Evidence map›Paper›PMID 24580139›Full record

ArticleBiochemistry2014

New insights into bacterial chemoreceptor array structure and assembly from electron cryotomography.

Ariane Briegel, Margaret L Wong, Heather L Hodges, Catherine M Oikonomou, Kene N Piasta, Michael J Harris, Daniel J Fowler, Lynmarie K Thompson, Joseph J Falke, Laura L Kiessling and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Biochemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Distinct roles of PilI and ChpC inApplied and environmental microbiology · 2026
    Article
  2. Structure and signaling mechanism ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Microorganisms · 2025
    Review
  5. Insights into Chemoreceptor MCP2201-Sensing D-Malate.International journal of molecular sciences · 2025
    Article
  6. Article
  7. Bacterial chemoreceptor signaling complexes control kinase activity by stabilizing the catalytic domain of CheA.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Review
  9. Article
  10. Recent structural advances in bacterial chemotaxis signalling.Current opinion in structural biology · 2023
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Studying bacterial chemosensory array with CryoEM.Biochemical Society transactions · 2021
    Review
  16. Towards the Idea of Molecular Brains.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Cryogenic single-molecule fluorescence annotations for electron tomography reveal in situ organization of key proteins inProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  20. Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

11 authors.

Ariane BriegelDivision of Biology, California Institute of Technology , 1200 East California Boulevard, Pasadena, California 91125, United States.
Margaret L Wong
Heather L Hodges
Catherine M Oikonomou
Kene N Piasta
Michael J Harris
Daniel J Fowler
Lynmarie K Thompson
Joseph J Falke
Laura L Kiessling
Grant J Jensen

Funding

Chemistry-Biology Interface Training ProgramT32GM008505 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI BLACKWELL, HELEN E. · 1993 to 2023
$9.8M
CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAINING GRANTST32GM008515 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 1995 to 2020
$4.3M
MULTIVALENT PROTEIN CARBOHYDRATE INTERACTIONSR01GM055984 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI KIESSLING, LAURA L · 1997 to 2014
$3.9M
RECEPTORS &SIGNALING PROTEINS--DYNAMICS &ACTIVATIONR01GM040731 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI FALKE, JOSEPH J · 1988 to 2013
$3.4M
Assembly and Function of Bacterial Chemotaxis Receptor Signaling ComplexesR01GM085288 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 2010 to 2013
$1.2M
Structural Basis of ChemoreceptionR01GM101425 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI JENSEN, GRANT J · 2013 to 2016
$1.1M
NIGMS NIH HHS GM101425NIGMS NIH HHS R01 GM040731NIGMS NIH HHS R01-GM040731NIGMS NIH HHS R01 GM055984NIGMS NIH HHS R01-GM055984NIGMS NIH HHS R01 GM085288NIGMS NIH HHS R01-GM085288NIGMS NIH HHS R01 GM101425NIGMS NIH HHS T32 GM008505NIGMS NIH HHS T32 GM008515
6 · The paper itself

Abstract

Bacterial chemoreceptors cluster in highly ordered, cooperative, extended arrays with a conserved architecture, but the principles that govern array assembly remain unclear. Here we show images of cellular arrays as well as selected chemoreceptor complexes reconstituted in vitro that reveal new principles of array structure and assembly. First, in every case, receptors clustered in a trimers-of-dimers configuration, suggesting this is a highly favored fundamental building block. Second, these trimers-of-receptor dimers exhibited great versatility in the kinds of contacts they formed with each other and with other components of the signaling pathway, although only one architectural type occurred in native arrays. Third, the membrane, while it likely accelerates the formation of arrays, was neither necessary nor sufficient for lattice formation. Molecular crowding substituted for the stabilizing effect of the membrane and allowed cytoplasmic receptor fragments to form sandwiched lattices that strongly resemble the cytoplasmic chemoreceptor arrays found in some bacterial species. Finally, the effective determinant of array structure seemed to be CheA and CheW, which formed a "superlattice" of alternating CheA-filled and CheA-empty rings that linked receptor trimers-of-dimer units into their native hexagonal lattice. While concomitant overexpression of receptors, CheA, and CheW yielded arrays with native spacing, the CheA occupancy was lower and less ordered, suggesting that temporal and spatial coordination of gene expression driven by a single transcription factor may be vital for full order, or that array overgrowth may trigger a disassembly process. The results described here provide new insights into the assembly intermediates and assembly mechanism of this massive macromolecular complex.

Indexed as

Bacterial ProteinsChemotaxisCryoelectron MicroscopyElectronsEscherichia coliEscherichia coli ProteinsHistidine KinaseMembrane ProteinsMethyl-Accepting Chemotaxis ProteinsModels, MolecularProtein BindingBacterial ProteinscheA protein, E coliCheW protein, E coliEscherichia coli ProteinsHistidine KinaseMembrane ProteinsMethyl-Accepting Chemotaxis Proteins

Identifiers

PMID24580139
PMCPMC3985956

What OpenQuestion holds

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Registered trials

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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.