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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...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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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 |
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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 |