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A Versatile Sub-Nanomolar Fluorescent Ligand Enables NanoBRET Binding Studies and Single-Molecule Microscopy at the Histamine H3 Receptor.

Niklas RosierLukas GrätzHannes SchihadaJan MöllerAli IşbilirLaura J HumphrysMartin NaglUlla SeibelMartin J LohseSteffen Pockes
Published in: Journal of medicinal chemistry (2021)
The histamine H3 receptor (H3R) is considered an attractive drug target for various neurological diseases. We here report the synthesis of UR-NR266, a novel fluorescent H3R ligand. Broad pharmacological characterization revealed UR-NR266 as a sub-nanomolar compound at the H3R with an exceptional selectivity profile within the histamine receptor family. The presented neutral antagonist showed fast association to its target and complete dissociation in kinetic binding studies. Detailed characterization of standard H3R ligands in NanoBRET competition binding using UR-NR266 highlights its value as a versatile pharmacological tool to analyze future H3R ligands. The low nonspecific binding observed in all experiments could also be verified in TIRF and confocal microscopy. This fluorescent probe allows the highly specific analysis of native H3R in various assays ranging from optical high throughput technologies to biophysical analyses and single-molecule studies in its natural environment. An off-target screening at 14 receptors revealed UR-NR266 as a selective compound.
Keyphrases
  • single molecule
  • living cells
  • fluorescent probe
  • high throughput
  • binding protein
  • atomic force microscopy
  • case control
  • dna binding
  • high resolution
  • quantum dots
  • emergency department
  • high speed