DocumentCode :
592390
Title :
Fold-change detection as a chemotaxis model discrimination tool
Author :
Hamadeh, Abdullah ; Ingalls, Brian ; Sontag, Eduardo
Author_Institution :
Dept. of Appl. Math., Univ. of Waterloo, Waterloo, ON, Canada
fYear :
2012
fDate :
10-13 Dec. 2012
Firstpage :
5523
Lastpage :
5527
Abstract :
Fold-change detection (FCD) is the property that a dynamical system with an adapting output will exhibit identical transient output responses when its input signals are scaled. This feature was recently demonstrated in the chemotactic response of the bacterium Escherichia coli, confirming earlier theoretical predictions. The chemotaxis pathway of the bacterium Rhodobacter sphaeroides has the same modular structure as that in E. coli but is significantly more complex in that it has multiple homologues of the latter´s chemotaxis proteins and features two, rather than one, chemosensory cluster. Recent experimental results suggest that R. sphaeroides may also exhibit FCD. In this paper, we present a set of theoretical assumptions on the dynamics of the R. sphaeroides chemosensory system, and use these to fit an integrated chemotaxis model to experimental data. We then show that the assumptions we place are sufficient to make FCD a robust property of this chemotaxis pathway, in agreement with preliminary experimental evidence. We argue that the fact that the model we present here is able to reproduce this transient dynamic property whilst earlier models cannot makes FCD a useful tool for model discrimination on the basis of transient dynamic response. This is in contrast to earlier model discrimination methods which tested the validity of models based on their ability to reproduce a finite set of experimental data. Further experiments that can provide additional validation of our theoretical assumptions are suggested.
Keywords :
cell motility; cellular biophysics; set theory; transient response; E. coli; FCD; R. sphaeroides chemosensory system; bacterium escherichia coli; bacterium rhodobacter sphaeroides; chemosensory cluster; chemotactic response; chemotaxis model discrimination tool; chemotaxis pathway; chemotaxis proteins; dynamical system; experimental data finite set; fold-change detection; identical transient output responses; integrated chemotaxis model; model discrimination methods; modular structure; transient dynamic property; transient dynamic response; Adaptation models; Approximation methods; Biological system modeling; Mathematical model; Microorganisms; Proteins; Steady-state;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Decision and Control (CDC), 2012 IEEE 51st Annual Conference on
Conference_Location :
Maui, HI
ISSN :
0743-1546
Print_ISBN :
978-1-4673-2065-8
Electronic_ISBN :
0743-1546
Type :
conf
DOI :
10.1109/CDC.2012.6426531
Filename :
6426531
Link To Document :
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