ArticleBMC systems biology2010
Modelling biochemical networks with intrinsic time delays: a hybrid semi-parametric approach.
Article in BMC systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- Impact of Influenza A Virus Infection on Growth and Metabolism of Suspension MDCK Cells Using a Dynamic Model.Metabolites · 2022Article
- Development of a hybrid model for a partially known intracellular signaling pathway through correction term estimation and neural network modeling.PLoS computational biology · 2020Article
- Towards a widespread adoption of metabolic modeling tools in biopharmaceutical industry: a process systems biology engineering perspective.NPJ systems biology and applications · 2020Review
- Hybrid semiparametric systems for quantitative sequence-activity modeling of synthetic biological parts.Synthetic biology (Oxford, England) · 2018Article
- Multi-level and hybrid modelling approaches for systems biology.Computational and structural biotechnology journal · 2017Review
- Refining ensembles of predicted gene regulatory networks based on characteristic interaction sets.PloS one · 2014Article
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Authors and funding
4 authors.
Funding
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Abstract
backgroundThis 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.
resultsThe 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.
conclusionsSignificantly 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.
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