Radioligand Binding Studies: Pharmacological Profiles of Cloned Y-Receptor Subtypes
Karen McCrea, Herbert Herzog
Abstract
Karen McCrea, Herbert Herzog
Abstract
Radioligand binding is an extremely powerful technique that can provide detailed information about receptor-ligand interactions both in vitro and in vivo. Several types of binding assay can be performed, including studies of the kinetics of association or dissociation of the radiolabeled ligand, and equilibrium binding experiments such as saturation and competition binding assays. Data obtained from such studies generate accurate information regarding receptor number, ligand affinity, the existence of receptor subtypes, and allosteric interactions between binding sites and/or receptors. Generally receptorligand interactions are studied using membrane preparations since these give highly reproducible results. However, the technique can also be adapted to other preparations such as whole cells, tissue slices, solubilized receptors, and even whole animals. The techniques used and problems associated with radioligand binding studies are reviewed in ref. 1 . These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
OpenAlex reports 37 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Radioligand binding is an extremely powerful technique that can provide detailed information about receptor-ligand interactions both in vitro and in vivo. Several types of binding assay can be performed, including studies of the kinetics of association or dissociation of the radiolabeled ligand, and equilibrium binding experiments such as saturation and competition binding assays. Data obtained from such studies generate accurate information regarding receptor number, ligand affinity, the existence of receptor subtypes, and allosteric interactions between binding sites and/or receptors. Generally receptorligand interactions are studied using membrane preparations since these give highly reproducible results. However, the technique can also be adapted to other preparations such as whole cells, tissue slices, solubilized receptors, and even whole animals. The techniques used and problems associated with radioligand binding studies are reviewed in ref. 1 . These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
Key concepts: Radioligand, Radioligand Assay, Receptor, Allosteric regulation, Ligand (biochemistry), In vivo, Receptor–ligand kinetics, Biophysics