Evidence map›Paper›PMID 20485527›Full record

ArticlePloS one2010

An agent-based model of signal transduction in bacterial chemotaxis.

Jameson Miller, Miles Parker, Robert B Bourret, Morgan C Giddings

Abstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Agent-Based Modeling of T Cell Receptor Cooperativity.International journal of molecular sciences · 2020
    Article
  4. Article
  5. Article
  6. Article
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

4 authors.

Jameson MillerDepartment of Computer Science, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Miles Parker
Robert B Bourret
Morgan C Giddings

Funding

Molecular Mechanisms of Signal Transduction by Two-Component Regulatory SystemsR01GM050860 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOURRET, ROBERT B. · 1994 to 2025
$7.9M
Developing Software For Protein-Based Gene FindingR01HG003700 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GIDDINGS, MORGAN CORINNE · 2005 to 2011
$3.3M
Software to Identify Post-translational Modifications From Proteomic Data SetsR01RR020823 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GIDDINGS, MORGAN CORINNE · 2004 to 2011
$2.6M
NCRR NIH HHS R01 RR020823NCRR NIH HHS RR020823NHGRI NIH HHS HG003700NHGRI NIH HHS R01 HG003700NIGMS NIH HHS GM050860NIGMS NIH HHS R01 GM050860
6 · The paper itself

Abstract

We report the application of agent-based modeling to examine the signal transduction network and receptor arrays for chemotaxis in Escherichia coli, which are responsible for regulating swimming behavior in response to environmental stimuli. Agent-based modeling is a stochastic and bottom-up approach, where individual components of the modeled system are explicitly represented, and bulk properties emerge from their movement and interactions. We present the Chemoscape model: a collection of agents representing both fixed membrane-embedded and mobile cytoplasmic proteins, each governed by a set of rules representing knowledge or hypotheses about their function. When the agents were placed in a simulated cellular space and then allowed to move and interact stochastically, the model exhibited many properties similar to the biological system including adaptation, high signal gain, and wide dynamic range. We found the agent based modeling approach to be both powerful and intuitive for testing hypotheses about biological properties such as self-assembly, the non-linear dynamics that occur through cooperative protein interactions, and non-uniform distributions of proteins in the cell. We applied the model to explore the role of receptor type, geometry and cooperativity in the signal gain and dynamic range of the chemotactic response to environmental stimuli. The model provided substantial qualitative evidence that the dynamic range of chemotactic response can be traced to both the heterogeneity of receptor types present, and the modulation of their cooperativity by their methylation state.

Indexed as

ChemotaxisModels, BiologicalSignal TransductionChemoreceptor CellsComputer SimulationEscherichia coliEscherichia coli ProteinsLigandsMethylationProtein MultimerizationReceptors, Cell SurfaceEscherichia coli ProteinsLigandsReceptors, Cell SurfaceTar protein, E coli

Identifiers

PMID20485527
PMCPMC2869346

What OpenQuestion holds

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LicenceCC BY
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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.