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Integrated computational model of the bioenergetics of isolated lung mitochondria

Integrated computational modeling provides a mechanistic and quantitative framework for describing lung mitochondrial bioenergetics. Thus, the objective of this study was to develop and validate a thermodynamically-constrained integrated computational model of the bioenergetics of isolated lung mito...

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Autores principales: Zhang, Xiao, Dash, Ranjan K., Jacobs, Elizabeth R., Camara, Amadou K. S., Clough, Anne V., Audi, Said H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995348/
https://www.ncbi.nlm.nih.gov/pubmed/29889855
http://dx.doi.org/10.1371/journal.pone.0197921
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author Zhang, Xiao
Dash, Ranjan K.
Jacobs, Elizabeth R.
Camara, Amadou K. S.
Clough, Anne V.
Audi, Said H.
author_facet Zhang, Xiao
Dash, Ranjan K.
Jacobs, Elizabeth R.
Camara, Amadou K. S.
Clough, Anne V.
Audi, Said H.
author_sort Zhang, Xiao
collection PubMed
description Integrated computational modeling provides a mechanistic and quantitative framework for describing lung mitochondrial bioenergetics. Thus, the objective of this study was to develop and validate a thermodynamically-constrained integrated computational model of the bioenergetics of isolated lung mitochondria. The model incorporates the major biochemical reactions and transport processes in lung mitochondria. A general framework was developed to model those biochemical reactions and transport processes. Intrinsic model parameters such as binding constants were estimated using previously published isolated enzymes and transporters kinetic data. Extrinsic model parameters such as maximal reaction and transport velocities were estimated by fitting the integrated bioenergetics model to published and new tricarboxylic acid cycle and respirometry data measured in isolated rat lung mitochondria. The integrated model was then validated by assessing its ability to predict experimental data not used for the estimation of the extrinsic model parameters. For example, the model was able to predict reasonably well the substrate and temperature dependency of mitochondrial oxygen consumption, kinetics of NADH redox status, and the kinetics of mitochondrial accumulation of the cationic dye rhodamine 123, driven by mitochondrial membrane potential, under different respiratory states. The latter required the coupling of the integrated bioenergetics model to a pharmacokinetic model for the mitochondrial uptake of rhodamine 123 from buffer. The integrated bioenergetics model provides a mechanistic and quantitative framework for 1) integrating experimental data from isolated lung mitochondria under diverse experimental conditions, and 2) assessing the impact of a change in one or more mitochondrial processes on overall lung mitochondrial bioenergetics. In addition, the model provides important insights into the bioenergetics and respiration of lung mitochondria and how they differ from those of mitochondria from other organs. To the best of our knowledge, this model is the first for the bioenergetics of isolated lung mitochondria.
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spelling pubmed-59953482018-06-21 Integrated computational model of the bioenergetics of isolated lung mitochondria Zhang, Xiao Dash, Ranjan K. Jacobs, Elizabeth R. Camara, Amadou K. S. Clough, Anne V. Audi, Said H. PLoS One Research Article Integrated computational modeling provides a mechanistic and quantitative framework for describing lung mitochondrial bioenergetics. Thus, the objective of this study was to develop and validate a thermodynamically-constrained integrated computational model of the bioenergetics of isolated lung mitochondria. The model incorporates the major biochemical reactions and transport processes in lung mitochondria. A general framework was developed to model those biochemical reactions and transport processes. Intrinsic model parameters such as binding constants were estimated using previously published isolated enzymes and transporters kinetic data. Extrinsic model parameters such as maximal reaction and transport velocities were estimated by fitting the integrated bioenergetics model to published and new tricarboxylic acid cycle and respirometry data measured in isolated rat lung mitochondria. The integrated model was then validated by assessing its ability to predict experimental data not used for the estimation of the extrinsic model parameters. For example, the model was able to predict reasonably well the substrate and temperature dependency of mitochondrial oxygen consumption, kinetics of NADH redox status, and the kinetics of mitochondrial accumulation of the cationic dye rhodamine 123, driven by mitochondrial membrane potential, under different respiratory states. The latter required the coupling of the integrated bioenergetics model to a pharmacokinetic model for the mitochondrial uptake of rhodamine 123 from buffer. The integrated bioenergetics model provides a mechanistic and quantitative framework for 1) integrating experimental data from isolated lung mitochondria under diverse experimental conditions, and 2) assessing the impact of a change in one or more mitochondrial processes on overall lung mitochondrial bioenergetics. In addition, the model provides important insights into the bioenergetics and respiration of lung mitochondria and how they differ from those of mitochondria from other organs. To the best of our knowledge, this model is the first for the bioenergetics of isolated lung mitochondria. Public Library of Science 2018-06-11 /pmc/articles/PMC5995348/ /pubmed/29889855 http://dx.doi.org/10.1371/journal.pone.0197921 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Zhang, Xiao
Dash, Ranjan K.
Jacobs, Elizabeth R.
Camara, Amadou K. S.
Clough, Anne V.
Audi, Said H.
Integrated computational model of the bioenergetics of isolated lung mitochondria
title Integrated computational model of the bioenergetics of isolated lung mitochondria
title_full Integrated computational model of the bioenergetics of isolated lung mitochondria
title_fullStr Integrated computational model of the bioenergetics of isolated lung mitochondria
title_full_unstemmed Integrated computational model of the bioenergetics of isolated lung mitochondria
title_short Integrated computational model of the bioenergetics of isolated lung mitochondria
title_sort integrated computational model of the bioenergetics of isolated lung mitochondria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995348/
https://www.ncbi.nlm.nih.gov/pubmed/29889855
http://dx.doi.org/10.1371/journal.pone.0197921
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