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Vol. 54, Issue 6, 1097-1105, December 1998

The Benzodiazepine Binding Pocket of Recombinant alpha 1beta 2gamma 2 gamma -Aminobutyric AcidA Receptors: Relative Orientation of Ligands and Amino Acid Side Chains

Erwin Sigel, Martin T. Schaerer, Andreas Buhr, and Roland Baur

Department of Pharmacology, University of Bern, CH-3010 Bern, Switzerland.

Wild-type alpha 1beta 2gamma 2 gamma -aminobutyric acid (GABA)A receptors and receptors containing a point-mutated subunit gamma 2F77Y were expressed by transient transfection in human embryonic kidney 293 cells. Mutant receptors bound the benzodiazepine binding site ligand [3H]flumazenil with similar, subnanomolar affinity as wild-type receptor. Displacement studies with diazepam showed that the affinity for this compound was reduced 250-fold on mutation, indicating that the tyrosine hydroxyl group interferes with diazepam binding. This differential behavior then was used to find the chemical entity presumably interacting with the phenyalanine residue in position 77 of the gamma 2 subunit of wild-type receptors. Thirty-four substances were analyzed in this respect. Our results suggest that the phenyl substituent of diazepam is located close to gamma F77. Similarly, we investigated the possible location of alpha 1T206 and gamma 2M130. Electrophysiological data obtained with the wild-type receptor furthermore suggest a simple overlap between positive allosteric modulators acting at the benzodiazepine binding site with its antagonists.

Copyright © 1998 by The American Society for Pharmacology and Experimental Therapeutics


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Copyright © 1998 by the American Society for Pharmacology and Experimental Therapeutics