Evidence map›Paper›PMID 24043807›Full record

ReviewProceedings of the National Academy of Sciences of the United States of America2013

A gating mechanism of pentameric ligand-gated ion channels.

Nicolas Calimet, Manuel Simoes, Jean-Pierre Changeux, Martin Karplus, Antoine Taly, Marco Cecchini

Open access · bronzeAbstract readReview
In one paragraph

Review in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
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

77 citing papers in PubMed, 149 citations in OpenAlex.

  1. Article
  2. Review
  3. Dynamics and Interplay of the Binding Pockets in the Glycine Receptor.Journal of chemical information and modeling · 2025
    Article
  4. Article
  5. Hidden complexity of α7 nicotinic acetylcholine receptor desensitization revealed by MD simulations and Markov state modeling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Phenols and GABAFrontiers in pharmacology · 2024
    Review
  13. Article
  14. Article
  15. Allosteric modulation of α1β3γ2 GABABiophysical journal · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. αACS chemical neuroscience · 2022
    Article
  20. Article

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Nicolas CalimetInstitut de Science et d'Ingénierie Supramoléculaires, Unité Mixte de Recherche 7006, Centre National de la Recherche Scientifique, Université de Strasbourg, F-67083 Strasbourg Cedex, France.
Manuel Simoes
Jean-Pierre Changeux
Martin Karplus
Antoine Taly
Marco Cecchini
Université de Strasbourg · FRCollège de France · FRHarvard University · USUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pentameric ligand-gated ion channels (pLGICs) play a central role in intercellular communication in the nervous system and are involved in fundamental processes such as attention, learning, and memory. They are oligomeric protein assemblies that convert a chemical signal into an ion flux through the postsynaptic membrane, but the molecular mechanism of gating ions has remained elusive. Here, we present atomistic molecular dynamics simulations of the prokaryotic channels from Gloeobacter violaceus (GLIC) and Erwinia chrysanthemi (ELIC), whose crystal structures are thought to represent the active and the resting states of pLGICs, respectively, and of the eukaryotic glutamate-gated chloride channel from Caenorhabditis elegans (GluCl), whose open-channel structure was determined complexed with the positive allosteric modulator ivermectin. Structural observables extracted from the trajectories of GLIC and ELIC are used as progress variables to analyze the time evolution of GluCl, which was simulated in the absence of ivermectin starting from the structure with bound ivermectin. The trajectory of GluCl with ivermectin removed shows a sequence of structural events that couple agonist unbinding from the extracellular domain to ion-pore closing in the transmembrane domain. Based on these results, we propose a structural mechanism for the allosteric communication leading to deactivation/activation of the GluCl channel. This model of gating emphasizes the coupling between the quaternary twisting and the opening/closing of the ion pore and is likely to apply to other members of the pLGIC family.

Indexed as

Ligand-Gated Ion ChannelsNerve Tissue ProteinsNeurotransmitter AgentsAnimalsHumansIon Channel GatingProtein Structure, SecondaryProtein Structure, TertiaryStructure-Activity RelationshipLigand-Gated Ion ChannelsNerve Tissue ProteinsNeurotransmitter Agentschemo-electrical transductionion channel gatingneurotransmitter receptors

Identifiers

PMID24043807
PMCPMC3801054
OpenAlexW1950332654

What OpenQuestion holds

Textmetadata
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.