Evidence map›Paper›PMID 35100990›Full record

ArticleBMC molecular and cell biology2022

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

Victoria Elisabeth Groß, Miron Mikhailowitsch Gershkovich, Torsten Schöneberg, Anette Kaiser, Simone Prömel

Abstract read
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Article in BMC molecular and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Victoria Elisabeth GroßRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, 04103, Leipzig, Germany.
Miron Mikhailowitsch GershkovichInstitute of Biochemistry, Faculty of Life Sciences, Leipzig University, 04103, Leipzig, Germany.
Torsten SchönebergRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, 04103, Leipzig, Germany.
Anette KaiserInstitute of Biochemistry, Faculty of Life Sciences, Leipzig University, 04103, Leipzig, Germany. anette.kaiser@uni-leipzig.de.
Simone PrömelRudolf Schönheimer Institute of Biochemistry, Medical Faculty, Leipzig University, 04103, Leipzig, Germany. proemel@uni-duesseldorf.de.ORCID http://orcid.org/0000-0001-7800-7323

Funding

Deutsche Forschungsgemeinschaft CRC 1423, project number 421152132, subproject B03Deutsche Forschungsgemeinschaft CRC 1423, project number 421152132, subproject C04Deutsche Forschungsgemeinschaft CRC 1423, project number 421152132, subproject Z03Deutsche Forschungsgemeinschaft FOR 2149, project number 265992651, project P02Sächsisches Staatsministerium für Wissenschaft und Kunst (DE) 100316655
6 · The paper itself

Abstract

backgroundProtein-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.

resultsWe 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.

conclusionsOur 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.

Indexed as

Caenorhabditis elegansReceptors, G-Protein-CoupledAnimalsEnergy TransferLigandsProtein TransportLigandsReceptors, G-Protein-CoupledC. elegansEnhanced bystander BRETNanoBRETReceptor-ligand interaction

Identifiers

PMID35100990
PMCPMC8805316

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.