Promiscuity of GABAA‐receptor β3 subunits as demonstrated by their presence in α1, α2 and α3 subunit‐containing receptor subpopulations

Abstract
Polyclonal antibodies were raised in rabbits against the GABAA-receptor β3 subunit peptide sequence, KQSMPREGHGRHMDR-NH2 coupled to keyhole limpet haemocyanin. These anti-β3 379–393 antibodies immunoprecipitated in a dose-dependent manner specific benzodiazepine agonist binding sites from Na+ deoxycholate extracts of bovine cerebral cortex. In immunoblots, anti-β3 379–393 antibodies recognised two species with Mfr 59 900 and Mfr 57 200 in all preparations tested, which included crude detergent-solubilised, benzodiazepine affinity chromatography-purified receptor, anti-α1 324–341 antibody, anti-Cys α2 414–424 antibody and anti-Cys α3 454–467 antibody immunoaffinity-purified GABAA-receptor subpopulations. These results provide evidence for the ubiquity and promiscuity of the GABAA-receptor β3 subunit