Dependence of bacterial chemotaxis on gradient shape and adaptation rate.

Simulation of cellular behavior on multiple scales requires models that are sufficiently detailed to capture central intracellular processes but at the same time enable the simulation of entire cell populations in a computationally cheap way. In this paper we present RapidCell, a hybrid model of che...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Nikita Vladimirov, Linda Løvdok, Dirk Lebiedz, Victor Sourjik
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2008
Materias:
Acceso en línea:https://doaj.org/article/152a31d2199648e1bf38e4254dbb9e08
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:152a31d2199648e1bf38e4254dbb9e08
record_format dspace
spelling oai:doaj.org-article:152a31d2199648e1bf38e4254dbb9e082021-11-25T05:41:55ZDependence of bacterial chemotaxis on gradient shape and adaptation rate.1553-734X1553-735810.1371/journal.pcbi.1000242https://doaj.org/article/152a31d2199648e1bf38e4254dbb9e082008-12-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19096502/?tool=EBIhttps://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Simulation of cellular behavior on multiple scales requires models that are sufficiently detailed to capture central intracellular processes but at the same time enable the simulation of entire cell populations in a computationally cheap way. In this paper we present RapidCell, a hybrid model of chemotactic Escherichia coli that combines the Monod-Wyman-Changeux signal processing by mixed chemoreceptor clusters, the adaptation dynamics described by ordinary differential equations, and a detailed model of cell tumbling. Our model dramatically reduces computational costs and allows the highly efficient simulation of E. coli chemotaxis. We use the model to investigate chemotaxis in different gradients, and suggest a new, constant-activity type of gradient to systematically study chemotactic behavior of virtual bacteria. Using the unique properties of this gradient, we show that optimal chemotaxis is observed in a narrow range of CheA kinase activity, where concentration of the response regulator CheY-P falls into the operating range of flagellar motors. Our simulations also confirm that the CheB phosphorylation feedback improves chemotactic efficiency by shifting the average CheY-P concentration to fit the motor operating range. Our results suggest that in liquid media the variability in adaptation times among cells may be evolutionary favorable to ensure coexistence of subpopulations that will be optimally tactic in different gradients. However, in a porous medium (agar) such variability appears to be less important, because agar structure poses mainly negative selection against subpopulations with low levels of adaptation enzymes. RapidCell is available from the authors upon request.Nikita VladimirovLinda LøvdokDirk LebiedzVictor SourjikPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 4, Iss 12, p e1000242 (2008)
institution DOAJ
collection DOAJ
language EN
topic Biology (General)
QH301-705.5
spellingShingle Biology (General)
QH301-705.5
Nikita Vladimirov
Linda Løvdok
Dirk Lebiedz
Victor Sourjik
Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
description Simulation of cellular behavior on multiple scales requires models that are sufficiently detailed to capture central intracellular processes but at the same time enable the simulation of entire cell populations in a computationally cheap way. In this paper we present RapidCell, a hybrid model of chemotactic Escherichia coli that combines the Monod-Wyman-Changeux signal processing by mixed chemoreceptor clusters, the adaptation dynamics described by ordinary differential equations, and a detailed model of cell tumbling. Our model dramatically reduces computational costs and allows the highly efficient simulation of E. coli chemotaxis. We use the model to investigate chemotaxis in different gradients, and suggest a new, constant-activity type of gradient to systematically study chemotactic behavior of virtual bacteria. Using the unique properties of this gradient, we show that optimal chemotaxis is observed in a narrow range of CheA kinase activity, where concentration of the response regulator CheY-P falls into the operating range of flagellar motors. Our simulations also confirm that the CheB phosphorylation feedback improves chemotactic efficiency by shifting the average CheY-P concentration to fit the motor operating range. Our results suggest that in liquid media the variability in adaptation times among cells may be evolutionary favorable to ensure coexistence of subpopulations that will be optimally tactic in different gradients. However, in a porous medium (agar) such variability appears to be less important, because agar structure poses mainly negative selection against subpopulations with low levels of adaptation enzymes. RapidCell is available from the authors upon request.
format article
author Nikita Vladimirov
Linda Løvdok
Dirk Lebiedz
Victor Sourjik
author_facet Nikita Vladimirov
Linda Løvdok
Dirk Lebiedz
Victor Sourjik
author_sort Nikita Vladimirov
title Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
title_short Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
title_full Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
title_fullStr Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
title_full_unstemmed Dependence of bacterial chemotaxis on gradient shape and adaptation rate.
title_sort dependence of bacterial chemotaxis on gradient shape and adaptation rate.
publisher Public Library of Science (PLoS)
publishDate 2008
url https://doaj.org/article/152a31d2199648e1bf38e4254dbb9e08
work_keys_str_mv AT nikitavladimirov dependenceofbacterialchemotaxisongradientshapeandadaptationrate
AT lindaløvdok dependenceofbacterialchemotaxisongradientshapeandadaptationrate
AT dirklebiedz dependenceofbacterialchemotaxisongradientshapeandadaptationrate
AT victorsourjik dependenceofbacterialchemotaxisongradientshapeandadaptationrate
_version_ 1718414501821284352