ArticleBMC systems biology2014
A model reduction method for biochemical reaction networks.
Article in BMC systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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23 citing papers in PubMed.
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- Metabolic kinetic modeling provides insight into complex biological questions, but hurdles remain.Current opinion in biotechnology · 2019Review
- Computational Approaches in Theranostics: Mining and Predicting Cancer Data.Pharmaceutics · 2019Review
- Deciphering noise amplification and reduction in open chemical reaction networks.Journal of the Royal Society, Interface · 2018Article
- Evaluating model reduction under parameter uncertainty.BMC systems biology · 2018Article
- DMPy: a Python package for automated mathematical model construction of large-scale metabolic systems.BMC systems biology · 2018Article
- Methods of Model Reduction for Large-Scale Biological Systems: A Survey of Current Methods and Trends.Bulletin of mathematical biology · 2017Article
- Models of Models: A Translational Route for Cancer Treatment and Drug Development.Frontiers in oncology · 2017Article
- Graphical reduction of reaction networks by linear elimination of species.Journal of mathematical biology · 2017Article
- Model reduction for stochastic CaMKII reaction kinetics in synapses by graph-constrained correlation dynamics.Physical biology · 2015Article
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5 authors.
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Abstract
backgroundIn this paper we propose a model reduction method for biochemical reaction networks governed by a variety of reversible and irreversible enzyme kinetic rate laws, including reversible Michaelis-Menten and Hill kinetics. The method proceeds by a stepwise reduction in the number of complexes, defined as the left and right-hand sides of the reactions in the network. It is based on the Kron reduction of the weighted Laplacian matrix, which describes the graph structure of the complexes and reactions in the network. It does not rely on prior knowledge of the dynamic behaviour of the network and hence can be automated, as we demonstrate. The reduced network has fewer complexes, reactions, variables and parameters as compared to the original network, and yet the behaviour of a preselected set of significant metabolites in the reduced network resembles that of the original network. Moreover the reduced network largely retains the structure and kinetics of the original model.
resultsWe apply our method to a yeast glycolysis model and a rat liver fatty acid beta-oxidation model. When the number of state variables in the yeast model is reduced from 12 to 7, the difference between metabolite concentrations in the reduced and the full model, averaged over time and species, is only 8%. Likewise, when the number of state variables in the rat-liver beta-oxidation model is reduced from 42 to 29, the difference between the reduced model and the full model is 7.5%.
conclusionsThe method has improved our understanding of the dynamics of the two networks. We found that, contrary to the general disposition, the first few metabolites which were deleted from the network during our stepwise reduction approach, are not those with the shortest convergence times. It shows that our reduction approach performs differently from other approaches that are based on time-scale separation. The method can be used to facilitate fitting of the parameters or to embed a detailed model of interest in a more coarse-grained yet realistic environment.
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