Evidence map›Paper›PMID 11390967›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Kinetic proofreading models for cell signaling predict ways to escape kinetic proofreading.

W S Hlavacek, A Redondo, H Metzger, C Wofsy, B Goldstein

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Tunable kinetic proofreading in a model with molecular frustration.Theory in biosciences = Theorie in den Biowissenschaften · 2012
    Article
  10. Review
  11. The Influence of Look-Ahead on the Error Rate of Transcription.Mathematical modelling of natural phenomena · 2010
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Stochastic models of receptor oligomerization by bivalent ligand.Journal of the Royal Society, Interface · 2006
    Article
  17. Article
  18. Article
  19. Signaling cascades: escape from kinetic proofreading.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Review
  20. Unexpected signals in a system subject to kinetic proofreading.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

W S HlavacekTheoretical Biology and Biophysics Group, Los Alamos National Laboratory, Los Alamos, NM 87545, USA.
A Redondo
H Metzger
C Wofsy
B Goldstein
Los Alamos National Laboratory · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · US

Funding

Receptor Aggregation and Its EffectsR37GM035556 · NIGMS · UNIVERSITY OF CALIF-LOS ALAMOS NAT LAB · PI GOLDSTEIN, BYRON B · 2003 to 2012
$6.4M
RECEPTOR AGGREGATION AND ITS EFFECTSR01GM035556 · NIGMS · UNIVERSITY OF CALIF-LOS ALAMOS NAT LAB · PI GOLDSTEIN, BYRON B · 1985 to 2002
$1.2M
CELL SURFACE RECEPTORS FOR IGEZ01AR041025 · NIAMS · ARTHRITIS, MUSCULOSKELETAL, SKIN DIS · PI METZGER, HENRY · 1986 to 2002
–
NIGMS NIH HHS GM35556NIGMS NIH HHS R01 GM035556NIGMS NIH HHS R37 GM035556
6 · The paper itself

Abstract

In the context of cell signaling, kinetic proofreading was introduced to explain how cells can discriminate among ligands based on a kinetic parameter, the ligand-receptor dissociation rate constant. In the kinetic proofreading model of cell signaling, responses occur only when a bound receptor undergoes a complete series of modifications. If the ligand dissociates prematurely, the receptor returns to its basal state and signaling is frustrated. We extend the model to deal with systems where aggregation of receptors is essential to signal transduction, and present a version of the model for systems where signaling depends on an extrinsic kinase. We also investigate the kinetics of signaling molecules, "messengers," that are generated by aggregated receptors but do not remain associated with the receptor complex. We show that the extended model predicts modes of signaling that exhibit kinetic discrimination for some range of parameters but for other parameter values show little or no discrimination and thus escape kinetic proofreading. We compare model predictions with experimental data.

Indexed as

AnimalsEnzyme PrecursorsIntracellular Signaling Peptides and ProteinsKineticsLeukemia, Basophilic, AcuteLigandsModels, BiologicalModels, TheoreticalPhosphorylationPhosphotyrosineProtein-Tyrosine KinasesRatsReceptors, CytokineReceptors, IgESignal Transductionsrc-Family KinasesEnzyme PrecursorsIntracellular Signaling Peptides and ProteinsLigandslyn protein-tyrosine kinasePhosphotyrosineProtein-Tyrosine KinasesReceptors, CytokineReceptors, IgEsrc-Family KinasesSyk KinaseSyk protein, ratTrans-Activators

Identifiers

PMID11390967
PMCPMC34662
OpenAlexW2118748684

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.