Homomeric GluA2(R) AMPA receptors can conduct when desensitized
Ian D. Coombs,
David Soto,
Thomas P. McGee,
Matthew G. Gold,
Mark Farrant () and
Stuart G. Cull-Candy ()
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Ian D. Coombs: University College London
David Soto: University College London
Thomas P. McGee: University College London
Matthew G. Gold: University College London
Mark Farrant: University College London
Stuart G. Cull-Candy: University College London
Nature Communications, 2019, vol. 10, issue 1, 1-13
Abstract:
Abstract Desensitization is a canonical property of ligand-gated ion channels, causing progressive current decline in the continued presence of agonist. AMPA-type glutamate receptors (AMPARs), which mediate fast excitatory signaling throughout the brain, exhibit profound desensitization. Recent cryo-EM studies of AMPAR assemblies show their ion channels to be closed in the desensitized state. Here we present evidence that homomeric Q/R-edited AMPARs still allow ions to flow when the receptors are desensitized. GluA2(R) expressed alone, or with auxiliary subunits (γ-2, γ-8 or GSG1L), generates large fractional steady-state currents and anomalous current-variance relationships. Our results from fluctuation analysis, single-channel recording, and kinetic modeling, suggest that the steady-state current is mediated predominantly by conducting desensitized receptors. When combined with crystallography this unique functional readout of a hitherto silent state enabled us to examine cross-linked cysteine mutants to probe the conformation of the desensitized ligand binding domain of functioning AMPAR complexes.
Date: 2019
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12280-9
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DOI: 10.1038/s41467-019-12280-9
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