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AJP - Endocrinology and Metabolism, Vol 266, Issue 3 E341-E350, Copyright © 1994 by American Physiological Society
ARTICLES |
D. M. Cohen and R. N. Bergman
Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
We propose a syntactic approach to modeling of biochemical fluxes that combines a rule-based description of atomic transfer in chemical reactions with a structurally oriented, stochastic model of chemical reaction kinetics. This approach avoids the use of differential equations to describe the production and disappearance of each molecule. The computer simulation predicts the changes over time in the abundance of each positional isotopomer of every metabolic intermediate in the citric acid cycle of heart cells, subsequent to administration of [2-13C]acetate (including natural abundance of 13C). (Positional isotopomers are isomers that differ in the positions of isotopes within the molecule.) The 32 positional isotopomers of glutamate fell into four groups with similar intragroup dynamics but with very different amplitudes. From the relative abundance of each isotopomer of glutamate, we calculate the relative area of multiplets of the nuclear magnetic resonance spectrum.
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B. Comte, G. Vincent, B. Bouchard, and C. D. Rosiers Probing the Origin of Acetyl-CoA and Oxaloacetate Entering the Citric Acid Cycle from the 13C Labeling of Citrate Released by Perfused Rat Hearts J. Biol. Chem., October 17, 1997; 272(42): 26117 - 26124. [Abstract] [Full Text] [PDF] |
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