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Tools for GPCR drug discovery
G-protein-coupled receptors (GPCRs) mediate many important physiological functions and are considered as one of the most successful therapeutic targets for a broad spectrum of diseases. The design and implementation of high-throughput GPCR assays that allow the cost-effective screening of large comp...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312097/ https://www.ncbi.nlm.nih.gov/pubmed/22266728 http://dx.doi.org/10.1038/aps.2011.173 |
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author | Zhang, Ru Xie, Xin |
author_facet | Zhang, Ru Xie, Xin |
author_sort | Zhang, Ru |
collection | PubMed |
description | G-protein-coupled receptors (GPCRs) mediate many important physiological functions and are considered as one of the most successful therapeutic targets for a broad spectrum of diseases. The design and implementation of high-throughput GPCR assays that allow the cost-effective screening of large compound libraries to identify novel drug candidates are critical in early drug discovery. Early functional GPCR assays depend primarily on the measurement of G-protein-mediated 2nd messenger generation. Taking advantage of the continuously deepening understanding of GPCR signal transduction, many G-protein-independent pathways are utilized to detect the activity of GPCRs, and may provide additional information on functional selectivity of candidate compounds. With the combination of automated imaging systems and label-free detection systems, such assays are now suitable for high-throughput screening (HTS). In this review, we summarize the most widely used GPCR assays and recent advances in HTS technologies for GPCR drug discovery. |
format | Online Article Text |
id | pubmed-3312097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33120972012-03-26 Tools for GPCR drug discovery Zhang, Ru Xie, Xin Acta Pharmacol Sin Review G-protein-coupled receptors (GPCRs) mediate many important physiological functions and are considered as one of the most successful therapeutic targets for a broad spectrum of diseases. The design and implementation of high-throughput GPCR assays that allow the cost-effective screening of large compound libraries to identify novel drug candidates are critical in early drug discovery. Early functional GPCR assays depend primarily on the measurement of G-protein-mediated 2nd messenger generation. Taking advantage of the continuously deepening understanding of GPCR signal transduction, many G-protein-independent pathways are utilized to detect the activity of GPCRs, and may provide additional information on functional selectivity of candidate compounds. With the combination of automated imaging systems and label-free detection systems, such assays are now suitable for high-throughput screening (HTS). In this review, we summarize the most widely used GPCR assays and recent advances in HTS technologies for GPCR drug discovery. Nature Publishing Group 2012-03 2012-01-23 /pmc/articles/PMC3312097/ /pubmed/22266728 http://dx.doi.org/10.1038/aps.2011.173 Text en Copyright © 2012 CPS and SIMM http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Review Zhang, Ru Xie, Xin Tools for GPCR drug discovery |
title | Tools for GPCR drug discovery |
title_full | Tools for GPCR drug discovery |
title_fullStr | Tools for GPCR drug discovery |
title_full_unstemmed | Tools for GPCR drug discovery |
title_short | Tools for GPCR drug discovery |
title_sort | tools for gpcr drug discovery |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312097/ https://www.ncbi.nlm.nih.gov/pubmed/22266728 http://dx.doi.org/10.1038/aps.2011.173 |
work_keys_str_mv | AT zhangru toolsforgpcrdrugdiscovery AT xiexin toolsforgpcrdrugdiscovery |