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Community guidelines for GPCR ligand bias: IUPHAR review 32
GPCRs modulate a plethora of physiological processes and mediate the effects of one‐third of FDA‐approved drugs. Depending on which ligand activates a receptor, it can engage different intracellular transducers. This ‘biased signalling’ paradigm requires that we now characterize physiological signal...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612872/ https://www.ncbi.nlm.nih.gov/pubmed/35106752 http://dx.doi.org/10.1111/bph.15811 |
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author | Kolb, Peter Kenakin, Terry Alexander, Stephen P. H. Bermudez, Marcel Bohn, Laura M. Breinholt, Christian S. Bouvier, Michel Hill, Stephen J. Kostenis, Evi Martemyanov, Kirill A. Neubig, Rick R. Onaran, H. Ongun Rajagopal, Sudarshan Roth, Bryan L. Selent, Jana Shukla, Arun K. Sommer, Martha E. Gloriam, David E. |
author_facet | Kolb, Peter Kenakin, Terry Alexander, Stephen P. H. Bermudez, Marcel Bohn, Laura M. Breinholt, Christian S. Bouvier, Michel Hill, Stephen J. Kostenis, Evi Martemyanov, Kirill A. Neubig, Rick R. Onaran, H. Ongun Rajagopal, Sudarshan Roth, Bryan L. Selent, Jana Shukla, Arun K. Sommer, Martha E. Gloriam, David E. |
author_sort | Kolb, Peter |
collection | PubMed |
description | GPCRs modulate a plethora of physiological processes and mediate the effects of one‐third of FDA‐approved drugs. Depending on which ligand activates a receptor, it can engage different intracellular transducers. This ‘biased signalling’ paradigm requires that we now characterize physiological signalling not just by receptors but by ligand–receptor pairs. Ligands eliciting biased signalling may constitute better drugs with higher efficacy and fewer adverse effects. However, ligand bias is very complex, making reproducibility and description challenging. Here, we provide guidelines and terminology for any scientists to design and report ligand bias experiments. The guidelines will aid consistency and clarity, as the basic receptor research and drug discovery communities continue to advance our understanding and exploitation of ligand bias. Scientific insight, biosensors, and analytical methods are still evolving and should benefit from and contribute to the implementation of the guidelines, together improving translation from in vitro to disease‐relevant in vivo models. |
format | Online Article Text |
id | pubmed-7612872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76128722022-07-01 Community guidelines for GPCR ligand bias: IUPHAR review 32 Kolb, Peter Kenakin, Terry Alexander, Stephen P. H. Bermudez, Marcel Bohn, Laura M. Breinholt, Christian S. Bouvier, Michel Hill, Stephen J. Kostenis, Evi Martemyanov, Kirill A. Neubig, Rick R. Onaran, H. Ongun Rajagopal, Sudarshan Roth, Bryan L. Selent, Jana Shukla, Arun K. Sommer, Martha E. Gloriam, David E. Br J Pharmacol Invited Review GPCRs modulate a plethora of physiological processes and mediate the effects of one‐third of FDA‐approved drugs. Depending on which ligand activates a receptor, it can engage different intracellular transducers. This ‘biased signalling’ paradigm requires that we now characterize physiological signalling not just by receptors but by ligand–receptor pairs. Ligands eliciting biased signalling may constitute better drugs with higher efficacy and fewer adverse effects. However, ligand bias is very complex, making reproducibility and description challenging. Here, we provide guidelines and terminology for any scientists to design and report ligand bias experiments. The guidelines will aid consistency and clarity, as the basic receptor research and drug discovery communities continue to advance our understanding and exploitation of ligand bias. Scientific insight, biosensors, and analytical methods are still evolving and should benefit from and contribute to the implementation of the guidelines, together improving translation from in vitro to disease‐relevant in vivo models. John Wiley and Sons Inc. 2022-03-27 2022-07 /pmc/articles/PMC7612872/ /pubmed/35106752 http://dx.doi.org/10.1111/bph.15811 Text en © 2022 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Review Kolb, Peter Kenakin, Terry Alexander, Stephen P. H. Bermudez, Marcel Bohn, Laura M. Breinholt, Christian S. Bouvier, Michel Hill, Stephen J. Kostenis, Evi Martemyanov, Kirill A. Neubig, Rick R. Onaran, H. Ongun Rajagopal, Sudarshan Roth, Bryan L. Selent, Jana Shukla, Arun K. Sommer, Martha E. Gloriam, David E. Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title | Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title_full | Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title_fullStr | Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title_full_unstemmed | Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title_short | Community guidelines for GPCR ligand bias: IUPHAR review 32 |
title_sort | community guidelines for gpcr ligand bias: iuphar review 32 |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612872/ https://www.ncbi.nlm.nih.gov/pubmed/35106752 http://dx.doi.org/10.1111/bph.15811 |
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