Evidence map›Paper›PMID 38076818›Full record

ArticlebioRxiv : the preprint server for biology2023

Allosteric Competition and Inhibition in AMPA Receptors.

W Dylan Hale, Alejandra Montaño Romero, Cuauhtemoc U Gonzalez, Vasanthi Jayaraman, Albert Y Lau, Richard L Huganir, Edward C Twomey

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

W Dylan HaleSolomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD USA.ORCID 0000-0002-1492-0735
Alejandra Montaño RomeroSolomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD USA.
Cuauhtemoc U GonzalezCenter for Membrane Biology, Department of Biochemistry and Molecular Biology, University of Texas Health Science Center at Houston, TX, USA.
Vasanthi JayaramanCenter for Membrane Biology, Department of Biochemistry and Molecular Biology, University of Texas Health Science Center at Houston, TX, USA.
Albert Y LauDepartment of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD USA.
Richard L HuganirSolomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD USA.ORCID 0000-0001-9783-5183
Edward C TwomeySolomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD USA.ORCID 0000-0002-1855-1586
Johns Hopkins University · USThe University of Texas Health Science Center at Houston · USThe University of Texas MD Anderson Cancer Center · US

Funding

PDZ DOMAINS AND EXCITATORY SYNAPTIC FUNCTIONR01NS036715 · NINDS · JOHNS HOPKINS UNIVERSITY · PI HUGANIR, RICHARD L · 1997 to 2020
$8.6M
Dynamics Of Ligand Gated Ion ChannelsR35GM122528 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Vasanthi Jayaraman · 2017 to 2026
$6.2M
Long-Lived Synaptic ProteinsR01MH112152 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HUGANIR, RICHARD L · 2017 to 2021
$2.9M
Structural dynamics and function of the glutamate receptor ligand-binding domainR01GM094495 · NIGMS · UNIVERSITY OF CHICAGO · PI LAU, ALBERT Y · 2010 to 2013
$1.0M
Structure-guided functional analysis of GluA4-NPTX2 interaction during PVIN homeostatic scalingK99MH132811 · NIMH · JOHNS HOPKINS UNIVERSITY · PI HALE, WILLIAM DYLAN · 2023 to 2024
$206k
Synaptic Organization and Modulation of Kainate Receptors: Investigating the Structure, Dynamics, and Function in the Context of Trans-Synaptic JunctionsF99NS130928 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI GONZALEZ, CUAUHTEMOC ULISES · 2023 to 2024
$75k
NIGMS NIH HHS R01 GM094495NIGMS NIH HHS R35 GM122528NIMH NIH HHS K99 MH132811NIMH NIH HHS R01 MH112152NINDS NIH HHS F99 NS130928NINDS NIH HHS R01 NS036715
6 · The paper itself

Abstract

Excitatory neurotransmission is principally mediated by AMPA-subtype ionotropic glutamate receptors (AMPARs). Dysregulation of AMPARs is the cause of many neurological disorders and how therapeutic candidates such as negative allosteric modulators inhibit AMPARs is unclear. Here, we show that non-competitive inhibition desensitizes AMPARs to activation and prevents positive allosteric modulation. We dissected the noncompetitive inhibition mechanism of action by capturing AMPARs bound to glutamate and the prototypical negative allosteric modulator, GYKI-52466, with cryo-electron microscopy. Noncompetitive inhibition by GYKI-52466, which binds in the transmembrane collar region surrounding the ion channel, negatively modulates AMPARs by decoupling glutamate binding in the ligand binding domain from the ion channel. Furthermore, during allosteric competition between negative and positive modulators, negative allosteric modulation by GKYI-52466 outcompetes positive allosteric modulators to control AMPAR function. Our data provide a new framework for understanding allostery of AMPARs and foundations for rational design of therapeutics targeting AMPARs in neurological diseases.

Identifiers

PMID38076818
PMCPMC10705377
OpenAlexW4389108301

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.