Structure, function, and pharmacology of glutamate receptor ion channels
Many physiologic effects of l-glutamate, the major excitatory neurotransmitter in the
mammalian central nervous system, are mediated via signaling by ionotropic glutamate …
mammalian central nervous system, are mediated via signaling by ionotropic glutamate …
Structural and functional architecture of AMPA-type glutamate receptors and their auxiliary proteins
IH Greger, JF Watson, SG Cull-Candy - Neuron, 2017 - cell.com
AMPA receptors (AMPARs) are tetrameric ion channels that together with other ionotropic
glutamate receptors (iGluRs), the NMDA and kainate receptors, mediate a majority of …
glutamate receptors (iGluRs), the NMDA and kainate receptors, mediate a majority of …
Human TRPV1 structure and inhibition by the analgesic SB-366791
Pain therapy has remained conceptually stagnant since the opioid crisis, which highlighted
the dangers of treating pain with opioids. An alternative addiction-free strategy to …
the dangers of treating pain with opioids. An alternative addiction-free strategy to …
Allosteric modulation as a unifying mechanism for receptor function and regulation
JP Changeux, A Christopoulos - Cell, 2016 - cell.com
Four major receptor families enable cells to respond to chemical and physical signals from
their proximal environment. The ligand-and voltage-gated ion channels, G-protein-coupled …
their proximal environment. The ligand-and voltage-gated ion channels, G-protein-coupled …
Channel opening and gating mechanism in AMPA-subtype glutamate receptors
Abstract AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid)-subtype ionotropic
glutamate receptors mediate fast excitatory neurotransmission throughout the central …
glutamate receptors mediate fast excitatory neurotransmission throughout the central …
[HTML][HTML] Opening of glutamate receptor channel to subconductance levels
MV Yelshanskaya, DS Patel, CM Kottke, MG Kurnikova… - Nature, 2022 - nature.com
Ionotropic glutamate receptors (iGluRs) are tetrameric ligand-gated ion channels that open
their pores in response to binding of the agonist glutamate,–. An ionic current through a …
their pores in response to binding of the agonist glutamate,–. An ionic current through a …
Modulation of GluA2–γ5 synaptic complex desensitization, polyamine block and antiepileptic perampanel inhibition by auxiliary subunit cornichon-2
SP Gangwar, LY Yen, MV Yelshanskaya… - Nature Structural & …, 2023 - nature.com
Synaptic complexes of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)
receptors (AMPARs) with auxiliary subunits mediate most excitatory neurotransmission and …
receptors (AMPARs) with auxiliary subunits mediate most excitatory neurotransmission and …
Molecular pathway and structural mechanism of human oncochannel TRPV6 inhibition by the phytocannabinoid tetrahydrocannabivarin
A Neuberger, YA Trofimov, MV Yelshanskaya… - Nature …, 2023 - nature.com
The calcium-selective oncochannel TRPV6 is an important driver of cell proliferation in
human cancers. Despite increasing interest of pharmacological research in developing …
human cancers. Despite increasing interest of pharmacological research in developing …
AMPA receptor structure and auxiliary subunits
A Kamalova, T Nakagawa - The Journal of physiology, 2021 - Wiley Online Library
Fast excitatory synaptic transmission in the mammalian brain is largely mediated by AMPA‐
type ionotropic glutamate receptors (AMPARs), which are activated by the neurotransmitter …
type ionotropic glutamate receptors (AMPARs), which are activated by the neurotransmitter …
Structural mechanism of human oncochannel TRPV6 inhibition by the natural phytoestrogen genistein
A Neuberger, YA Trofimov, MV Yelshanskaya… - Nature …, 2023 - nature.com
Calcium-selective oncochannel TRPV6 is the major driver of cell proliferation in human
cancers. While significant effort has been invested in the development of synthetic TRPV6 …
cancers. While significant effort has been invested in the development of synthetic TRPV6 …