ArticleFrontiers in cell and developmental biology2016
Customized Steady-State Constraints for Parameter Estimation in Non-Linear Ordinary Differential Equation Models.
Article in Frontiers in cell and developmental biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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14 citing papers in PubMed.
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- Efficient computation of adjoint sensitivities at steady-state in ODE models of biochemical reaction networks.PLoS computational biology · 2023Article
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- Dynamic modeling of Nrf2 pathway activation in liver cells after toxicant exposure.Scientific reports · 2022Article
- Parameterization of mechanistic models from qualitative data using an efficient optimal scaling approach.Journal of mathematical biology · 2020Article
- Disentangling molecular mechanisms regulating sensitization of interferon alpha signal transduction.Molecular systems biology · 2020Article
- Benchmark problems for dynamic modeling of intracellular processes.Bioinformatics (Oxford, England) · 2019Article
- Benchmarking optimization methods for parameter estimation in large kinetic models.Bioinformatics (Oxford, England) · 2019Article
- Continuous analogue to iterative optimization for PDE-constrained inverse problems.Inverse problems in science and engineering · 2019Article
- Fitting mathematical models of biochemical pathways to steady state perturbation response data without simulating perturbation experiments.Scientific reports · 2018Article
- Predicting ligand-dependent tumors from multi-dimensional signaling features.NPJ systems biology and applications · 2017Article
- Tailored parameter optimization methods for ordinary differential equation models with steady-state constraints.BMC systems biology · 2016Article
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Abstract
Ordinary differential equation models have become a wide-spread approach to analyze dynamical systems and understand underlying mechanisms. Model parameters are often unknown and have to be estimated from experimental data, e.g., by maximum-likelihood estimation. In particular, models of biological systems contain a large number of parameters. To reduce the dimensionality of the parameter space, steady-state information is incorporated in the parameter estimation process. For non-linear models, analytical steady-state calculation typically leads to higher-order polynomial equations for which no closed-form solutions can be obtained. This can be circumvented by solving the steady-state equations for kinetic parameters, which results in a linear equation system with comparatively simple solutions. At the same time multiplicity of steady-state solutions is avoided, which otherwise is problematic for optimization. When solved for kinetic parameters, however, steady-state constraints tend to become negative for particular model specifications, thus, generating new types of optimization problems. Here, we present an algorithm based on graph theory that derives non-negative, analytical steady-state expressions by stepwise removal of cyclic dependencies between dynamical variables. The algorithm avoids multiple steady-state solutions by construction. We show that our method is applicable to most common classes of biochemical reaction networks containing inhibition terms, mass-action and Hill-type kinetic equations. Comparing the performance of parameter estimation for different analytical and numerical methods of incorporating steady-state information, we show that our approach is especially well-tailored to guarantee a high success rate of optimization.
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