Faculty, Staff and Student Publications
Publication Date
5-1-2025
Journal
Nature
DOI
10.1038/s41586-025-08770-0
PMID
40140570
PMCID
PMC12074995
PubMedCentral® Posted Date
3-26-2025
PubMedCentral® Full Text Version
Post-print
Abstract
Ionotropic glutamate receptors (iGluRs) are tetrameric ligand-gated ion channels that mediate most excitatory neurotransmission1. iGluRs are gated by glutamate, where on glutamate binding, they open their ion channels to enable cation influx into postsynaptic neurons, initiating signal transduction1,2. The structural mechanics of how glutamate gating occurs in full-length iGluRs is not well understood. Here, using the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid subtype iGluR (AMPAR), we identify the glutamate-gating mechanism. AMPAR activation by glutamate is augmented at physiological temperatures. By preparing AMPARs for cryogenic-electron microscopy at these temperatures, we captured the glutamate-gating mechanism. Activation by glutamate initiates ion channel opening that involves all ion channel helices hinging away from the pore axis in a motif that is conserved across all iGluRs. Desensitization occurs when the local dimer pairs decouple and enables closure of the ion channel below through restoring the channel hinges and refolding the channel gate. Our findings define how glutamate gates iGluRs, provide foundations for therapeutic design and demonstrate how physiological temperatures can alter iGluR function.
Keywords
Animals, Humans, Cryoelectron Microscopy, Glutamic Acid, Ion Channel Gating, Models, Molecular, Protein Multimerization, Receptors, AMPA, Temperature
Published Open-Access
yes
Recommended Citation
Kumar Mondal, Anish; Carrillo, Elisa; Jayaraman, Vasanthi; et al., "Glutamate Gating of Ampa-Subtype iGluRs at Physiological Temperatures" (2025). Faculty, Staff and Student Publications. 4531.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/4531
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