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Effective Biophysical Modeling of Cell Free Transcription and Translation Processes
Transcription and translation are at the heart of metabolism and signal transduction. In this study, we developed an effective biophysical modeling approach to simulate transcription and translation processes. The model, composed of coupled ordinary differential equations, was tested by comparing si...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726328/ https://www.ncbi.nlm.nih.gov/pubmed/33324619 http://dx.doi.org/10.3389/fbioe.2020.539081 |
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author | Adhikari, Abhinav Vilkhovoy, Michael Vadhin, Sandra Lim, Ha Eun Varner, Jeffrey D. |
author_facet | Adhikari, Abhinav Vilkhovoy, Michael Vadhin, Sandra Lim, Ha Eun Varner, Jeffrey D. |
author_sort | Adhikari, Abhinav |
collection | PubMed |
description | Transcription and translation are at the heart of metabolism and signal transduction. In this study, we developed an effective biophysical modeling approach to simulate transcription and translation processes. The model, composed of coupled ordinary differential equations, was tested by comparing simulations of two cell free synthetic circuits with experimental measurements generated in this study. First, we considered a simple circuit in which sigma factor 70 induced the expression of green fluorescent protein. This relatively simple case was then followed by a more complex negative feedback circuit in which two control genes were coupled to the expression of a third reporter gene, green fluorescent protein. Many of the model parameters were estimated from previous biophysical studies in the literature, while the remaining unknown model parameters for each circuit were estimated by minimizing the difference between model simulations and messenger RNA (mRNA) and protein measurements generated in this study. In particular, either parameter estimates from published studies were used directly, or characteristic values found in the literature were used to establish feasible ranges for the parameter estimation problem. In order to perform a detailed analysis of the influence of individual model parameters on the expression dynamics of each circuit, global sensitivity analysis was used. Taken together, the effective biophysical modeling approach captured the expression dynamics, including the transcription dynamics, for the two synthetic cell free circuits. While, we considered only two circuits here, this approach could potentially be extended to simulate other genetic circuits in both cell free and whole cell biomolecular applications as the equations governing the regulatory control functions are modular and easily modifiable. The model code, parameters, and analysis scripts are available for download under an MIT software license from the Varnerlab GitHub repository. |
format | Online Article Text |
id | pubmed-7726328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77263282020-12-14 Effective Biophysical Modeling of Cell Free Transcription and Translation Processes Adhikari, Abhinav Vilkhovoy, Michael Vadhin, Sandra Lim, Ha Eun Varner, Jeffrey D. Front Bioeng Biotechnol Bioengineering and Biotechnology Transcription and translation are at the heart of metabolism and signal transduction. In this study, we developed an effective biophysical modeling approach to simulate transcription and translation processes. The model, composed of coupled ordinary differential equations, was tested by comparing simulations of two cell free synthetic circuits with experimental measurements generated in this study. First, we considered a simple circuit in which sigma factor 70 induced the expression of green fluorescent protein. This relatively simple case was then followed by a more complex negative feedback circuit in which two control genes were coupled to the expression of a third reporter gene, green fluorescent protein. Many of the model parameters were estimated from previous biophysical studies in the literature, while the remaining unknown model parameters for each circuit were estimated by minimizing the difference between model simulations and messenger RNA (mRNA) and protein measurements generated in this study. In particular, either parameter estimates from published studies were used directly, or characteristic values found in the literature were used to establish feasible ranges for the parameter estimation problem. In order to perform a detailed analysis of the influence of individual model parameters on the expression dynamics of each circuit, global sensitivity analysis was used. Taken together, the effective biophysical modeling approach captured the expression dynamics, including the transcription dynamics, for the two synthetic cell free circuits. While, we considered only two circuits here, this approach could potentially be extended to simulate other genetic circuits in both cell free and whole cell biomolecular applications as the equations governing the regulatory control functions are modular and easily modifiable. The model code, parameters, and analysis scripts are available for download under an MIT software license from the Varnerlab GitHub repository. Frontiers Media S.A. 2020-11-26 /pmc/articles/PMC7726328/ /pubmed/33324619 http://dx.doi.org/10.3389/fbioe.2020.539081 Text en Copyright © 2020 Adhikari, Vilkhovoy, Vadhin, Lim and Varner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Adhikari, Abhinav Vilkhovoy, Michael Vadhin, Sandra Lim, Ha Eun Varner, Jeffrey D. Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title | Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title_full | Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title_fullStr | Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title_full_unstemmed | Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title_short | Effective Biophysical Modeling of Cell Free Transcription and Translation Processes |
title_sort | effective biophysical modeling of cell free transcription and translation processes |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726328/ https://www.ncbi.nlm.nih.gov/pubmed/33324619 http://dx.doi.org/10.3389/fbioe.2020.539081 |
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