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Validation of extracellular ligand–receptor interactions by Flow-TriCEPS
OBJECTIVE: The advent of ligand-based receptor capture methodologies, allows the identification of unknown receptor candidates for orphan extracellular ligands. However, further target validation can be tedious, laborious and time-consuming. Here, we present a methodology that provides a fast and co...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280402/ https://www.ncbi.nlm.nih.gov/pubmed/30518414 http://dx.doi.org/10.1186/s13104-018-3974-5 |
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author | Lopez-Garcia, Laura A. Demiray, Levent Ruch-Marder, Sandra Hopp, Ann-Katrin Hottiger, Michael O. Helbling, Paul M. Pavlou, Maria P. |
author_facet | Lopez-Garcia, Laura A. Demiray, Levent Ruch-Marder, Sandra Hopp, Ann-Katrin Hottiger, Michael O. Helbling, Paul M. Pavlou, Maria P. |
author_sort | Lopez-Garcia, Laura A. |
collection | PubMed |
description | OBJECTIVE: The advent of ligand-based receptor capture methodologies, allows the identification of unknown receptor candidates for orphan extracellular ligands. However, further target validation can be tedious, laborious and time-consuming. Here, we present a methodology that provides a fast and cost-efficient alternative for candidate target verification on living cells. RESULTS: In the described methodology a ligand of interest (e.g. transferrin, epidermal growth factor or insulin) was conjugated to a linker (TriCEPS) that carries a biotin. To confirm ligand/receptor interactions, the ligand–TriCEPS conjugates were first added onto living cells and cells were subsequently labeled with a streptavidin-fluorophore and analyzed by flow cytometry (thus referred as Flow-TriCEPS). Flow-TriCEPS was also used to validate identified receptor candidates when combined with a siRNA knock down approach (i.e. reduction of expression levels). This approach is versatile as it can be applied for different classes of ligands (proteins, peptides, antibodies) and different cell lines. Moreover, the method is time-efficient since it takes advantage of the large variety of commercially available (and certified) siRNAs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3974-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6280402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62804022018-12-10 Validation of extracellular ligand–receptor interactions by Flow-TriCEPS Lopez-Garcia, Laura A. Demiray, Levent Ruch-Marder, Sandra Hopp, Ann-Katrin Hottiger, Michael O. Helbling, Paul M. Pavlou, Maria P. BMC Res Notes Research Note OBJECTIVE: The advent of ligand-based receptor capture methodologies, allows the identification of unknown receptor candidates for orphan extracellular ligands. However, further target validation can be tedious, laborious and time-consuming. Here, we present a methodology that provides a fast and cost-efficient alternative for candidate target verification on living cells. RESULTS: In the described methodology a ligand of interest (e.g. transferrin, epidermal growth factor or insulin) was conjugated to a linker (TriCEPS) that carries a biotin. To confirm ligand/receptor interactions, the ligand–TriCEPS conjugates were first added onto living cells and cells were subsequently labeled with a streptavidin-fluorophore and analyzed by flow cytometry (thus referred as Flow-TriCEPS). Flow-TriCEPS was also used to validate identified receptor candidates when combined with a siRNA knock down approach (i.e. reduction of expression levels). This approach is versatile as it can be applied for different classes of ligands (proteins, peptides, antibodies) and different cell lines. Moreover, the method is time-efficient since it takes advantage of the large variety of commercially available (and certified) siRNAs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3974-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-05 /pmc/articles/PMC6280402/ /pubmed/30518414 http://dx.doi.org/10.1186/s13104-018-3974-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Note Lopez-Garcia, Laura A. Demiray, Levent Ruch-Marder, Sandra Hopp, Ann-Katrin Hottiger, Michael O. Helbling, Paul M. Pavlou, Maria P. Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title | Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_full | Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_fullStr | Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_full_unstemmed | Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_short | Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_sort | validation of extracellular ligand–receptor interactions by flow-triceps |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280402/ https://www.ncbi.nlm.nih.gov/pubmed/30518414 http://dx.doi.org/10.1186/s13104-018-3974-5 |
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