Cargando…
Evolving cell models for systems and synthetic biology
This paper proposes a new methodology for the automated design of cell models for systems and synthetic biology. Our modelling framework is based on P systems, a discrete, stochastic and modular formal modelling language. The automated design of biological models comprising the optimization of the m...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816226/ https://www.ncbi.nlm.nih.gov/pubmed/20186253 http://dx.doi.org/10.1007/s11693-009-9050-7 |
_version_ | 1782177081580322816 |
---|---|
author | Cao, Hongqing Romero-Campero, Francisco J. Heeb, Stephan Cámara, Miguel Krasnogor, Natalio |
author_facet | Cao, Hongqing Romero-Campero, Francisco J. Heeb, Stephan Cámara, Miguel Krasnogor, Natalio |
author_sort | Cao, Hongqing |
collection | PubMed |
description | This paper proposes a new methodology for the automated design of cell models for systems and synthetic biology. Our modelling framework is based on P systems, a discrete, stochastic and modular formal modelling language. The automated design of biological models comprising the optimization of the model structure and its stochastic kinetic constants is performed using an evolutionary algorithm. The evolutionary algorithm evolves model structures by combining different modules taken from a predefined module library and then it fine-tunes the associated stochastic kinetic constants. We investigate four alternative objective functions for the fitness calculation within the evolutionary algorithm: (1) equally weighted sum method, (2) normalization method, (3) randomly weighted sum method, and (4) equally weighted product method. The effectiveness of the methodology is tested on four case studies of increasing complexity including negative and positive autoregulation as well as two gene networks implementing a pulse generator and a bandwidth detector. We provide a systematic analysis of the evolutionary algorithm’s results as well as of the resulting evolved cell models. |
format | Text |
id | pubmed-2816226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-28162262010-02-13 Evolving cell models for systems and synthetic biology Cao, Hongqing Romero-Campero, Francisco J. Heeb, Stephan Cámara, Miguel Krasnogor, Natalio Syst Synth Biol Research Article This paper proposes a new methodology for the automated design of cell models for systems and synthetic biology. Our modelling framework is based on P systems, a discrete, stochastic and modular formal modelling language. The automated design of biological models comprising the optimization of the model structure and its stochastic kinetic constants is performed using an evolutionary algorithm. The evolutionary algorithm evolves model structures by combining different modules taken from a predefined module library and then it fine-tunes the associated stochastic kinetic constants. We investigate four alternative objective functions for the fitness calculation within the evolutionary algorithm: (1) equally weighted sum method, (2) normalization method, (3) randomly weighted sum method, and (4) equally weighted product method. The effectiveness of the methodology is tested on four case studies of increasing complexity including negative and positive autoregulation as well as two gene networks implementing a pulse generator and a bandwidth detector. We provide a systematic analysis of the evolutionary algorithm’s results as well as of the resulting evolved cell models. Springer Netherlands 2010-01-22 2010-03 /pmc/articles/PMC2816226/ /pubmed/20186253 http://dx.doi.org/10.1007/s11693-009-9050-7 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Research Article Cao, Hongqing Romero-Campero, Francisco J. Heeb, Stephan Cámara, Miguel Krasnogor, Natalio Evolving cell models for systems and synthetic biology |
title | Evolving cell models for systems and synthetic biology |
title_full | Evolving cell models for systems and synthetic biology |
title_fullStr | Evolving cell models for systems and synthetic biology |
title_full_unstemmed | Evolving cell models for systems and synthetic biology |
title_short | Evolving cell models for systems and synthetic biology |
title_sort | evolving cell models for systems and synthetic biology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816226/ https://www.ncbi.nlm.nih.gov/pubmed/20186253 http://dx.doi.org/10.1007/s11693-009-9050-7 |
work_keys_str_mv | AT caohongqing evolvingcellmodelsforsystemsandsyntheticbiology AT romerocamperofranciscoj evolvingcellmodelsforsystemsandsyntheticbiology AT heebstephan evolvingcellmodelsforsystemsandsyntheticbiology AT camaramiguel evolvingcellmodelsforsystemsandsyntheticbiology AT krasnogornatalio evolvingcellmodelsforsystemsandsyntheticbiology |