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A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins

The present protocol describes a method by which interactions between G protein-coupled receptors (GPCR) and intracellular proteins can be monitored in real-time and without the use of exogenous labels. The method is based on surface plasmon resonance (SPR) and uses synthetic peptides as mimics of i...

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Autor principal: Stroth, Nikolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: jbm 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706161/
https://www.ncbi.nlm.nih.gov/pubmed/31453205
http://dx.doi.org/10.14440/jbm.2016.97
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author Stroth, Nikolas
author_facet Stroth, Nikolas
author_sort Stroth, Nikolas
collection PubMed
description The present protocol describes a method by which interactions between G protein-coupled receptors (GPCR) and intracellular proteins can be monitored in real-time and without the use of exogenous labels. The method is based on surface plasmon resonance (SPR) and uses synthetic peptides as mimics of intracellular GPCR domains. These peptides are covalently immobilized onto sensor chips and brought into contact with putative interacting proteins in the flow cells of the SPR instrument. The method allows flexible experimental designs, rapid testing of hypotheses and quantitative analysis of interactions. Relative to other established methods, it provides both an alternative and a complementary approach with several key advantages. The present protocol describes the method step-by-step, using the interaction between the serotonin 5-HT(7) receptor and the calcium-binding protein S100B as an example.
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spelling pubmed-67061612019-08-26 A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins Stroth, Nikolas J Biol Methods Protocol The present protocol describes a method by which interactions between G protein-coupled receptors (GPCR) and intracellular proteins can be monitored in real-time and without the use of exogenous labels. The method is based on surface plasmon resonance (SPR) and uses synthetic peptides as mimics of intracellular GPCR domains. These peptides are covalently immobilized onto sensor chips and brought into contact with putative interacting proteins in the flow cells of the SPR instrument. The method allows flexible experimental designs, rapid testing of hypotheses and quantitative analysis of interactions. Relative to other established methods, it provides both an alternative and a complementary approach with several key advantages. The present protocol describes the method step-by-step, using the interaction between the serotonin 5-HT(7) receptor and the calcium-binding protein S100B as an example. jbm 2016-01-28 /pmc/articles/PMC6706161/ /pubmed/31453205 http://dx.doi.org/10.14440/jbm.2016.97 Text en This work is licensed under a Creative Commons Attribution 3.0 License (http://creativecommons.org/licenses/by/3.0) .
spellingShingle Protocol
Stroth, Nikolas
A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title_full A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title_fullStr A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title_full_unstemmed A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title_short A surface plasmon resonance-based method for monitoring interactions between G protein-coupled receptors and interacting proteins
title_sort surface plasmon resonance-based method for monitoring interactions between g protein-coupled receptors and interacting proteins
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706161/
https://www.ncbi.nlm.nih.gov/pubmed/31453205
http://dx.doi.org/10.14440/jbm.2016.97
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