Essential active-site lysine of brain glutamate dehydrogenase isoproteins

J Neurochem. 1997 Jul;69(1):418-22. doi: 10.1046/j.1471-4159.1997.69010418.x.

Abstract

Two soluble forms of bovine brain glutamate dehydrogenase (GDH) isoproteins were inactivated by pyridoxal 5'-phosphate. Spectral evidence is presented to indicate that the inactivation proceeds through Schiff's base formation with amino groups of the enzyme. Sodium borohydride reduction of the pyridoxal 5'-phosphate-inactivated GDH isoproteins produced a stable pyridoxyl enzyme derivative that could not be reactivated by dialysis. The pyridoxyl enzyme was studied through fluorescence spectroscopy. No substrates or coenzymes separately gave complete protection against pyridoxal 5'-phosphate. A combination of 10 mM 2-oxoglutarate with 2 mM NADH, however, gave complete protection against the inactivation. Tryptic peptides of the isoproteins, modified with and without protection, resulted in a selective modification of one lysine. In both GDH isoproteins, the sequences of the peptide containing the phosphopyridoxyllysine were clearly identical to sequences of other GDH species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites / physiology
  • Brain / enzymology*
  • Brain Chemistry / physiology
  • Cattle
  • Chromatography, High Pressure Liquid
  • Enzyme Activation / drug effects
  • Glutamate Dehydrogenase / chemistry*
  • Glutamate Dehydrogenase / genetics
  • Glutamate Dehydrogenase / metabolism
  • Humans
  • Isoenzymes / chemistry*
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Ketoglutaric Acids / pharmacology
  • Lysine / chemistry*
  • Lysine / metabolism
  • NAD / pharmacology
  • Peptides / analysis
  • Protein Processing, Post-Translational / physiology
  • Pyridoxal Phosphate / analysis

Substances

  • Isoenzymes
  • Ketoglutaric Acids
  • Peptides
  • NAD
  • Pyridoxal Phosphate
  • Glutamate Dehydrogenase
  • Lysine