[3H]muscimol photolabels the gamma-aminobutyric acid receptor binding site on a peptide subunit distinct from that labeled with benzodiazepines

Biochem Biophys Res Commun. 1986 Aug 14;138(3):1308-14. doi: 10.1016/s0006-291x(86)80425-9.

Abstract

Affinity column-purified GABA-benzodiazepine receptor protein from bovine brain was photoaffinity labeled with both [3H]flunitrazepam and [3H]muscimol. Gel electrophoresis in sodium dodecyl sulfate revealed that the benzodiazepine binding site labeled with [3H]flunitrazepam was primarily associated with a major peptide subunit revealed by protein staining with Mr = 52 kiloDaltons, with minor labeling of a second peptide of Mr = 57 kiloDaltons, corresponding to a second major stained band. Covalent incorporation of [3H]muscimol was limited to the 57 kiloDalton band, with no labeling of the 52 kiloDalton peptide, showing that the GABA binding site is carried by a subunit distinct from that carrying the benzodiazepine binding site.

Publication types

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

MeSH terms

  • Affinity Labels
  • Animals
  • Benzodiazepines / metabolism*
  • Binding Sites
  • Cattle
  • Cerebral Cortex
  • Flunitrazepam / metabolism
  • In Vitro Techniques
  • Muscimol / metabolism*
  • Photochemistry
  • Receptors, GABA-A / metabolism*
  • Time Factors
  • Ultraviolet Rays

Substances

  • Affinity Labels
  • Receptors, GABA-A
  • Benzodiazepines
  • Muscimol
  • Flunitrazepam