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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Main Authors: Laura A. Lopez-Garcia, Levent Demiray, Sandra Ruch-Marder, Ann-Katrin Hopp, Michael O. Hottiger, Paul M. Helbling, Maria P. Pavlou
Format: Article
Language:English
Published: BMC 2018-12-01
Series:BMC Research Notes
Subjects:
LRC
Online Access:http://link.springer.com/article/10.1186/s13104-018-3974-5
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spelling 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
work_keys_str_mv AT lauraalopezgarcia validationofextracellularligandreceptorinteractionsbyflowtriceps
AT leventdemiray validationofextracellularligandreceptorinteractionsbyflowtriceps
AT sandraruchmarder validationofextracellularligandreceptorinteractionsbyflowtriceps
AT annkatrinhopp validationofextracellularligandreceptorinteractionsbyflowtriceps
AT michaelohottiger validationofextracellularligandreceptorinteractionsbyflowtriceps
AT paulmhelbling validationofextracellularligandreceptorinteractionsbyflowtriceps
AT mariappavlou validationofextracellularligandreceptorinteractionsbyflowtriceps
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