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NanoBRET in C. elegans illuminates functional receptor interactions in real time

BACKGROUND: Protein-protein interactions form the basis of every organism and thus, investigating their dynamics, intracellular protein localization, trafficking and interactions of distinct proteins such as receptors and their ligand-binding are of general interest. Bioluminescence resonance energy...

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Autores principales: Groß, Victoria Elisabeth, Gershkovich, Miron Mikhailowitsch, Schöneberg, Torsten, Kaiser, Anette, Prömel, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805316/
https://www.ncbi.nlm.nih.gov/pubmed/35100990
http://dx.doi.org/10.1186/s12860-022-00405-w
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author Groß, Victoria Elisabeth
Gershkovich, Miron Mikhailowitsch
Schöneberg, Torsten
Kaiser, Anette
Prömel, Simone
author_facet Groß, Victoria Elisabeth
Gershkovich, Miron Mikhailowitsch
Schöneberg, Torsten
Kaiser, Anette
Prömel, Simone
author_sort Groß, Victoria Elisabeth
collection PubMed
description BACKGROUND: Protein-protein interactions form the basis of every organism and thus, investigating their dynamics, intracellular protein localization, trafficking and interactions of distinct proteins such as receptors and their ligand-binding are of general interest. Bioluminescence resonance energy transfer (BRET) is a powerful tool to investigate these aspects in vitro. Since in vitro approaches mostly neglect the more complex in vivo situation, we established BRET as an in vivo tool for studying protein interactions in the nematode C. elegans. RESULTS: We generated worms expressing NanoBRET sensors and elucidated the interaction of two ligand-G protein-coupled receptor (GPCR) pairs, the neuropeptide receptor NPR-11 and the Adhesion GPCR LAT-1. Furthermore, we adapted the enhanced bystander BRET technology to measure subcellular protein localization. Using this approach, we traced ligand-induced internalization of NPR-11 in vivo. CONCLUSIONS: Our results indicate that in vivo NanoBRET is a tool to investigate specific protein interactions and localization in a physiological setting in real time in the living organism C. elegans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12860-022-00405-w.
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spelling pubmed-88053162022-02-03 NanoBRET in C. elegans illuminates functional receptor interactions in real time Groß, Victoria Elisabeth Gershkovich, Miron Mikhailowitsch Schöneberg, Torsten Kaiser, Anette Prömel, Simone BMC Mol Cell Biol Research Article BACKGROUND: Protein-protein interactions form the basis of every organism and thus, investigating their dynamics, intracellular protein localization, trafficking and interactions of distinct proteins such as receptors and their ligand-binding are of general interest. Bioluminescence resonance energy transfer (BRET) is a powerful tool to investigate these aspects in vitro. Since in vitro approaches mostly neglect the more complex in vivo situation, we established BRET as an in vivo tool for studying protein interactions in the nematode C. elegans. RESULTS: We generated worms expressing NanoBRET sensors and elucidated the interaction of two ligand-G protein-coupled receptor (GPCR) pairs, the neuropeptide receptor NPR-11 and the Adhesion GPCR LAT-1. Furthermore, we adapted the enhanced bystander BRET technology to measure subcellular protein localization. Using this approach, we traced ligand-induced internalization of NPR-11 in vivo. CONCLUSIONS: Our results indicate that in vivo NanoBRET is a tool to investigate specific protein interactions and localization in a physiological setting in real time in the living organism C. elegans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12860-022-00405-w. BioMed Central 2022-01-31 /pmc/articles/PMC8805316/ /pubmed/35100990 http://dx.doi.org/10.1186/s12860-022-00405-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Groß, Victoria Elisabeth
Gershkovich, Miron Mikhailowitsch
Schöneberg, Torsten
Kaiser, Anette
Prömel, Simone
NanoBRET in C. elegans illuminates functional receptor interactions in real time
title NanoBRET in C. elegans illuminates functional receptor interactions in real time
title_full NanoBRET in C. elegans illuminates functional receptor interactions in real time
title_fullStr NanoBRET in C. elegans illuminates functional receptor interactions in real time
title_full_unstemmed NanoBRET in C. elegans illuminates functional receptor interactions in real time
title_short NanoBRET in C. elegans illuminates functional receptor interactions in real time
title_sort nanobret in c. elegans illuminates functional receptor interactions in real time
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805316/
https://www.ncbi.nlm.nih.gov/pubmed/35100990
http://dx.doi.org/10.1186/s12860-022-00405-w
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