Regulatory proteins of F1F0-ATPase: role of ATPase inhibitor

J Bioenerg Biomembr. 1990 Feb;22(1):27-38. doi: 10.1007/BF00762843.

Abstract

An intrinsic ATPase inhibitor inhibits the ATP-hydrolyzing activity of mitochondrial F1F0-ATPase and is released from its binding site on the enzyme upon energization of mitochondrial membranes to allow phosphorylation of ADP. The mitochondrial activity to synthesize ATP is not influenced by the absence of the inhibitor protein. The enzyme activity to hydrolyze ATP is induced by dissipation of the membrane potential in the absence of the inhibitor. Thus, the inhibitor is not responsible for oxidative phosphorylation, but acts only to inhibit ATP hydrolysis by F1F0-ATPase upon deenergization of mitochondrial membranes. The inhibitor protein forms a regulatory complex with two stabilizing factors, 9K and 15K proteins, which facilitate the binding of the inhibitor to F1F0-ATPase and stabilize the resultant inactivated enzyme. The 9K protein, having a sequence very similar to the inhibitor, binds directly to F1 in a manner similar to the inhibitor. The 15K protein binds to the F0 part and holds the inhibitor and the 9K protein on F1F0-ATPase even when one of them is detached from the F1 part.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • ATPase Inhibitory Protein
  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / metabolism
  • Amino Acid Sequence
  • Escherichia coli / enzymology
  • Mitochondria / enzymology*
  • Molecular Sequence Data
  • Phosphorylation
  • Proteins / metabolism*
  • Proton-Translocating ATPases / antagonists & inhibitors*
  • Proton-Translocating ATPases / metabolism
  • Sequence Homology, Nucleic Acid
  • Yeasts / enzymology

Substances

  • Proteins
  • Adenosine Diphosphate
  • Adenosine Triphosphate
  • Proton-Translocating ATPases