Evidence map›Paper›PMID 24885656›Full record

ArticleBMC systems biology2014

A model reduction method for biochemical reaction networks.

Shodhan Rao, Arjan van der Schaft, Karen van Eunen, Barbara M Bakker, Bayu Jayawardhana

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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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23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shodhan Rao
Arjan van der Schaft
Karen van Eunen
Barbara M Bakker
Bayu JayawardhanaSystems Biology Center for Energy Metabolism and Ageing, University of Groningen, ERIBA, Antonius Deusinglaan 1 9713 AV Groningen, Netherlands. b.jayawardhana@rug.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Metabolic Networks and PathwaysModels, BiologicalAnimalsEnzymesFatty AcidsGlycolysisKineticsOxidation-ReductionRatsSaccharomyces cerevisiaeEnzymesFatty Acids

Identifiers

PMID24885656
PMCPMC4041147

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.