gamma-Aminobutyric acid/benzodiazepine receptor protein carries binding sites for both ligands on both two major peptide subunits

Biochem Biophys Res Commun. 1988 Jun 30;153(3):1006-11. doi: 10.1016/s0006-291x(88)81328-7.

Abstract

Affinity column-purified GABA-benzodiazepine receptor proteins from human, cow, and rat brain were photoaffinity labeled with both [3H]flunitrazepam and [3H]muscimol and examined by gel electrophoresis in sodium dodecyl sulfate. Using high receptor protein concentrations (1 microM), the benzodiazepine ligand [3H]flunitrazepam was incorporated covalently primarily into the expected 52 kiloDalton major subunit but also significantly into a second 57 kiloDalton peptide. Likewise the GABA ligand [3H]muscimol photolabeled primarily the 57 kiloDalton peptide but also to some extent the 52 kiloDalton peptide. This cross-labeling suggests strongly that both major subunits carry binding sites for both GABA and benzodiazepine.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Affinity Labels / metabolism
  • Animals
  • Binding Sites
  • Cattle
  • Flunitrazepam / metabolism*
  • Humans
  • Ligands / metabolism
  • Macromolecular Substances
  • Molecular Weight
  • Muscimol / metabolism*
  • Photochemistry
  • Rats
  • Receptors, GABA-A / metabolism*

Substances

  • Affinity Labels
  • Ligands
  • Macromolecular Substances
  • Receptors, GABA-A
  • Muscimol
  • Flunitrazepam