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Stepwise Dosing Protocol for Increased Throughput in Label-Free Impedance-Based GPCR Assays.
Stolwijk, Judith A; Mildner, Anne-Kathrin; Kade, Christian; Skiba, Michael; Bernhardt, Guenther; Buschauer, Armin; Huebner, Harald; Gmeiner, Peter; Wegener, Joachim.
Afiliação
  • Stolwijk JA; Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.
  • Mildner AK; Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.
  • Kade C; Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.
  • Skiba M; Institute of Analytical Chemistry, Chemo- and Biosensors, University of Regensburg.
  • Bernhardt G; Institute of Pharmacy, University of Regensburg.
  • Buschauer A; Institute of Pharmacy, University of Regensburg.
  • Huebner H; Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg.
  • Gmeiner P; Department of Chemistry and Pharmacy, Friedrich-Alexander University Erlangen-Nuernberg.
  • 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.
J Vis Exp ; (156)2020 02 21.
Article em En | MEDLINE | ID: mdl-32150162
ABSTRACT
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).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bioensaio / Receptores Histamínicos / Transdução de Sinais / Histamina / Impedância Elétrica / Glioma Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bioensaio / Receptores Histamínicos / Transdução de Sinais / Histamina / Impedância Elétrica / Glioma Idioma: En Ano de publicação: 2020 Tipo de documento: Article