:  Arch Biochem Biophys       Date:  1991-10       Impact factor: 4.013

  4 in total

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