Use of a new proximity assay (NanoBRET) to investigate the ligand‐binding characteristics of three fluorescent ligands to the human β 1 ‐adrenoceptor expressed in HEK‐293 cells
Author:
Affiliation:
1. Cell Signalling and Pharmacology Research Group School of Life Sciences University of Nottingham Nottingham NG7 2UH United Kingdom
2. Heptares Therapeutics Ltd. Bio Park Welwyn Garden City AL7 3AX United Kingdom
Funder
Medical Research Council
University of Nottingham
Publisher
Wiley
Subject
General Pharmacology, Toxicology and Pharmaceutics,Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/prp2.250
Reference31 articles.
1. Site of Action of β-Ligands at the Human β1-Adrenoceptor
2. Agonist Actions of “β-Blockers” Provide Evidence for Two Agonist Activation Sites or Conformations of the Human β1-Adrenoceptor
3. Role of Key Transmembrane Residues in Agonist and Antagonist Actions at the Two Conformations of the Human β1-Adrenoceptor
4. Synthesis and Characterization of High-Affinity 4,4-Difluoro-4-bora-3a,4a-diaza-s-indacene-Labeled Fluorescent Ligands for Human β-Adrenoceptors
5. Identification of Key Residues in Transmembrane 4 Responsible for the Secondary, Low-Affinity Conformation of the Humanβ1-Adrenoceptor
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