Altered allosteric regulation of muscle 6-phosphofructokinase causes Tarui disease

Biochem Biophys Res Commun. 2012 Oct 12;427(1):133-7. doi: 10.1016/j.bbrc.2012.09.024. Epub 2012 Sep 17.

Abstract

Tarui disease is a glycogen storage disease (GSD VII) and characterized by exercise intolerance with muscle weakness and cramping, mild myopathy, myoglobinuria and compensated hemolysis. It is caused by mutations in the muscle 6-phosphofructokinase (Pfk). Pfk is an oligomeric, allosteric enzyme which catalyzes one of the rate-limiting steps of the glycolysis: the phosphorylation of fructose 6-phosphate at position 1. Pfk activity is modulated by a number of regulators including adenine nucleotides. Recent crystal structures from eukaryotic Pfk displayed several allosteric adenine nucleotide binding sites. Functional studies revealed a reciprocal linkage between the activating and inhibitory allosteric binding sites. Herein, we showed that Asp(543)Ala, a naturally occurring disease-causing mutation in the activating binding site, causes an increased efficacy of ATP at the inhibitory allosteric binding site. The reciprocal linkage between the activating and inhibitory binding sites leads to reduced enzyme activity and therefore to the clinical phenotype. Pharmacological blockage of the inhibitory allosteric binding site or highly efficient ligands for the activating allosteric binding site may be of therapeutic relevance for patients with Tarui disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine / chemistry
  • Alanine / genetics
  • Allosteric Regulation
  • Animals
  • Asparagine / chemistry
  • Asparagine / genetics
  • Binding Sites / genetics
  • Glycogen Storage Disease Type VII / enzymology*
  • Glycogen Storage Disease Type VII / genetics
  • Humans
  • Ligands
  • Mice
  • Muscle, Skeletal / enzymology*
  • Mutation
  • Phosphofructokinase-1 / chemistry
  • Phosphofructokinase-1 / genetics
  • Phosphofructokinase-1 / metabolism*
  • Protein Conformation
  • Rabbits

Substances

  • Ligands
  • Asparagine
  • Phosphofructokinase-1
  • Alanine