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BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues

The concept of oligomerization of G protein-coupled receptor (GPCR) opens new perspectives regarding physiological function regulation. The capacity of one GPCR to modify its binding and coupling properties by interacting with a second one can be at the origin of regulations unsuspected two decades...

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Autores principales: Cottet, Martin, Faklaris, Orestis, Maurel, Damien, Scholler, Pauline, Doumazane, Etienne, Trinquet, Eric, Pin, Jean-Philippe, Durroux, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401989/
https://www.ncbi.nlm.nih.gov/pubmed/22837753
http://dx.doi.org/10.3389/fendo.2012.00092
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author Cottet, Martin
Faklaris, Orestis
Maurel, Damien
Scholler, Pauline
Doumazane, Etienne
Trinquet, Eric
Pin, Jean-Philippe
Durroux, Thierry
author_facet Cottet, Martin
Faklaris, Orestis
Maurel, Damien
Scholler, Pauline
Doumazane, Etienne
Trinquet, Eric
Pin, Jean-Philippe
Durroux, Thierry
author_sort Cottet, Martin
collection PubMed
description The concept of oligomerization of G protein-coupled receptor (GPCR) opens new perspectives regarding physiological function regulation. The capacity of one GPCR to modify its binding and coupling properties by interacting with a second one can be at the origin of regulations unsuspected two decades ago. Although the concept is interesting, its validation at a physiological level is challenging and probably explains why receptor oligomerization is still controversial. Demonstrating direct interactions between two proteins is not trivial since few techniques present a spatial resolution allowing this precision. Resonance energy transfer (RET) strategies are actually the most convenient ones. During the last two decades, bioluminescent resonance energy transfer and time-resolved fluorescence resonance energy transfer (TR-FRET) have been widely used since they exhibit high signal-to-noise ratio. Most of the experiments based on GPCR labeling have been performed in cell lines and it has been shown that all GPCRs have the propensity to form homo- or hetero-oligomers. However, whether these data can be extrapolated to GPCRs expressed in native tissues and explain receptor functioning in real life, remains an open question. Native tissues impose different constraints since GPCR sequences cannot be modified. Recently, a fluorescent ligand-based GPCR labeling strategy combined to a TR-FRET approach has been successfully used to prove the existence of GPCR oligomerization in native tissues. Although the RET-based strategies are generally quite simple to implement, precautions have to be taken before concluding to the absence or the existence of specific interactions between receptors. For example, one should exclude the possibility of collision of receptors diffusing throughout the membrane leading to a specific FRET signal. The advantages and the limits of different approaches will be reviewed and the consequent perspectives discussed.
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spelling pubmed-34019892012-07-26 BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues Cottet, Martin Faklaris, Orestis Maurel, Damien Scholler, Pauline Doumazane, Etienne Trinquet, Eric Pin, Jean-Philippe Durroux, Thierry Front Endocrinol (Lausanne) Endocrinology The concept of oligomerization of G protein-coupled receptor (GPCR) opens new perspectives regarding physiological function regulation. The capacity of one GPCR to modify its binding and coupling properties by interacting with a second one can be at the origin of regulations unsuspected two decades ago. Although the concept is interesting, its validation at a physiological level is challenging and probably explains why receptor oligomerization is still controversial. Demonstrating direct interactions between two proteins is not trivial since few techniques present a spatial resolution allowing this precision. Resonance energy transfer (RET) strategies are actually the most convenient ones. During the last two decades, bioluminescent resonance energy transfer and time-resolved fluorescence resonance energy transfer (TR-FRET) have been widely used since they exhibit high signal-to-noise ratio. Most of the experiments based on GPCR labeling have been performed in cell lines and it has been shown that all GPCRs have the propensity to form homo- or hetero-oligomers. However, whether these data can be extrapolated to GPCRs expressed in native tissues and explain receptor functioning in real life, remains an open question. Native tissues impose different constraints since GPCR sequences cannot be modified. Recently, a fluorescent ligand-based GPCR labeling strategy combined to a TR-FRET approach has been successfully used to prove the existence of GPCR oligomerization in native tissues. Although the RET-based strategies are generally quite simple to implement, precautions have to be taken before concluding to the absence or the existence of specific interactions between receptors. For example, one should exclude the possibility of collision of receptors diffusing throughout the membrane leading to a specific FRET signal. The advantages and the limits of different approaches will be reviewed and the consequent perspectives discussed. Frontiers Research Foundation 2012-07-23 /pmc/articles/PMC3401989/ /pubmed/22837753 http://dx.doi.org/10.3389/fendo.2012.00092 Text en Copyright © Cottet, Faklaris, Maurel, Scholler, Doumazane, Trinquet, Pin and Durroux. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Endocrinology
Cottet, Martin
Faklaris, Orestis
Maurel, Damien
Scholler, Pauline
Doumazane, Etienne
Trinquet, Eric
Pin, Jean-Philippe
Durroux, Thierry
BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title_full BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title_fullStr BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title_full_unstemmed BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title_short BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues
title_sort bret and time-resolved fret strategy to study gpcr oligomerization: from cell lines toward native tissues
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401989/
https://www.ncbi.nlm.nih.gov/pubmed/22837753
http://dx.doi.org/10.3389/fendo.2012.00092
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