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Biochemical Systems Theory





REPRESENTATION

The dynamics of a specie is represented by a differential equation with the structure:

rac{dX_i}{dt}=\sum_j \sigma_{ij} \cdot \gamma_j \prod_k X_k^{g_{jk}}\,


where Xi represents one of the nd variables of the model (metabolite concentrations, protein concentrations or levels of gene expression). j represents the nf biochemical processes affecting the dynamics of the specie. On the other hand, \sigmaij (stoichiometric coefficient), \gammaj (rate constants) and gik (kinetic orders) are two different kinds of parameters defining the dynamics of the system.

The principal difference of Power-law Model s with respect to other ODE models used in biochemical systems is that the kinetic orders can be non-integer numbers. A kinetic order can have even negative value when inhibition is modelled. In this way, power-law models have a higher flexibility to reproduce the non-linearity of biochemical systems.

Models using power-law expansions have been used during the last 35 years to model and analyse several kinds of biochemical systems including metabolic networks, genetic networks and recently in cell signalling.


LITERATURE

Books:
  • M.A. Savageau, ''Biochemical systems analysis: a study of function and design in molecular biology'', Reading, MA, Addison–Wesley, 1976.

  • E.O. Voit (ed), ''Canonical Nonlinear Modeling. S-System Approach to Understanding Complexity'', Van Nostrand Reinhold, NY, 1991.

  • E.O. Voit, ''Computational Analysis of Biochemical Systems. A Practical Guide for Biochemists and Molecular Biologists'', Cambridge University Press, Cambridge, U.K., 2000.

  • N.V. Torres and E.O. Voit, ''Pathway Analysis and Optimization in Metabolic Engineering'', Cambridge University Press, Cambridge, U.K., 2002.


Scientific articles:
  • M.A. Savageau, ''Biochemical systems analysis: I. Some mathematical properties of the rate law for the component enzymatic reactions'' in: J. Theor. Biol. 25, pp. 365-369, 1969.

  • M.A. Savageau, ''Development of fractal kinetic theory for enzyme-catalysed reactions and implications for the design of biochemical pathways'' in: Biosystems 47(1-2), pp. 9-36, 1998.

  • M.R. Atkinson et al, ''Design of gene circuits using power-law models'', in: Cell 113, pp. 597–607, 2003.

  • F. Alvarez-Vasquez et al, ''Simulation and validation of modelled sphingolipid metabolism in Saccharomyces cerevisiae'', Nature 27, pp. 433(7024), pp. 425-30, 2005.

  • J. Vera et al, ''Power-Law models of signal transduction pathways'' in: Cellular Signalling doi:10.1016/j.cellsig.2007.01.029), 2007.

  • Eberhart O. Voit, ''Applications of Biochemical Systems Theory'' , 2006.



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