| Literature DB >> 22015845 |
Ralf Schröder1, Johannes Schmidt, Stefanie Blättermann, Lucas Peters, Nicole Janssen, Manuel Grundmann, Wiebke Seemann, Dorina Kaufel, Nicole Merten, Christel Drewke, Jesus Gomeza, Graeme Milligan, Klaus Mohr, Evi Kostenis.
Abstract
Label-free dynamic mass redistribution (DMR) is a cutting-edge assay technology that enables real-time detection of integrated cellular responses in living cells. It relies on detection of refractive index alterations on biosensor-coated microplates that originate from stimulus-induced changes in the total biomass proximal to the sensor surface. Here we describe a detailed protocol to apply DMR technology to frame functional behavior of G protein-coupled receptors that are traditionally examined with end point assays on the basis of detection of individual second messengers, such as cAMP, Ca(2+) or inositol phosphates. The method can be readily adapted across diverse cellular backgrounds (adherent or suspension), including primary human cells. Real-time recordings can be performed in 384-well microtiter plates and be completed in 2 h, or they can be extended to several hours depending on the biological question to be addressed. The entire procedure, including cell harvesting and DMR detection, takes 1-2 d.Entities:
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Year: 2011 PMID: 22015845 DOI: 10.1038/nprot.2011.386
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491