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Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor

We describe a label-free integrative pharmacology on-target (iPOT) method to assess the pharmacology of drugs at the β(2)-adrenergic receptor. This method combines dynamic mass redistribution (DMR) assays using an array of probe molecule-hijacked cells with similarity analysis. The whole cell DMR as...

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Autores principales: Ferrie, Ann M., Sun, Haiyan, Fang, Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216520/
https://www.ncbi.nlm.nih.gov/pubmed/22355552
http://dx.doi.org/10.1038/srep00033
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author Ferrie, Ann M.
Sun, Haiyan
Fang, Ye
author_facet Ferrie, Ann M.
Sun, Haiyan
Fang, Ye
author_sort Ferrie, Ann M.
collection PubMed
description We describe a label-free integrative pharmacology on-target (iPOT) method to assess the pharmacology of drugs at the β(2)-adrenergic receptor. This method combines dynamic mass redistribution (DMR) assays using an array of probe molecule-hijacked cells with similarity analysis. The whole cell DMR assays track cell system-based, ligand-directed, and kinetics-dependent biased activities of the drugs, and translates their on-target pharmacology into numerical descriptors which are subject to similarity analysis. We demonstrate that the approach establishes an effective link between the label-free pharmacology and in vivo therapeutic indications of drugs.
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spelling pubmed-32165202011-12-22 Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor Ferrie, Ann M. Sun, Haiyan Fang, Ye Sci Rep Article We describe a label-free integrative pharmacology on-target (iPOT) method to assess the pharmacology of drugs at the β(2)-adrenergic receptor. This method combines dynamic mass redistribution (DMR) assays using an array of probe molecule-hijacked cells with similarity analysis. The whole cell DMR assays track cell system-based, ligand-directed, and kinetics-dependent biased activities of the drugs, and translates their on-target pharmacology into numerical descriptors which are subject to similarity analysis. We demonstrate that the approach establishes an effective link between the label-free pharmacology and in vivo therapeutic indications of drugs. Nature Publishing Group 2011-07-07 /pmc/articles/PMC3216520/ /pubmed/22355552 http://dx.doi.org/10.1038/srep00033 Text en Copyright © 2011, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Ferrie, Ann M.
Sun, Haiyan
Fang, Ye
Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title_full Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title_fullStr Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title_full_unstemmed Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title_short Label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
title_sort label-free integrative pharmacology on-target of drugs at the β(2)-adrenergic receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3216520/
https://www.ncbi.nlm.nih.gov/pubmed/22355552
http://dx.doi.org/10.1038/srep00033
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