Widespread and enzyme-independent Nε-acetylation and Nε-succinylation of proteins in the chemical conditions of the mitochondrial matrix

J Biol Chem. 2013 Oct 4;288(40):29036-45. doi: 10.1074/jbc.M113.486753. Epub 2013 Aug 13.

Abstract

Alterations in mitochondrial protein acetylation are implicated in the pathophysiology of diabetes, the metabolic syndrome, mitochondrial disorders, and cancer. However, a viable mechanism responsible for the widespread acetylation in mitochondria remains unknown. Here, we demonstrate that the physiologic pH and acyl-CoA concentrations of the mitochondrial matrix are sufficient to cause dose- and time-dependent, but enzyme-independent acetylation and succinylation of mitochondrial and nonmitochondrial proteins in vitro. These data suggest that protein acylation in mitochondria may be a chemical event facilitated by the alkaline pH and high concentrations of reactive acyl-CoAs present in the mitochondrial matrix. Although these results do not exclude the possibility of enzyme-mediated protein acylation in mitochondria, they demonstrate that such a mechanism may not be required in its unique chemical environment. These findings may have implications for the evolutionary roles that the mitochondria-localized SIRT3 deacetylase and SIRT5 desuccinylase have in the maintenance of metabolic health.

Keywords: Acetyl Coenzyme A; Acetylation; Metabolic Diseases; Metabolic Regulation; Mitochondrial Metabolism; Nonenzymatic; Sirtuins; Succinyl Coenzyme A; Succinylation; pH Regulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Amino Acid Sequence
  • Animals
  • Catalysis
  • Coenzyme A / metabolism
  • Computational Biology
  • Hydrogen-Ion Concentration
  • Hydroxides / metabolism
  • Kinetics
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / metabolism*
  • Mitochondrial Proteins / chemistry
  • Mitochondrial Proteins / metabolism*
  • Molecular Sequence Data
  • Sirtuin 3 / metabolism
  • Succinates / metabolism*

Substances

  • Hydroxides
  • Mitochondrial Proteins
  • Succinates
  • hydroxide ion
  • Sirtuin 3
  • Coenzyme A