A Kinetic Finite Volume Discretization of the Multidimensional PIDE Model for Gene Regulatory Networks.
Mihály A Vághy1, Irene Otero-Muras2, Manuel Pájaro3
1Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Práter u. 50/a, Budapest, 1083, Hungary. vaghy.mihaly.andras@itk.ppke.hu.
A new finite volume method for partial integro-differential equations (PIDEs) in gene regulatory networks is introduced. This approach simplifies analysis of protein distribution dynamics and equilibrium states.
Area of Science:
- Computational Biology
- Systems Biology
- Mathematical Biology
Background:
- Gene regulatory networks (GRNs) involve complex protein distribution dynamics.
- Partial integro-differential equations (PIDEs) are often used to model these dynamics.
- Analyzing the stability and equilibria of these models can be mathematically challenging.
Purpose of the Study:
- To propose a novel finite volume discretization scheme for PIDEs in GRNs.
- To enable qualitative analysis of protein distribution dynamics using established theories.
- To provide a computationally efficient method for determining stationary distributions.
Main Methods:
- Developed a finite volume discretization scheme for PIDEs.
- Represented the resulting ordinary differential equations (ODEs) as a compartmental kinetic system.
- Applied the theory of nonnegative and compartmental systems for analysis.
Main Results:
- The scheme allows for straightforward analysis of the existence, uniqueness, and stability of equilibria.
- Computation of stationary probability distributions is reduced to solving linear equations.
- Demonstrated the precision and accuracy of the method through computational examples.
Conclusions:
- The proposed finite volume scheme offers a robust framework for analyzing protein dynamics in GRNs.
- It bridges the gap between complex PIDE models and established theories of compartmental systems.
- The method provides accurate results and facilitates efficient computation of key system properties.
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