Abstract

BackgroundFlux balance analysis (FBA) together with its extension, dynamic FBA, have proven instrumental for analyzing the robustness and dynamics of metabolic networks by employing only the stoichiometry of the included reactions coupled with adequately chosen objective function. In addition, under the assumption of minimization of metabolic adjustment, dynamic FBA has recently been employed to analyze the transition between metabolic states.ResultsHere, we propose a suite of novel methods for analyzing the dynamics of (internally perturbed) metabolic networks and for quantifying their robustness with limited knowledge of kinetic parameters. Following the biochemically meaningful premise that metabolite concentrations exhibit smooth temporal changes, the proposed methods rely on minimizing the significant fluctuations of metabolic profiles to predict the time-resolved metabolic state, characterized by both fluxes and concentrations. By conducting a comparative analysis with a kinetic model of the Calvin-Benson cycle and a model of plant carbohydrate metabolism, we demonstrate that the principle of regulatory on/off minimization coupled with dynamic FBA can accurately predict the changes in metabolic states.ConclusionsOur methods outperform the existing dynamic FBA-based modeling alternatives, and could help in revealing the mechanisms for maintaining robustness of dynamic processes in metabolic networks over time.

Highlights

  • Flux balance analysis (FBA) together with its extension, dynamic FBA, have proven instrumental for analyzing the robustness and dynamics of metabolic networks by employing only the stoichiometry of the included reactions coupled with adequately chosen objective function

  • Since the proposed methods build upon the dynamic FBA (DFBA) approaches, we provide a brief overview of the mathematical apparatus used in their formulation

  • In the present work, we proposed a new approach to analyze the dynamic adjustment of metabolic networks, called R-DFBA

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Summary

Introduction

Flux balance analysis (FBA) together with its extension, dynamic FBA, have proven instrumental for analyzing the robustness and dynamics of metabolic networks by employing only the stoichiometry of the included reactions coupled with adequately chosen objective function. Recent advances in metabolomics have provided a large amount of highly reproducible data [2,3,4], allowing reconstruction and analysis of genome-scale metabolic networks [5] These developments in metabolomics technologies have challenged computational systems biology with the need to accurately describe the dynamics of metabolic networks in order to glean the flux rates at different time points, representing the temporal flux (re) distribution, and the interdependent metabolic profiles, Metabolic flux analysis (MFA) has propelled the development of computational methods for analysis of metabolic networks [11,12]. The classical FBA ignores the possibility that perturbed metabolic networks may not immediately regulate towards the (assumed) optimal objective

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