Abstract
The radioligand binding assay is a relatively simple but powerful tool for studying G protein-coupled receptors. There are three basic types of radioligand binding experiments: (1) saturation experiments from which the affinity of the radioligand for the receptor and the binding site density can be determined; (2) inhibition experiments from which the affinity of a competing, unlabeled compound for the receptor can be determined; and (3) kinetic experiments from which the forward and reverse rate constants for radioligand binding can be determined. Detailed methods for typical radioligand binding assays for G protein-coupled receptors in membranes and intact cells are presented for these types of experiments. Detailed procedures for analysis of the data obtained from these experiments are also given.
Original language | English (US) |
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Pages (from-to) | 135-164 |
Number of pages | 30 |
Journal | Methods in Molecular Biology |
Volume | 746 |
DOIs | |
State | Published - 2011 |
Keywords
- Affinity
- Assay
- Binding
- Competition
- G protein-coupled receptor
- Inhibition
- Intact cell
- Kinetic
- Non-specific binding
- Radioligand
- Radioreceptor
- Rate constant
- Receptor
- Saturation
ASJC Scopus subject areas
- Molecular Biology
- Genetics