Cargando…

Label-free drug discovery

Current drug discovery is dominated by label-dependent molecular approaches, which screen drugs in the context of a predefined and target-based hypothesis in vitro. Given that target-based discovery has not transformed the industry, phenotypic screen that identifies drugs based on a specific phenoty...

Descripción completa

Detalles Bibliográficos
Autor principal: Fang, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973898/
https://www.ncbi.nlm.nih.gov/pubmed/24723889
http://dx.doi.org/10.3389/fphar.2014.00052
_version_ 1782479390386421760
author Fang, Ye
author_facet Fang, Ye
author_sort Fang, Ye
collection PubMed
description Current drug discovery is dominated by label-dependent molecular approaches, which screen drugs in the context of a predefined and target-based hypothesis in vitro. Given that target-based discovery has not transformed the industry, phenotypic screen that identifies drugs based on a specific phenotype of cells, tissues, or animals has gained renewed interest. However, owing to the intrinsic complexity in drug–target interactions, there is often a significant gap between the phenotype screened and the ultimate molecular mechanism of action sought. This paper presents a label-free strategy for early drug discovery. This strategy combines label-free cell phenotypic profiling with computational approaches, and holds promise to bridge the gap by offering a kinetic and holistic representation of the functional consequences of drugs in disease relevant cells that is amenable to mechanistic deconvolution.
format Online
Article
Text
id pubmed-3973898
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-39738982014-04-10 Label-free drug discovery Fang, Ye Front Pharmacol Pharmacology Current drug discovery is dominated by label-dependent molecular approaches, which screen drugs in the context of a predefined and target-based hypothesis in vitro. Given that target-based discovery has not transformed the industry, phenotypic screen that identifies drugs based on a specific phenotype of cells, tissues, or animals has gained renewed interest. However, owing to the intrinsic complexity in drug–target interactions, there is often a significant gap between the phenotype screened and the ultimate molecular mechanism of action sought. This paper presents a label-free strategy for early drug discovery. This strategy combines label-free cell phenotypic profiling with computational approaches, and holds promise to bridge the gap by offering a kinetic and holistic representation of the functional consequences of drugs in disease relevant cells that is amenable to mechanistic deconvolution. Frontiers Media S.A. 2014-03-27 /pmc/articles/PMC3973898/ /pubmed/24723889 http://dx.doi.org/10.3389/fphar.2014.00052 Text en Copyright © 2014 Fang. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Fang, Ye
Label-free drug discovery
title Label-free drug discovery
title_full Label-free drug discovery
title_fullStr Label-free drug discovery
title_full_unstemmed Label-free drug discovery
title_short Label-free drug discovery
title_sort label-free drug discovery
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973898/
https://www.ncbi.nlm.nih.gov/pubmed/24723889
http://dx.doi.org/10.3389/fphar.2014.00052
work_keys_str_mv AT fangye labelfreedrugdiscovery