Inactivation and dissociation of S-adenosylmethionine synthetase by modification of sulfhydryl groups and its possible occurrence in cirrhosis

Hepatology. 1990 Feb;11(2):216-22. doi: 10.1002/hep.1840110210.

Abstract

Catalytically active human and rat liver S-adenosylmethionine synthetase exists mainly in tetramer and dimer form. In liver biopsy samples from cirrhotic patients a marked reduction in total S-adenosylmethionine synthetase activity and a specific loss of the tetrameric form of the enzyme exist. We have investigated the possible role of sulfhydryl groups in maintaining the structure and activity of S-adenosylmethionine synthetase. Both forms of S-adenosylmethionine synthetase are rapidly inactivated by N-ethylmaleimide, and the loss of enzyme activity correlates with the incorporation of approximately 2 moles N-ethylmaleimide per mole of subunit. In addition, reaction with N-ethylmaleimide resulted in displacement of the tetramer-dimer equilibrium of the enzyme toward the dimer, but no monomer was detected under these conditions. A catalytically active monomeric S-adenosylmethionine synthetase was detected in the cytosolic extract from a liver biopsy sample from a cirrhotic patient, supporting our model for the structure of S-adenosylmethionine synthetase. Because treatment of S-adenosylmethionine synthetase with N-ethylmaleimide resembles the situation of this enzyme in cirrhotic patients, it is proposed that impaired protection of the enzyme from oxidizing agents caused by a decreased synthesis of glutathione can explain the diminished synthesis of S-adenosylmethionine in liver cirrhosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatography, Gel
  • Ethylmaleimide / pharmacology
  • Glutathione / biosynthesis
  • Humans
  • Liver Cirrhosis / enzymology*
  • Methionine Adenosyltransferase / antagonists & inhibitors
  • Methionine Adenosyltransferase / metabolism*
  • Molecular Weight
  • Oxidation-Reduction
  • Rats
  • Sulfhydryl Compounds
  • Transferases / metabolism*

Substances

  • Sulfhydryl Compounds
  • Transferases
  • Methionine Adenosyltransferase
  • Glutathione
  • Ethylmaleimide