Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.

The ability of systems and synthetic biologists to observe the dynamics of cellular behavior is hampered by the limitations of the sensors, such as fluorescent proteins, available for use in time-lapse microscopy. In this paper, we propose a generalized solution to the problem of estimating the stat...

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Main Authors: David Thorsley, Eric Klavins
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3491022?pdf=render
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spelling doaj-b7de6135cb9640aa83d98a7438a2701e2020-11-25T01:17:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4715110.1371/journal.pone.0047151Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.David ThorsleyEric KlavinsThe ability of systems and synthetic biologists to observe the dynamics of cellular behavior is hampered by the limitations of the sensors, such as fluorescent proteins, available for use in time-lapse microscopy. In this paper, we propose a generalized solution to the problem of estimating the state of a stochastic chemical reaction network from limited sensor information generated by microscopy. We mathematically derive an observer structure for cells growing under time-lapse microscopy and incorporates the effects of cell division in order to estimate the dynamically-changing state of each cell in the colony. Furthermore, the observer can be used to discrimate between models by treating model indices as states whose values do not change with time. We derive necessary and sufficient conditions that specify when stochastic chemical reaction network models, interpreted as continuous-time Markov chains, can be distinguished from each other under both continual and periodic observation. We validate the performance of the observer on the Thattai-van Oudenaarden model of transcription and translation. The observer structure is most effective when the system model is well-parameterized, suggesting potential applications in synthetic biology where standardized biological parts are available. However, further research is necessary to develop computationally tractable approximations to the exact generalized solution presented here.http://europepmc.org/articles/PMC3491022?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author David Thorsley
Eric Klavins
spellingShingle David Thorsley
Eric Klavins
Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
PLoS ONE
author_facet David Thorsley
Eric Klavins
author_sort David Thorsley
title Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
title_short Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
title_full Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
title_fullStr Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
title_full_unstemmed Estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
title_sort estimation and discrimination of stochastic biochemical circuits from time-lapse microscopy data.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The ability of systems and synthetic biologists to observe the dynamics of cellular behavior is hampered by the limitations of the sensors, such as fluorescent proteins, available for use in time-lapse microscopy. In this paper, we propose a generalized solution to the problem of estimating the state of a stochastic chemical reaction network from limited sensor information generated by microscopy. We mathematically derive an observer structure for cells growing under time-lapse microscopy and incorporates the effects of cell division in order to estimate the dynamically-changing state of each cell in the colony. Furthermore, the observer can be used to discrimate between models by treating model indices as states whose values do not change with time. We derive necessary and sufficient conditions that specify when stochastic chemical reaction network models, interpreted as continuous-time Markov chains, can be distinguished from each other under both continual and periodic observation. We validate the performance of the observer on the Thattai-van Oudenaarden model of transcription and translation. The observer structure is most effective when the system model is well-parameterized, suggesting potential applications in synthetic biology where standardized biological parts are available. However, further research is necessary to develop computationally tractable approximations to the exact generalized solution presented here.
url http://europepmc.org/articles/PMC3491022?pdf=render
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