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NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells
by
Grätz, Lukas
, Bresinsky, Merlin
, Müller, Christoph
, Pockes, Steffen
, Tropmann, Katharina
, Bernhardt, Günther
in
631/1647
/ 631/45
/ 639/638
/ Drug development
/ Fluorescence
/ G protein-coupled receptors
/ Histamine
/ Histamine H2 receptors
/ Humanities and Social Sciences
/ Ligands
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
2020
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NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells
by
Grätz, Lukas
, Bresinsky, Merlin
, Müller, Christoph
, Pockes, Steffen
, Tropmann, Katharina
, Bernhardt, Günther
in
631/1647
/ 631/45
/ 639/638
/ Drug development
/ Fluorescence
/ G protein-coupled receptors
/ Histamine
/ Histamine H2 receptors
/ Humanities and Social Sciences
/ Ligands
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
2020
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells
by
Grätz, Lukas
, Bresinsky, Merlin
, Müller, Christoph
, Pockes, Steffen
, Tropmann, Katharina
, Bernhardt, Günther
in
631/1647
/ 631/45
/ 639/638
/ Drug development
/ Fluorescence
/ G protein-coupled receptors
/ Histamine
/ Histamine H2 receptors
/ Humanities and Social Sciences
/ Ligands
/ multidisciplinary
/ Science
/ Science (multidisciplinary)
2020
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NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells
Journal Article
NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells
2020
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Overview
Fluorescence/luminescence-based techniques play an increasingly important role in the development of test systems for the characterization of future drug candidates, especially in terms of receptor binding in the field of G protein-coupled receptors (GPCRs). In this article, we present the establishment of a homogeneous live cell-based BRET binding assay for the histamine H
2
receptor with different fluorescently labeled squaramide-type compounds synthesized in the course of this study. Py-1-labeled ligand
8
(UR-KAT478) was found to be most suitable in BRET saturation binding experiments with respect to receptor affinity (p
K
d
= 7.35) and signal intensity. Real-time kinetic experiments showed a full association of
8
within approximately 30 min and a slow dissociation of the ligand from the receptor. Investigation of reference compounds in BRET-based competition binding with
8
yielded p
K
i
values in agreement with radioligand binding data. This study shows that the BRET binding assay is a versatile test system for the characterization of putative new ligands at the histamine H
2
receptor and represents a valuable fluorescence-based alternative to canonical binding assays.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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