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bioRxiv · 10.1101/2023.02.16.528867

Regulated assembly and neurosteroid modulation constrain GABAA receptor pharmacology in vivo

Sun, C.·Zhu, H.·Clark, S. A.·Gouaux, E.
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Abstract

Type A GABA receptors (GABAARs) are the principal inhibitory receptors in the brain and the target of a wide range of clinical agents, including anesthetics, sedatives, hypnotics, and antidepressants. However, our understanding of GABAAR pharmacology has been hindered by the vast number of pentameric assemblies that can be derived from a total 19 different subunits and the lack of structural knowledge of clinically relevant receptors. Here, we isolate native murine GABAAR assemblies containing the widely expressed 1 subunit, and elucidate their structures in complex with drugs used to treat insomnia (zolpidem and flurazepam) and postpartum depression (the neurosteroid allopregnanolone). Using cryo-EM analysis and single-molecule photobleaching experiments, we uncover only three structural populations in the brain: the canonical 1{beta}2{gamma}2 receptor containing two 1 subunits and two unanticipated assemblies containing one 1 and either an 2, 3 or 5 subunit. Both of the noncanonical assemblies feature a more compact arrangement between the transmembrane and extracellular domains. Interestingly, allopregnanolone is bound at the transmembrane /{beta} subunit interface, even when not added to the sample, revealing an important role for endogenous neurosteroids in modulating native GABAARs. Together with structurally engaged lipids, neurosteroids produce global conformational changes throughout the receptor that modify both the pore diameter and binding environments for GABA and insomnia medications. Together, our data reveal that GABAAR assembly is a strictly regulated process that yields a small number of structurally distinct complexes, defining a structural landscape from which subtype-specific drugs can be developed.

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Sun, C., Zhu, H., Clark, S. A., Gouaux, E.. 2023-02-16. Regulated assembly and neurosteroid modulation constrain GABAA receptor pharmacology in vivo. https://doi.org/10.1101/2023.02.16.528867

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