Evidence map›Paper›PMID 29491460›Full record

ArticleNature communications2018

High capacity in G protein-coupled receptor signaling.

Amiran Keshelava, Gonzalo P Solis, Micha Hersch, Alexey Koval, Mikhail Kryuchkov, Sven Bergmann, Vladimir L Katanaev

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 55 citations in OpenAlex.

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  2. Foods (Basel, Switzerland) · 2025
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  6. Information Transmission in G Protein-Coupled Receptors.International journal of molecular sciences · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Article
  18. The Effect of Deuteration on the HMolecules (Basel, Switzerland) · 2020
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Amiran KeshelavaDepartment of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland.
Gonzalo P SolisDepartment of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland.
Micha HerschDepartment of Computational Biology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland.
Alexey KovalDepartment of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland.
Mikhail KryuchkovDepartment of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland.
Sven BergmannDepartment of Computational Biology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland. sven.bergmann@unil.ch.ORCID http://orcid.org/0000-0002-6785-9034
Vladimir L KatanaevDepartment of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, 1011, Lausanne, Switzerland. vladimir.katanaev@unil.ch.
University of Lausanne · CHSIB Swiss Institute of Bioinformatics · CHFar Eastern Federal University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) constitute a large family of receptors that activate intracellular signaling pathways upon detecting specific extracellular ligands. While many aspects of GPCR signaling have been uncovered through decades of studies, some fundamental properties, like its channel capacity-a measure of how much information a given transmission system can reliably transduce-are still debated. Previous studies concluded that GPCRs in individual cells could transmit around one bit of information about the concentration of the ligands, allowing only for a reliable on or off response. Using muscarinic receptor-induced calcium response measured in individual cells upon repeated stimulation, we show that GPCR signaling systems possess a significantly higher capacity. We estimate the channel capacity of this system to be above two, implying that at least four concentration levels of the agonist can be distinguished reliably. These findings shed light on the basic principles of GPCR signaling.

Indexed as

AcetylcholineCalciumCell LineCell MembraneHEK293 CellsHumansMuscarinic AgonistsReceptor, Muscarinic M3Receptors, G-Protein-CoupledSignal TransductionAcetylcholineCalciumMuscarinic AgonistsReceptor, Muscarinic M3Receptors, G-Protein-Coupled

Identifiers

PMID29491460
PMCPMC5830429
OpenAlexW2794520513

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.