ArticleBMC systems biology2012
Estimation of dynamic flux profiles from metabolic time series data.
Article in BMC systems biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed.
- Optimal control of agent-based models via surrogate modeling.PLoS computational biology · 2025Article
- Towards inferring absolute concentrations from relative abundance in time-course GC-MS metabolomics data.Molecular omics · 2023Article
- Dynamic Flux Balance Analysis to Evaluate the Strain Production Performance on Shikimic Acid Production inMetabolites · 2020Article
- LK-DFBA: a linear programming-based modeling strategy for capturing dynamics and metabolite-dependent regulation in metabolism.BMC bioinformatics · 2020Article
- Identification of microbiota dynamics using robust parameter estimation methods.Mathematical biosciences · 2017Article
- The best models of metabolism.Wiley interdisciplinary reviews. Systems biology and medicine · 2017Review
- Metabolic adjustment upon repetitive substrate perturbations using dynamicMicrobial cell factories · 2017Article
- Nonparametric dynamic modeling.Mathematical biosciences · 2017Article
- Perspective: On the importance of hydrodynamic interactions in the subcellular dynamics of macromolecules.The Journal of chemical physics · 2016Article
- Identification of Metabolic Pathway Systems.Frontiers in genetics · 2016Article
- Mathematical Modeling and Dynamic Simulation of Metabolic Reaction Systems Using Metabolome Time Series Data.Frontiers in molecular biosciences · 2016Review
- Dynamic estimation of specific fluxes in metabolic networks using non-linear dynamic optimization.BMC systems biology · 2014Article
- Derivative processes for modelling metabolic fluxes.Bioinformatics (Oxford, England) · 2014Article
- Mesoscopic modeling as a starting point for computational analyses of cystic fibrosis as a systemic disease.Biochimica et biophysica acta · 2014Article
- Characterizability of metabolic pathway systems from time series data.Mathematical biosciences · 2013Article
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Abstract
backgroundAdvances in modern high-throughput techniques of molecular biology have enabled top-down approaches for the estimation of parameter values in metabolic systems, based on time series data. Special among them is the recent method of dynamic flux estimation (DFE), which uses such data not only for parameter estimation but also for the identification of functional forms of the processes governing a metabolic system. DFE furthermore provides diagnostic tools for the evaluation of model validity and of the quality of a model fit beyond residual errors. Unfortunately, DFE works only when the data are more or less complete and the system contains as many independent fluxes as metabolites. These drawbacks may be ameliorated with other types of estimation and information. However, such supplementations incur their own limitations. In particular, assumptions must be made regarding the functional forms of some processes and detailed kinetic information must be available, in addition to the time series data.
resultsThe authors propose here a systematic approach that supplements DFE and overcomes some of its shortcomings. Like DFE, the approach is model-free and requires only minimal assumptions. If sufficient time series data are available, the approach allows the determination of a subset of fluxes that enables the subsequent applicability of DFE to the rest of the flux system. The authors demonstrate the procedure with three artificial pathway systems exhibiting distinct characteristics and with actual data of the trehalose pathway in Saccharomyces cerevisiae.
conclusionsThe results demonstrate that the proposed method successfully complements DFE under various situations and without a priori assumptions regarding the model representation. The proposed method also permits an examination of whether at all, to what degree, or within what range the available time series data can be validly represented in a particular functional format of a flux within a pathway system. Based on these results, further experiments may be designed to generate data points that genuinely add new information to the structure identification and parameter estimation tasks at hand.
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