Cargando…
Computational analysis of viable parameter regions in models of synthetic biological systems
BACKGROUND: Gene regulatory networks with different topological and/or dynamical properties might exhibit similar behavior. System that is less perceptive for the perturbations of its internal and external factors should be preferred. Methods for sensitivity and robustness assessment have already be...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751877/ https://www.ncbi.nlm.nih.gov/pubmed/31548864 http://dx.doi.org/10.1186/s13036-019-0205-0 |
_version_ | 1783452704148815872 |
---|---|
author | Pušnik, žiga Mraz, Miha Zimic, Nikolaj Moškon, Miha |
author_facet | Pušnik, žiga Mraz, Miha Zimic, Nikolaj Moškon, Miha |
author_sort | Pušnik, žiga |
collection | PubMed |
description | BACKGROUND: Gene regulatory networks with different topological and/or dynamical properties might exhibit similar behavior. System that is less perceptive for the perturbations of its internal and external factors should be preferred. Methods for sensitivity and robustness assessment have already been developed and can be roughly divided into local and global approaches. Local methods focus only on the local area around nominal parameter values. This can be problematic when parameters exhibits the desired behavior over a large range of parameter perturbations or when parameter values are unknown. Global methods, on the other hand, investigate the whole space of parameter values and mostly rely on different sampling techniques. This can be computationally inefficient. To address these shortcomings ’glocal’ approaches were developed that apply global and local approaches in an effective and rigorous manner. RESULTS: Herein, we present a computational approach for ’glocal’ analysis of viable parameter regions in biological models. The methodology is based on the exploration of high-dimensional viable parameter spaces with global and local sampling, clustering and dimensionality reduction techniques. The proposed methodology allows us to efficiently investigate the viable parameter space regions, evaluate the regions which exhibit the largest robustness, and to gather new insights regarding the size and connectivity of the viable parameter regions. We evaluate the proposed methodology on three different synthetic gene regulatory network models, i.e. the repressilator model, the model of the AC-DC circuit and the model of the edge-triggered master-slave D flip-flop. CONCLUSIONS: The proposed methodology provides a rigorous assessment of the shape and size of viable parameter regions based on (1) the mathematical description of the biological system of interest, (2) constraints that define feasible parameter regions and (3) cost function that defines the desired or observed behavior of the system. These insights can be used to assess the robustness of biological systems, even in the case when parameter values are unknown and more importantly, even when there are multiple poorly connected viable parameter regions in the solution space. Moreover, the methodology can be efficiently applied to the analysis of biological systems that exhibit multiple modes of the targeted behavior. |
format | Online Article Text |
id | pubmed-6751877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67518772019-09-23 Computational analysis of viable parameter regions in models of synthetic biological systems Pušnik, žiga Mraz, Miha Zimic, Nikolaj Moškon, Miha J Biol Eng Methodology BACKGROUND: Gene regulatory networks with different topological and/or dynamical properties might exhibit similar behavior. System that is less perceptive for the perturbations of its internal and external factors should be preferred. Methods for sensitivity and robustness assessment have already been developed and can be roughly divided into local and global approaches. Local methods focus only on the local area around nominal parameter values. This can be problematic when parameters exhibits the desired behavior over a large range of parameter perturbations or when parameter values are unknown. Global methods, on the other hand, investigate the whole space of parameter values and mostly rely on different sampling techniques. This can be computationally inefficient. To address these shortcomings ’glocal’ approaches were developed that apply global and local approaches in an effective and rigorous manner. RESULTS: Herein, we present a computational approach for ’glocal’ analysis of viable parameter regions in biological models. The methodology is based on the exploration of high-dimensional viable parameter spaces with global and local sampling, clustering and dimensionality reduction techniques. The proposed methodology allows us to efficiently investigate the viable parameter space regions, evaluate the regions which exhibit the largest robustness, and to gather new insights regarding the size and connectivity of the viable parameter regions. We evaluate the proposed methodology on three different synthetic gene regulatory network models, i.e. the repressilator model, the model of the AC-DC circuit and the model of the edge-triggered master-slave D flip-flop. CONCLUSIONS: The proposed methodology provides a rigorous assessment of the shape and size of viable parameter regions based on (1) the mathematical description of the biological system of interest, (2) constraints that define feasible parameter regions and (3) cost function that defines the desired or observed behavior of the system. These insights can be used to assess the robustness of biological systems, even in the case when parameter values are unknown and more importantly, even when there are multiple poorly connected viable parameter regions in the solution space. Moreover, the methodology can be efficiently applied to the analysis of biological systems that exhibit multiple modes of the targeted behavior. BioMed Central 2019-09-18 /pmc/articles/PMC6751877/ /pubmed/31548864 http://dx.doi.org/10.1186/s13036-019-0205-0 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Pušnik, žiga Mraz, Miha Zimic, Nikolaj Moškon, Miha Computational analysis of viable parameter regions in models of synthetic biological systems |
title | Computational analysis of viable parameter regions in models of synthetic biological systems |
title_full | Computational analysis of viable parameter regions in models of synthetic biological systems |
title_fullStr | Computational analysis of viable parameter regions in models of synthetic biological systems |
title_full_unstemmed | Computational analysis of viable parameter regions in models of synthetic biological systems |
title_short | Computational analysis of viable parameter regions in models of synthetic biological systems |
title_sort | computational analysis of viable parameter regions in models of synthetic biological systems |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751877/ https://www.ncbi.nlm.nih.gov/pubmed/31548864 http://dx.doi.org/10.1186/s13036-019-0205-0 |
work_keys_str_mv | AT pusnikziga computationalanalysisofviableparameterregionsinmodelsofsyntheticbiologicalsystems AT mrazmiha computationalanalysisofviableparameterregionsinmodelsofsyntheticbiologicalsystems AT zimicnikolaj computationalanalysisofviableparameterregionsinmodelsofsyntheticbiologicalsystems AT moskonmiha computationalanalysisofviableparameterregionsinmodelsofsyntheticbiologicalsystems |