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Ligand bias in receptor tyrosine kinase signaling

Ligand bias is the ability of ligands to differentially activate certain receptor signaling responses compared with others. It reflects differences in the responses of a receptor to specific ligands and has implications for the development of highly specific therapeutics. Whereas ligand bias has bee...

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Detalles Bibliográficos
Autores principales: Karl, Kelly, Paul, Michael D., Pasquale, Elena B., Hristova, Kalina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7939482/
https://www.ncbi.nlm.nih.gov/pubmed/33122191
http://dx.doi.org/10.1074/jbc.REV120.015190
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author Karl, Kelly
Paul, Michael D.
Pasquale, Elena B.
Hristova, Kalina
author_facet Karl, Kelly
Paul, Michael D.
Pasquale, Elena B.
Hristova, Kalina
author_sort Karl, Kelly
collection PubMed
description Ligand bias is the ability of ligands to differentially activate certain receptor signaling responses compared with others. It reflects differences in the responses of a receptor to specific ligands and has implications for the development of highly specific therapeutics. Whereas ligand bias has been studied primarily for G protein–coupled receptors (GPCRs), there are also reports of ligand bias for receptor tyrosine kinases (RTKs). However, the understanding of RTK ligand bias is lagging behind the knowledge of GPCR ligand bias. In this review, we highlight how protocols that were developed to study GPCR signaling can be used to identify and quantify RTK ligand bias. We also introduce an operational model that can provide insights into the biophysical basis of RTK activation and ligand bias. Finally, we discuss possible mechanisms underpinning RTK ligand bias. Thus, this review serves as a primer for researchers interested in investigating ligand bias in RTK signaling.
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spelling pubmed-79394822021-06-08 Ligand bias in receptor tyrosine kinase signaling Karl, Kelly Paul, Michael D. Pasquale, Elena B. Hristova, Kalina J Biol Chem JBC Reviews Ligand bias is the ability of ligands to differentially activate certain receptor signaling responses compared with others. It reflects differences in the responses of a receptor to specific ligands and has implications for the development of highly specific therapeutics. Whereas ligand bias has been studied primarily for G protein–coupled receptors (GPCRs), there are also reports of ligand bias for receptor tyrosine kinases (RTKs). However, the understanding of RTK ligand bias is lagging behind the knowledge of GPCR ligand bias. In this review, we highlight how protocols that were developed to study GPCR signaling can be used to identify and quantify RTK ligand bias. We also introduce an operational model that can provide insights into the biophysical basis of RTK activation and ligand bias. Finally, we discuss possible mechanisms underpinning RTK ligand bias. Thus, this review serves as a primer for researchers interested in investigating ligand bias in RTK signaling. American Society for Biochemistry and Molecular Biology 2021-01-13 /pmc/articles/PMC7939482/ /pubmed/33122191 http://dx.doi.org/10.1074/jbc.REV120.015190 Text en © 2020 © 2020 Karl et al. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle JBC Reviews
Karl, Kelly
Paul, Michael D.
Pasquale, Elena B.
Hristova, Kalina
Ligand bias in receptor tyrosine kinase signaling
title Ligand bias in receptor tyrosine kinase signaling
title_full Ligand bias in receptor tyrosine kinase signaling
title_fullStr Ligand bias in receptor tyrosine kinase signaling
title_full_unstemmed Ligand bias in receptor tyrosine kinase signaling
title_short Ligand bias in receptor tyrosine kinase signaling
title_sort ligand bias in receptor tyrosine kinase signaling
topic JBC Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7939482/
https://www.ncbi.nlm.nih.gov/pubmed/33122191
http://dx.doi.org/10.1074/jbc.REV120.015190
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