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Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches
Metabolic pathway modeling plays an increasing role in drug design by allowing better understanding of the underlying regulation and controlling networks in the metabolism of living organisms. However, despite rapid progress in this area, pathway modeling can become a real nightmare for researchers,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417601/ https://www.ncbi.nlm.nih.gov/pubmed/32778715 http://dx.doi.org/10.1038/s41598-020-70295-5 |
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author | Lo-Thong, Ophélie Charton, Philippe Cadet, Xavier F. Grondin-Perez, Brigitte Saavedra, Emma Damour, Cédric Cadet, Frédéric |
author_facet | Lo-Thong, Ophélie Charton, Philippe Cadet, Xavier F. Grondin-Perez, Brigitte Saavedra, Emma Damour, Cédric Cadet, Frédéric |
author_sort | Lo-Thong, Ophélie |
collection | PubMed |
description | Metabolic pathway modeling plays an increasing role in drug design by allowing better understanding of the underlying regulation and controlling networks in the metabolism of living organisms. However, despite rapid progress in this area, pathway modeling can become a real nightmare for researchers, notably when few experimental data are available or when the pathway is highly complex. Here, three different approaches were developed to model the second part of glycolysis of E. histolytica as an application example, and have succeeded in predicting the final pathway flux: one including detailed kinetic information (white-box), another with an added adjustment term (grey-box) and the last one using an artificial neural network method (black-box). Afterwards, each model was used for metabolic control analysis and flux control coefficient determination. The first two enzymes of this pathway are identified as the key enzymes playing a role in flux control. This study revealed the significance of the three methods for building suitable models adjusted to the available data in the field of metabolic pathway modeling, and could be useful to biologists and modelers. |
format | Online Article Text |
id | pubmed-7417601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74176012020-08-11 Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches Lo-Thong, Ophélie Charton, Philippe Cadet, Xavier F. Grondin-Perez, Brigitte Saavedra, Emma Damour, Cédric Cadet, Frédéric Sci Rep Article Metabolic pathway modeling plays an increasing role in drug design by allowing better understanding of the underlying regulation and controlling networks in the metabolism of living organisms. However, despite rapid progress in this area, pathway modeling can become a real nightmare for researchers, notably when few experimental data are available or when the pathway is highly complex. Here, three different approaches were developed to model the second part of glycolysis of E. histolytica as an application example, and have succeeded in predicting the final pathway flux: one including detailed kinetic information (white-box), another with an added adjustment term (grey-box) and the last one using an artificial neural network method (black-box). Afterwards, each model was used for metabolic control analysis and flux control coefficient determination. The first two enzymes of this pathway are identified as the key enzymes playing a role in flux control. This study revealed the significance of the three methods for building suitable models adjusted to the available data in the field of metabolic pathway modeling, and could be useful to biologists and modelers. Nature Publishing Group UK 2020-08-10 /pmc/articles/PMC7417601/ /pubmed/32778715 http://dx.doi.org/10.1038/s41598-020-70295-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lo-Thong, Ophélie Charton, Philippe Cadet, Xavier F. Grondin-Perez, Brigitte Saavedra, Emma Damour, Cédric Cadet, Frédéric Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title_full | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title_fullStr | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title_full_unstemmed | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title_short | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
title_sort | identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417601/ https://www.ncbi.nlm.nih.gov/pubmed/32778715 http://dx.doi.org/10.1038/s41598-020-70295-5 |
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