A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation.
A computational model for the mitochondrial respiratory chain that appropriately balances mass, charge, and free energy transduction is introduced and analyzed based on a previously published set of data measured on isolated cardiac mitochondria. The basic components included in the model are the re...
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2005-09-01
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Series: | PLoS Computational Biology |
Online Access: | http://dx.doi.org/10.1371/journal.pcbi.0010036 |
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doaj-5f9560432ba44af0b4b99833cea8c5a62020-11-25T01:02:22ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582005-09-0114e36A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation.A computational model for the mitochondrial respiratory chain that appropriately balances mass, charge, and free energy transduction is introduced and analyzed based on a previously published set of data measured on isolated cardiac mitochondria. The basic components included in the model are the reactions at complexes I, III, and IV of the electron transport system, ATP synthesis at F(1)F(0) ATPase, substrate transporters including adenine nucleotide translocase and the phosphate-hydrogen co-transporter, and cation fluxes across the inner membrane including fluxes through the K/H antiporter and passive H and K permeation. Estimation of 16 adjustable parameter values is based on fitting model simulations to nine independent data curves. The identified model is further validated by comparison to additional datasets measured from mitochondria isolated from rat heart and liver and observed at low oxygen concentration. To obtain reasonable fits to the available data, it is necessary to incorporate inorganic-phosphate-dependent activation of the dehydrogenase activity and the electron transport system. Specifically, it is shown that a model incorporating phosphate-dependent activation of complex III is able to reasonably reproduce the observed data. The resulting validated and verified model provides a foundation for building larger and more complex systems models and investigating complex physiological and pathophysiological interactions in cardiac energetics.http://dx.doi.org/10.1371/journal.pcbi.0010036 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
title |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. |
spellingShingle |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. PLoS Computational Biology |
title_short |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. |
title_full |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. |
title_fullStr |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. |
title_full_unstemmed |
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation. |
title_sort |
biophysical model of the mitochondrial respiratory system and oxidative phosphorylation. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Computational Biology |
issn |
1553-734X 1553-7358 |
publishDate |
2005-09-01 |
description |
A computational model for the mitochondrial respiratory chain that appropriately balances mass, charge, and free energy transduction is introduced and analyzed based on a previously published set of data measured on isolated cardiac mitochondria. The basic components included in the model are the reactions at complexes I, III, and IV of the electron transport system, ATP synthesis at F(1)F(0) ATPase, substrate transporters including adenine nucleotide translocase and the phosphate-hydrogen co-transporter, and cation fluxes across the inner membrane including fluxes through the K/H antiporter and passive H and K permeation. Estimation of 16 adjustable parameter values is based on fitting model simulations to nine independent data curves. The identified model is further validated by comparison to additional datasets measured from mitochondria isolated from rat heart and liver and observed at low oxygen concentration. To obtain reasonable fits to the available data, it is necessary to incorporate inorganic-phosphate-dependent activation of the dehydrogenase activity and the electron transport system. Specifically, it is shown that a model incorporating phosphate-dependent activation of complex III is able to reasonably reproduce the observed data. The resulting validated and verified model provides a foundation for building larger and more complex systems models and investigating complex physiological and pathophysiological interactions in cardiac energetics. |
url |
http://dx.doi.org/10.1371/journal.pcbi.0010036 |
_version_ |
1725205237739814912 |