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Development of a chemogenomics library for phenotypic screening

With the development of advanced technologies in cell-based phenotypic screening, phenotypic drug discovery (PDD) strategies have re-emerged as promising approaches in the identification and development of novel and safe drugs. However, phenotypic screening does not rely on knowledge of specific dru...

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Autores principales: Dafniet, Bryan, Cerisier, Natacha, Boezio, Batiste, Clary, Anaelle, Ducrot, Pierre, Dorval, Thierry, Gohier, Arnaud, Brown, David, Audouze, Karine, Taboureau, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611952/
https://www.ncbi.nlm.nih.gov/pubmed/34819133
http://dx.doi.org/10.1186/s13321-021-00569-1
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author Dafniet, Bryan
Cerisier, Natacha
Boezio, Batiste
Clary, Anaelle
Ducrot, Pierre
Dorval, Thierry
Gohier, Arnaud
Brown, David
Audouze, Karine
Taboureau, Olivier
author_facet Dafniet, Bryan
Cerisier, Natacha
Boezio, Batiste
Clary, Anaelle
Ducrot, Pierre
Dorval, Thierry
Gohier, Arnaud
Brown, David
Audouze, Karine
Taboureau, Olivier
author_sort Dafniet, Bryan
collection PubMed
description With the development of advanced technologies in cell-based phenotypic screening, phenotypic drug discovery (PDD) strategies have re-emerged as promising approaches in the identification and development of novel and safe drugs. However, phenotypic screening does not rely on knowledge of specific drug targets and needs to be combined with chemical biology approaches to identify therapeutic targets and mechanisms of actions induced by drugs and associated with an observable phenotype. In this study, we developed a system pharmacology network integrating drug-target-pathway-disease relationships as well as morphological profile from an existing high content imaging-based high-throughput phenotypic profiling assay known as “Cell Painting”. Furthermore, from this network, a chemogenomic library of 5000 small molecules that represent a large and diverse panel of drug targets involved in diverse biological effects and diseases has been developed. Such a platform and a chemogenomic library could assist in the target identification and mechanism deconvolution of some phenotypic assays. The usefulness of the platform is illustrated through examples. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-021-00569-1.
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spelling pubmed-86119522021-11-29 Development of a chemogenomics library for phenotypic screening Dafniet, Bryan Cerisier, Natacha Boezio, Batiste Clary, Anaelle Ducrot, Pierre Dorval, Thierry Gohier, Arnaud Brown, David Audouze, Karine Taboureau, Olivier J Cheminform Research Article With the development of advanced technologies in cell-based phenotypic screening, phenotypic drug discovery (PDD) strategies have re-emerged as promising approaches in the identification and development of novel and safe drugs. However, phenotypic screening does not rely on knowledge of specific drug targets and needs to be combined with chemical biology approaches to identify therapeutic targets and mechanisms of actions induced by drugs and associated with an observable phenotype. In this study, we developed a system pharmacology network integrating drug-target-pathway-disease relationships as well as morphological profile from an existing high content imaging-based high-throughput phenotypic profiling assay known as “Cell Painting”. Furthermore, from this network, a chemogenomic library of 5000 small molecules that represent a large and diverse panel of drug targets involved in diverse biological effects and diseases has been developed. Such a platform and a chemogenomic library could assist in the target identification and mechanism deconvolution of some phenotypic assays. The usefulness of the platform is illustrated through examples. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-021-00569-1. Springer International Publishing 2021-11-24 /pmc/articles/PMC8611952/ /pubmed/34819133 http://dx.doi.org/10.1186/s13321-021-00569-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Dafniet, Bryan
Cerisier, Natacha
Boezio, Batiste
Clary, Anaelle
Ducrot, Pierre
Dorval, Thierry
Gohier, Arnaud
Brown, David
Audouze, Karine
Taboureau, Olivier
Development of a chemogenomics library for phenotypic screening
title Development of a chemogenomics library for phenotypic screening
title_full Development of a chemogenomics library for phenotypic screening
title_fullStr Development of a chemogenomics library for phenotypic screening
title_full_unstemmed Development of a chemogenomics library for phenotypic screening
title_short Development of a chemogenomics library for phenotypic screening
title_sort development of a chemogenomics library for phenotypic screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611952/
https://www.ncbi.nlm.nih.gov/pubmed/34819133
http://dx.doi.org/10.1186/s13321-021-00569-1
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