Feedback Regulation and Time Hierarchy of Oxidative Phosphorylation in Cardiac Mitochondria

Biophys J. 2016 Feb 23;110(4):972-80. doi: 10.1016/j.bpj.2016.01.003.

Abstract

To determine how oxidative ATP synthesis is regulated in the heart, the responses of cardiac mitochondria oxidizing pyruvate to alterations in [ATP], [ADP], and inorganic phosphate ([Pi]) were characterized over a range of steady-state levels of extramitochondrial [ATP], [ADP], and [Pi]. Evolution of the steady states of the measured variables with the flux of respiration shows that: (1) a higher phosphorylation potential is achieved by mitochondria at higher [Pi] for a given flux of respiration; (2) the time hierarchy of oxidative phosphorylation is given by phosphorylation subsystem, electron transport chain, and substrate dehydrogenation subsystems listed in increasing order of their response times; (3) the matrix ATP hydrolysis mass action ratio [ADP] × [Pi]/[ATP] provides feedback to the substrate dehydrogenation flux over the entire range of respiratory flux examined in this study; and finally, (4) contrary to previous models of regulation of oxidative phosphorylation, [Pi] does not modulate the activity of complex III.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Cell Respiration
  • Feedback, Physiological*
  • Kinetics
  • Mitochondria, Heart / metabolism*
  • Oxidative Phosphorylation*
  • Phosphates / metabolism
  • Proton-Translocating ATPases / metabolism
  • Rats
  • Rats, Wistar
  • Succinate-CoA Ligases / metabolism
  • Temperature

Substances

  • Phosphates
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Proton-Translocating ATPases
  • Succinate-CoA Ligases