PT  - JOURNAL ARTICLE
AU  - Sam R. J. Hoare
AU  - Gerda de Vries
AU  - Ted B. Usdin
TI  - Measurement of Agonist and Antagonist Ligand-Binding Parameters at the Human Parathyroid Hormone Type 1 Receptor: Evaluation of Receptor States and Modulation by Guanine Nucleotide
DP  - 1999 Jun 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 1323--1333
VI  - 289
IP  - 3
4099  - http://jpet.aspetjournals.org/content/289/3/1323.short
4100  - http://jpet.aspetjournals.org/content/289/3/1323.full
SO  - J Pharmacol Exp Ther1999 Jun 01; 289
AB  - Determination of ligand-binding constants for parathyroid hormone (PTH) receptors has been hampered by a lack of suitable experimental systems and mechanistic models for data analysis. In this study, ligand binding to the cloned human PTH-1 receptor was measured using membrane-based radioligand-binding assays. Guanosine 5′-O-(3-thiotriphosphate) (GTPγS) (10 μM) reduced binding of agonist radioligands [125I]rPTH(1–34) and [125I]PTHrP(1–36) but only to a limited extent (by 29 ± 5 and 42 ± 3%, respectively). Radiolabeled agonist dissociation was described by three and two phases in the absence and presence of GTPγS, respectively. GTPγS treatment removed a pseudoirreversible binding phase. Inhibition of radiolabeled antagonist ([125I]bPTH(3–34)) binding was measured using a 90-min incubation, which allowed binding of ligands to closely approach the asymptotic maximum. Agonist/[125I]bPTH(3–34) displacement curves were fitted best by assuming two independent affinity states, both in the presence and absence of GTPγS. After a 3-h incubation, binding of PTH agonists in the presence of GTPγS was described by a single affinity state, indicating the presence of slow components in the binding reaction. Antagonist binding was described by a single affinity state and was not significantly affected by GTPγS. The data were used to evaluate potential receptor-binding models. Although other models could not be excluded, all of the observations could be explained by assuming two binding sites on the receptor that recognize two corresponding sites on agonist ligands. Using the model, it was possible to estimate receptor-ligand-binding constants and to propose a direct method for identifying ligands that interact with a putative antagonist binding region of the receptor. U.S. Government