Stepwise Dosing Protocol for Increased Throughput in Label-Free Impedance-Based GPCR Assays.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
21 02 2020
Historique:
entrez: 10 3 2020
pubmed: 10 3 2020
medline: 25 8 2020
Statut: epublish

Résumé

Label-free impedance-based assays are increasingly used to non-invasively study ligand-induced GPCR activation in cell culture experiments. The approach provides real-time cell monitoring with a device-dependent time resolution down to several tens of milliseconds and it is highly automated. However, when sample numbers get high (e.g., dose-response studies for various different ligands), the cost for the disposable electrode arrays as well as the available time resolution for sequential well-by-well recordings may become limiting. Therefore, we here present a serial agonist addition protocol which has the potential to significantly increase the output of label-free GPCR assays. Using the serial agonist addition protocol, a GPCR agonist is added sequentially in increasing concentrations to a single cell layer while continuously monitoring the sample's impedance (agonist mode). With this serial approach, it is now possible to establish a full dose-response curve for a GPCR agonist from just one single cell layer. The serial agonist addition protocol is applicable to different GPCR coupling types, Gq Gi/0 or Gs and it is compatible with recombinant and endogenous expression levels of the receptor under study. Receptor blocking by GPCR antagonists is assessable as well (antagonist mode).

Identifiants

pubmed: 32150162
doi: 10.3791/60686
doi:

Substances chimiques

Ligands 0
Receptors, Histamine 0
Histamine 820484N8I3

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Judith A Stolwijk (JA)

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.

Anne-Kathrin Mildner (AK)

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.

Christian Kade (C)

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.

Michael Skiba (M)

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.

Guenther Bernhardt (G)

Institute of Pharmacy, University of Regensburg.

Armin Buschauer (A)

Institute of Pharmacy, University of Regensburg.

Harald Huebner (H)

Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg.

Peter Gmeiner (P)

Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg.

Joachim Wegener (J)

Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg; Fraunhofer Research Institution for Microsystems and Solid State Technologies EMFT; joachim.wegener@ur.de.

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Classifications MeSH