Development of a chemogenomics library for phenotypic screening

Abstract 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 spe...

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Autores principales: Bryan Dafniet, Natacha Cerisier, Batiste Boezio, Anaelle Clary, Pierre Ducrot, Thierry Dorval, Arnaud Gohier, David Brown, Karine Audouze, Olivier Taboureau
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Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/51da2bea68b642218bf227d50acee1a6
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spelling oai:doaj.org-article:51da2bea68b642218bf227d50acee1a62021-11-28T12:30:25ZDevelopment of a chemogenomics library for phenotypic screening10.1186/s13321-021-00569-11758-2946https://doaj.org/article/51da2bea68b642218bf227d50acee1a62021-11-01T00:00:00Zhttps://doi.org/10.1186/s13321-021-00569-1https://doaj.org/toc/1758-2946Abstract 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.Bryan DafnietNatacha CerisierBatiste BoezioAnaelle ClaryPierre DucrotThierry DorvalArnaud GohierDavid BrownKarine AudouzeOlivier TaboureauBMCarticlePhenotypic screeningPhenotypic drug discoveryChemical biologySystem pharmacology networkNetwork pharmacologyChemogenomicsInformation technologyT58.5-58.64ChemistryQD1-999ENJournal of Cheminformatics, Vol 13, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Phenotypic screening
Phenotypic drug discovery
Chemical biology
System pharmacology network
Network pharmacology
Chemogenomics
Information technology
T58.5-58.64
Chemistry
QD1-999
spellingShingle Phenotypic screening
Phenotypic drug discovery
Chemical biology
System pharmacology network
Network pharmacology
Chemogenomics
Information technology
T58.5-58.64
Chemistry
QD1-999
Bryan Dafniet
Natacha Cerisier
Batiste Boezio
Anaelle Clary
Pierre Ducrot
Thierry Dorval
Arnaud Gohier
David Brown
Karine Audouze
Olivier Taboureau
Development of a chemogenomics library for phenotypic screening
description Abstract 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.
format article
author Bryan Dafniet
Natacha Cerisier
Batiste Boezio
Anaelle Clary
Pierre Ducrot
Thierry Dorval
Arnaud Gohier
David Brown
Karine Audouze
Olivier Taboureau
author_facet Bryan Dafniet
Natacha Cerisier
Batiste Boezio
Anaelle Clary
Pierre Ducrot
Thierry Dorval
Arnaud Gohier
David Brown
Karine Audouze
Olivier Taboureau
author_sort Bryan Dafniet
title Development of a chemogenomics library for phenotypic screening
title_short 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_sort development of a chemogenomics library for phenotypic screening
publisher BMC
publishDate 2021
url https://doaj.org/article/51da2bea68b642218bf227d50acee1a6
work_keys_str_mv AT bryandafniet developmentofachemogenomicslibraryforphenotypicscreening
AT natachacerisier developmentofachemogenomicslibraryforphenotypicscreening
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AT thierrydorval developmentofachemogenomicslibraryforphenotypicscreening
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