Glucose 6-phosphate release of wild-type and mutant human brain hexokinases from mitochondria

J Biol Chem. 2005 Nov 18;280(46):38403-9. doi: 10.1074/jbc.M506943200. Epub 2005 Sep 15.

Abstract

One molecule of glucose 6-phosphate inhibits brain hexokinase (HKI) with high affinity by binding to either one of two sites located in distinct halves of the enzyme. In addition to potent inhibition, glucose 6-phosphate releases HKI from the outer leaflet of mitochondria; however, the site of glucose 6-phosphate association responsible for the release of HKI is unclear. The incorporation of a C-terminal polyhistidine tag on HKI facilitates the rapid purification of recombinant enzyme from Escherichia coli. The tagged construct has N-formyl methionine as its first residue and has mitochondrial association properties comparable with native brain hexokinases. Release of wild-type and mutant hexokinases from mitochondria by glucose 6-phosphate follow equilibrium models, which explain the release phenomenon as the repartitioning of ligand-bound HKI between solution and the membrane. Mutations that block the binding of glucose 6-phosphate to the C-terminal half of HKI have little or no effect on the glucose 6-phosphate release. In contrast, mutations that block glucose 6-phosphate binding to the N-terminal half require approximately 7-fold higher concentrations of glucose 6-phosphate for the release of HKI. Results here implicate a primary role for the glucose 6-phosphate binding site at the N-terminal half of HKI in the release mechanism.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Alanine / chemistry
  • Animals
  • Binding Sites
  • Brain / enzymology*
  • Brain / metabolism
  • Circular Dichroism
  • Dose-Response Relationship, Drug
  • Escherichia coli / metabolism
  • Glucose-6-Phosphate / metabolism*
  • Hexokinase / chemistry*
  • Hexokinase / genetics*
  • Hexokinase / physiology*
  • Histidine / chemistry
  • Humans
  • Kinetics
  • Ligands
  • Liver / enzymology
  • Liver / metabolism
  • Magnesium / chemistry
  • Mitochondria / metabolism*
  • Models, Chemical
  • Mutation
  • N-Formylmethionine / chemistry
  • Plasmids / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Swine
  • Threonine / chemistry

Substances

  • Ligands
  • polyhistidine
  • Threonine
  • N-Formylmethionine
  • Histidine
  • Glucose-6-Phosphate
  • Adenosine Triphosphate
  • Hexokinase
  • Magnesium
  • Alanine