Leveraging the model-experiment loop: Examples from cellular slime mold chemotaxis.

Cellular slime mold Chemotaxis Dictyostelium Model-experiment interplay Modeling Simulations

Journal

Experimental cell research
ISSN: 1090-2422
Titre abrégé: Exp Cell Res
Pays: United States
ID NLM: 0373226

Informations de publication

Date de publication:
01 09 2022
Historique:
received: 25 02 2022
accepted: 19 05 2022
pubmed: 27 5 2022
medline: 20 7 2022
entrez: 26 5 2022
Statut: ppublish

Résumé

Interplay between models and experimental data advances discovery and understanding in biology, particularly when models generate predictions that allow well-designed experiments to distinguish between alternative mechanisms. To illustrate how this feedback between models and experiments can lead to key insights into biological mechanisms, we explore three examples from cellular slime mold chemotaxis. These examples include studies that identified chemotaxis as the primary mechanism behind slime mold aggregation, discovered that cells likely measure chemoattractant gradients by sensing concentration differences across cell length, and tested the role of cell-associated chemoattractant degradation in shaping chemotactic fields. Although each study used a different model class appropriate to their hypotheses - qualitative, mathematical, or simulation-based - these examples all highlight the utility of modeling to formalize assumptions and generate testable predictions. A central element of this framework is the iterative use of models and experiments, specifically: matching experimental designs to the models, revising models based on mismatches with experimental data, and validating critical model assumptions and predictions with experiments. We advocate for continued use of this interplay between models and experiments to advance biological discovery.

Identifiants

pubmed: 35618013
pii: S0014-4827(22)00211-7
doi: 10.1016/j.yexcr.2022.113218
pii:
doi:

Substances chimiques

Chemotactic Factors 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113218

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM133616
Pays : United States

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Xinwen Zhu (X)

Department of Biomedical Engineering and the Biological Design Center, Boston University, Boston, MA 02215, USA.

Emily R Hager (ER)

Department of Biomedical Engineering and the Biological Design Center, Boston University, Boston, MA 02215, USA.

Chuqiao Huyan (C)

Department of Biomedical Engineering and the Biological Design Center, Boston University, Boston, MA 02215, USA.

Allyson E Sgro (AE)

Department of Biomedical Engineering and the Biological Design Center, Boston University, Boston, MA 02215, USA. Electronic address: asgro@bu.edu.

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Classifications MeSH