Complex Sciences. First International Conference, Complex 2009, Shanghai, China, February 23-25, 2009. Revised Papers, Part 1

Research Article

Modeling a Complex Biological Network with Temporal Heterogeneity: Cardiac Myocyte Plasticity as a Case Study

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  • @INPROCEEDINGS{10.1007/978-3-642-02466-5_46,
        author={Amin Mazloom and Kalyan Basu and Subhrangsu Mandal and Sajal Das},
        title={Modeling a Complex Biological Network with Temporal Heterogeneity: Cardiac Myocyte Plasticity as a Case Study},
        proceedings={Complex Sciences. First International Conference, Complex 2009, Shanghai, China, February 23-25, 2009. Revised Papers, Part 1},
        proceedings_a={COMPLEX PART 1},
        year={2012},
        month={5},
        keywords={},
        doi={10.1007/978-3-642-02466-5_46}
    }
    
  • Amin Mazloom
    Kalyan Basu
    Subhrangsu Mandal
    Sajal Das
    Year: 2012
    Modeling a Complex Biological Network with Temporal Heterogeneity: Cardiac Myocyte Plasticity as a Case Study
    COMPLEX PART 1
    Springer
    DOI: 10.1007/978-3-642-02466-5_46
Amin Mazloom1,*, Kalyan Basu2, Subhrangsu Mandal3, Sajal Das2
  • 1: Department of Pharmacology & Systems Therapeutics Mount Sinai School of Medicine
  • 2: Department of Computer Science & Engineering
  • 3: University of Texas at Arlington
*Contact email: amin.mazloom@mssm.edu

Abstract

Complex biological systems often characterize nonlinear dynamics. Employing traditional deterministic or stochastic approaches to quantify these dynamics either fail to capture their existing deviant effects or lead to combinatorial explosion. In this work we devised a novel approach that projects the biological functions within a pathway to a network of stochastic events that are random in time and space. By applying this approach recursively to the object system we build the event network of the entire system. The dynamics of the system evolves through the execution of the event network by a simulation engine which comprised of a time prioritized event queue. As a case study we utilized the current method and conducted an in-silico experiment on the metabolic plasticity of a cardiac myocyete. We aimed to quantify the down stream effects of insulin signaling that predominantly controls the plasticity in myocardium. Intriguingly, our in-silico results on transcription regulatory effect of insulin showed a good agreement with experimental data. Meanwhile we were able to characterize the flux change across major metabolic pathways over 48 hours of the in-silico experiment. Our simulation performed a remarkable efficiency by conducting 48 hours of simulation-time in less that 2 hours of processor time.