Multi-Target Analysis and Design of Mitochondrial Metabolism

Claudio Angione, Jole Costanza, Giovanni Carapezza, Pietro Lió, Giuseppe Nicosia

    Research output: Contribution to journalArticlepeer-review

    131 Downloads (Pure)


    Analyzing and optimizing biological models is often identified as a research priority in biomedical engineering. An important feature of a model should be the ability to find the best condition in which an organism has to be grown in order to reach specific optimal output values chosen by the researcher. In this work, we take into account a mitochondrial model analyzed with flux-balance analysis. The optimal design and assessment of these models is achieved through single- and/or multi-objective optimization techniques driven by epsilon-dominance and identifiability analysis. Our optimization algorithm searches for the values of the flux rates that optimize multiple cellular functions simultaneously. The optimization of the fluxes of the metabolic network includes not only input fluxes, but also internal fluxes. A faster convergence process with robust candidate solutions is permitted by a relaxed Pareto dominance, regulating the granularity of the approximation of the desired Pareto front. We find that the maximum ATP production is linked to a total consumption of NADH, and reaching the maximum amount of NADH leads to an increasing request of NADH from the external environment. Furthermore, the identifiability analysis characterizes the type and the stage of three monogenic diseases. Finally, we propose a new methodology to extend any constraint-based model using protein abundances.
    Original languageEnglish
    Pages (from-to)-
    JournalPLoS ONE
    Publication statusPublished - 16 Sept 2015


    Dive into the research topics of 'Multi-Target Analysis and Design of Mitochondrial Metabolism'. Together they form a unique fingerprint.

    Cite this