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Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach
BACKGROUND: This paper presents a method for modelling dynamical biochemical networks with intrinsic time delays. Since the fundamental mechanisms leading to such delays are many times unknown, non conventional modelling approaches become necessary. Herein, a hybrid semi-parametric identification me...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955604/ https://www.ncbi.nlm.nih.gov/pubmed/20863397 http://dx.doi.org/10.1186/1752-0509-4-131 |
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author | von Stosch, Moritz Peres, Joana de Azevedo, Sebastião Feyo Oliveira, Rui |
author_facet | von Stosch, Moritz Peres, Joana de Azevedo, Sebastião Feyo Oliveira, Rui |
author_sort | von Stosch, Moritz |
collection | PubMed |
description | BACKGROUND: This paper presents a method for modelling dynamical biochemical networks with intrinsic time delays. Since the fundamental mechanisms leading to such delays are many times unknown, non conventional modelling approaches become necessary. Herein, a hybrid semi-parametric identification methodology is proposed in which discrete time series are incorporated into fundamental material balance models. This integration results in hybrid delay differential equations which can be applied to identify unknown cellular dynamics. RESULTS: The proposed hybrid modelling methodology was evaluated using two case studies. The first of these deals with dynamic modelling of transcriptional factor A in mammalian cells. The protein transport from the cytosol to the nucleus introduced a delay that was accounted for by discrete time series formulation. The second case study focused on a simple network with distributed time delays that demonstrated that the discrete time delay formalism has broad applicability to both discrete and distributed delay problems. CONCLUSIONS: Significantly better prediction qualities of the novel hybrid model were obtained when compared to dynamical structures without time delays, being the more distinctive the more significant the underlying system delay is. The identification of the system delays by studies of different discrete modelling delays was enabled by the proposed structure. Further, it was shown that the hybrid discrete delay methodology is not limited to discrete delay systems. The proposed method is a powerful tool to identify time delays in ill-defined biochemical networks. |
format | Text |
id | pubmed-2955604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29556042010-10-18 Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach von Stosch, Moritz Peres, Joana de Azevedo, Sebastião Feyo Oliveira, Rui BMC Syst Biol Methodology Article BACKGROUND: This paper presents a method for modelling dynamical biochemical networks with intrinsic time delays. Since the fundamental mechanisms leading to such delays are many times unknown, non conventional modelling approaches become necessary. Herein, a hybrid semi-parametric identification methodology is proposed in which discrete time series are incorporated into fundamental material balance models. This integration results in hybrid delay differential equations which can be applied to identify unknown cellular dynamics. RESULTS: The proposed hybrid modelling methodology was evaluated using two case studies. The first of these deals with dynamic modelling of transcriptional factor A in mammalian cells. The protein transport from the cytosol to the nucleus introduced a delay that was accounted for by discrete time series formulation. The second case study focused on a simple network with distributed time delays that demonstrated that the discrete time delay formalism has broad applicability to both discrete and distributed delay problems. CONCLUSIONS: Significantly better prediction qualities of the novel hybrid model were obtained when compared to dynamical structures without time delays, being the more distinctive the more significant the underlying system delay is. The identification of the system delays by studies of different discrete modelling delays was enabled by the proposed structure. Further, it was shown that the hybrid discrete delay methodology is not limited to discrete delay systems. The proposed method is a powerful tool to identify time delays in ill-defined biochemical networks. BioMed Central 2010-09-23 /pmc/articles/PMC2955604/ /pubmed/20863397 http://dx.doi.org/10.1186/1752-0509-4-131 Text en Copyright ©2010 von Stosch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article von Stosch, Moritz Peres, Joana de Azevedo, Sebastião Feyo Oliveira, Rui Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title | Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title_full | Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title_fullStr | Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title_full_unstemmed | Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title_short | Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
title_sort | modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955604/ https://www.ncbi.nlm.nih.gov/pubmed/20863397 http://dx.doi.org/10.1186/1752-0509-4-131 |
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