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Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells
Quantitative modeling is useful for predicting behaviors of a system and for rationally constructing or modifying the system. The predictive power of a model relies on accurate quantification of model parameters. Here, we illustrate challenges in parameter quantification and offer means to overcome...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402699/ https://www.ncbi.nlm.nih.gov/pubmed/30794534 http://dx.doi.org/10.1371/journal.pbio.3000135 |
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author | Hart, Samuel F. M. Mi, Hanbing Green, Robin Xie, Li Pineda, Jose Mario Bello Momeni, Babak Shou, Wenying |
author_facet | Hart, Samuel F. M. Mi, Hanbing Green, Robin Xie, Li Pineda, Jose Mario Bello Momeni, Babak Shou, Wenying |
author_sort | Hart, Samuel F. M. |
collection | PubMed |
description | Quantitative modeling is useful for predicting behaviors of a system and for rationally constructing or modifying the system. The predictive power of a model relies on accurate quantification of model parameters. Here, we illustrate challenges in parameter quantification and offer means to overcome these challenges, using a case example in which we quantitatively predict the growth rate of a cooperative community. Specifically, the community consists of two Saccharomyces cerevisiae strains, each engineered to release a metabolite required and consumed by its partner. The initial model, employing parameters measured in batch monocultures with zero or excess metabolite, failed to quantitatively predict experimental results. To resolve the model–experiment discrepancy, we chemically identified the correct exchanged metabolites, but this did not improve model performance. We then remeasured strain phenotypes in chemostats mimicking the metabolite-limited community environments, while mitigating or incorporating effects of rapid evolution. Almost all phenotypes we measured, including death rate, metabolite release rate, and the amount of metabolite consumed per cell birth, varied significantly with the metabolite environment. Once we used parameters measured in a range of community-like chemostat environments, prediction quantitatively agreed with experimental results. In summary, using a simplified community, we uncovered and devised means to resolve modeling challenges that are likely general to living systems. |
format | Online Article Text |
id | pubmed-6402699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64026992019-03-17 Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells Hart, Samuel F. M. Mi, Hanbing Green, Robin Xie, Li Pineda, Jose Mario Bello Momeni, Babak Shou, Wenying PLoS Biol Research Article Quantitative modeling is useful for predicting behaviors of a system and for rationally constructing or modifying the system. The predictive power of a model relies on accurate quantification of model parameters. Here, we illustrate challenges in parameter quantification and offer means to overcome these challenges, using a case example in which we quantitatively predict the growth rate of a cooperative community. Specifically, the community consists of two Saccharomyces cerevisiae strains, each engineered to release a metabolite required and consumed by its partner. The initial model, employing parameters measured in batch monocultures with zero or excess metabolite, failed to quantitatively predict experimental results. To resolve the model–experiment discrepancy, we chemically identified the correct exchanged metabolites, but this did not improve model performance. We then remeasured strain phenotypes in chemostats mimicking the metabolite-limited community environments, while mitigating or incorporating effects of rapid evolution. Almost all phenotypes we measured, including death rate, metabolite release rate, and the amount of metabolite consumed per cell birth, varied significantly with the metabolite environment. Once we used parameters measured in a range of community-like chemostat environments, prediction quantitatively agreed with experimental results. In summary, using a simplified community, we uncovered and devised means to resolve modeling challenges that are likely general to living systems. Public Library of Science 2019-02-22 /pmc/articles/PMC6402699/ /pubmed/30794534 http://dx.doi.org/10.1371/journal.pbio.3000135 Text en © 2019 Hart et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hart, Samuel F. M. Mi, Hanbing Green, Robin Xie, Li Pineda, Jose Mario Bello Momeni, Babak Shou, Wenying Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title | Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title_full | Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title_fullStr | Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title_full_unstemmed | Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title_short | Uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
title_sort | uncovering and resolving challenges of quantitative modeling in a simplified community of interacting cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402699/ https://www.ncbi.nlm.nih.gov/pubmed/30794534 http://dx.doi.org/10.1371/journal.pbio.3000135 |
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