Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Beard, Daniel A
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1201326/
https://www.ncbi.nlm.nih.gov/pubmed/16163394
http://dx.doi.org/10.1371/journal.pcbi.0010036
_version_ 1782124901941903360
author Beard, Daniel A
author_facet Beard, Daniel A
author_sort Beard, Daniel A
collection PubMed
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.
format Text
id pubmed-1201326
institution National Center for Biotechnology Information
language English
publishDate 2005
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-12013262005-10-03 A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation Beard, Daniel A PLoS Comput Biol Research Article 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. Public Library of Science 2005-09 2005-09-09 /pmc/articles/PMC1201326/ /pubmed/16163394 http://dx.doi.org/10.1371/journal.pcbi.0010036 Text en Copyright: © 2005 Beard. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Beard, Daniel A
A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation
title 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_short A Biophysical Model of the Mitochondrial Respiratory System and Oxidative Phosphorylation
title_sort biophysical model of the mitochondrial respiratory system and oxidative phosphorylation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1201326/
https://www.ncbi.nlm.nih.gov/pubmed/16163394
http://dx.doi.org/10.1371/journal.pcbi.0010036
work_keys_str_mv AT bearddaniela abiophysicalmodelofthemitochondrialrespiratorysystemandoxidativephosphorylation
AT bearddaniela biophysicalmodelofthemitochondrialrespiratorysystemandoxidativephosphorylation