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A point mutation in the γ(2) subunit of γ-aminobutyric acid type A receptors results in altered benzodiazepine binding site specificity

Benzodiazepines allosterically modulate γ-aminobutyric acid (GABA) evoked chloride currents of γ-aminobutyric acid type A (GABA(A)) receptors. Coexpression of either rat γ(2) or γ(3), in combination with α(1) and β(2) subunits, results both in receptors displaying high [(3)H]Ro 15-1788 affinity. How...

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Bibliografische gegevens
Gepubliceerd in:Proc Natl Acad Sci U S A
Hoofdauteurs: Buhr, Andreas, Sigel, Erwin
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: National Academy of Sciences 1997
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Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC23149/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9238062/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.16.8824
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