Validation of extracellular ligand–receptor interactions by Flow-TriCEPS
Abstract 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 fas...
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doaj-073e258a42e047c091f749720d485b932020-11-25T02:04:08ZengBMCBMC Research Notes1756-05002018-12-011111710.1186/s13104-018-3974-5Validation of extracellular ligand–receptor interactions by Flow-TriCEPSLaura A. Lopez-Garcia0Levent Demiray1Sandra Ruch-Marder2Ann-Katrin Hopp3Michael O. Hottiger4Paul M. Helbling5Maria P. Pavlou6Dualsystems Biotech A.G.Dualsystems Biotech A.G.Dualsystems Biotech A.G.Department of Molecular Mechanisms of Disease, University of ZurichDepartment of Molecular Mechanisms of Disease, University of ZurichDualsystems Biotech A.G.Dualsystems Biotech A.G.Abstract 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.http://link.springer.com/article/10.1186/s13104-018-3974-5Flow-TriCEPSHATRICLRCKnock downsiRNACandidate verification |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Laura A. Lopez-Garcia Levent Demiray Sandra Ruch-Marder Ann-Katrin Hopp Michael O. Hottiger Paul M. Helbling Maria P. Pavlou |
spellingShingle |
Laura A. Lopez-Garcia Levent Demiray Sandra Ruch-Marder Ann-Katrin Hopp Michael O. Hottiger Paul M. Helbling Maria P. Pavlou Validation of extracellular ligand–receptor interactions by Flow-TriCEPS BMC Research Notes Flow-TriCEPS HATRIC LRC Knock down siRNA Candidate verification |
author_facet |
Laura A. Lopez-Garcia Levent Demiray Sandra Ruch-Marder Ann-Katrin Hopp Michael O. Hottiger Paul M. Helbling Maria P. Pavlou |
author_sort |
Laura A. Lopez-Garcia |
title |
Validation of extracellular ligand–receptor interactions by Flow-TriCEPS |
title_short |
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_sort |
validation of extracellular ligand–receptor interactions by flow-triceps |
publisher |
BMC |
series |
BMC Research Notes |
issn |
1756-0500 |
publishDate |
2018-12-01 |
description |
Abstract 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. |
topic |
Flow-TriCEPS HATRIC LRC Knock down siRNA Candidate verification |
url |
http://link.springer.com/article/10.1186/s13104-018-3974-5 |
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