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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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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. |
format | Online Article Text |
id | pubmed-8805316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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