Evidence map›Paper›PMID 19805102›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Universal architecture of bacterial chemoreceptor arrays.

Ariane Briegel, Davi R Ortega, Elitza I Tocheva, Kristin Wuichet, Zhuo Li, Songye Chen, Axel Müller, Cristina V Iancu, Gavin E Murphy, Megan J Dobro and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 203 papers.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed
15.4field-weighted citation impact, top 1% 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

203 citing papers in PubMed, 325 citations in OpenAlex.

  1. Distinct roles of PilI and ChpC inApplied and environmental microbiology · 2026
    Article
  2. Article
  3. Article
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  5. Review
  6. Nature physics · 2026
    Article
  7. Microorganisms · 2025
    Review
  8. ChemotaxingbioRxiv : the preprint server for biology · 2025
    Article
  9. ChemotaxingArXiv · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The exceptional form and function of the giant bacteriumProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. Article
  19. A nonequilibrium allosteric model for receptor-kinase complexes: The role of energy dissipation in chemotaxis signaling.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  20. Article

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

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

12 authors at 7 institutions in 1 country.

Ariane BriegelDivisions of Biology and Howard Hughes Medical Institute, California Institute of Technology, Pasadena, CA 91125, USA.
Davi R Ortega
Elitza I Tocheva
Kristin Wuichet
Zhuo Li
Songye Chen
Axel Müller
Cristina V Iancu
Gavin E Murphy
Megan J Dobro
Igor B Zhulin
Grant J Jensen
National Cancer Institute · USCenter for Cancer Research · USUniversity of Tennessee at Knoxville · USCalifornia Institute of Technology · USHoward Hughes Medical Institute · USNational Institutes of Health · USOak Ridge National Laboratory · US

Funding

X-ray Cryst. CoreP50GM082545 · NIGMS · UNIVERSITY OF UTAH · PI SUNDQUIST, WESLEY I. · 2007 to 2018
$51.1M
Computational Genomics of Signal TransductionR01GM072285 · NIGMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI JOULINE, IGOR B. · 2004 to 2018
$3.2M
Structure and function of the prokaryotic cytoskeleton by electron cryotomographyR01AI067548 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI JENSEN, GRANT J · 2006 to 2010
$1.6M
Howard Hughes Medical InstituteNIAID NIH HHS R01 AI067548NIGMS NIH HHS P50 GM082545NIGMS NIH HHS R01 GM072285NIGMS NIH HHS R01 GM72285
6 · The paper itself

Abstract

Chemoreceptors are key components of the high-performance signal transduction system that controls bacterial chemotaxis. Chemoreceptors are typically localized in a cluster at the cell pole, where interactions among the receptors in the cluster are thought to contribute to the high sensitivity, wide dynamic range, and precise adaptation of the signaling system. Previous structural and genomic studies have produced conflicting models, however, for the arrangement of the chemoreceptors in the clusters. Using whole-cell electron cryo-tomography, here we show that chemoreceptors of different classes and in many different species representing several major bacterial phyla are all arranged into a highly conserved, 12-nm hexagonal array consistent with the proposed "trimer of dimers" organization. The various observed lengths of the receptors confirm current models for the methylation, flexible bundle, signaling, and linker sub-domains in vivo. Our results suggest that the basic mechanism and function of receptor clustering is universal among bacterial species and was thus conserved during evolution.

Indexed as

PhylogenyBacteriaBacterial ProteinsCaulobacter crescentusCryoelectron MicroscopyDatabases, GeneticElectron Microscope TomographyEscherichia coliEvolution, MolecularGenome, BacterialMembrane ProteinsMethyl-Accepting Chemotaxis ProteinsThermotoga maritimaBacterial ProteinsMembrane ProteinsMethyl-Accepting Chemotaxis Proteins

Identifiers

PMID19805102
PMCPMC2761316
OpenAlexW2137365831

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.