The allosteric ATP-inhibition of cytochrome c oxidase activity is reversibly switched on by cAMP-dependent phosphorylation

FEBS Lett. 2000 Jan 21;466(1):130-4. doi: 10.1016/s0014-5793(99)01773-1.

Abstract

In previous studies the allosteric inhibition of cytochrome c oxidase at high intramitochondrial ATP/ADP-ratios via binding of the nucleotides to the matrix domain of subunit IV was demonstrated. Here we show that the allosteric ATP-inhibition of the isolated bovine heart enzyme is switched on by cAMP-dependent phosphorylation with protein kinase A of subunits II (and/or III) and Vb, and switched off by subsequent incubation with protein phosphatase 1. It is suggested that after cAMP-dependent phosphorylation of cytochrome c oxidase mitochondrial respiration is controlled by the ATP/ADP-ratio keeping the proton motive force Deltap low, and the efficiency of energy transduction high. After Ca(2+)-induced dephosphorylation this control is lost, accompanied by increase of Deltap, slip of proton pumping (decreased H(+)/e(-) stoichiometry), and increase of the rate of respiration and ATP-synthesis at a decreased efficiency of energy transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / antagonists & inhibitors*
  • Adenosine Triphosphate / metabolism
  • Allosteric Regulation
  • Animals
  • Calcium / pharmacology
  • Cattle
  • Cyclic AMP / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Electron Transport Complex IV / antagonists & inhibitors*
  • Electron Transport Complex IV / metabolism
  • Energy Metabolism
  • In Vitro Techniques
  • Kinetics
  • Mitochondria, Liver / enzymology
  • Myocardium / enzymology
  • Phosphorylation

Substances

  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Cyclic AMP
  • Electron Transport Complex IV
  • Cyclic AMP-Dependent Protein Kinases
  • Calcium