Pyruvate kinase hyperactivity genetically determined metabolic consequences and molecular characterization

Blood. 1980 Nov;56(5):902-9.

Abstract

Four people from the same family with red cell pyruvate kinase (PK) hyperactivity are described. These people displayed low 2,3-diphosphoglycerate (2,3-DPG) and high adenosine triphosphate (ATP) levels. In vitro metabolism studies of their red cells showed the relationship between the PK activity, low 2,3-DPG, and high ATP levels. The PK electrophoretic pattern of these subjects was abnormal by the presence of several additional bands; one of them migrated like PKM2. PKR from these people was thermounstable and M2-like PK was identical to PKM2 for immunologic reactivity and KO, 5s for phosphoenolpyruvate.

MeSH terms

  • Adenosine Triphosphate / blood
  • Chemical Phenomena
  • Chemistry
  • Diphosphoglyceric Acids / biosynthesis
  • Diphosphoglyceric Acids / blood
  • Electrophoresis, Cellulose Acetate
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Humans
  • Hybridization, Genetic
  • Male
  • Polycythemia / blood
  • Pyruvate Kinase / genetics*
  • Pyruvate Kinase / isolation & purification
  • Pyruvate Kinase / metabolism

Substances

  • Diphosphoglyceric Acids
  • Adenosine Triphosphate
  • Pyruvate Kinase