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PMID: 1321566 Published · ppublish English Comparative Study Journal Article

Analysis of receptor binding displacement curves by a nonhomologous ligand, on the basis of an equivalent competition principle.

Analytical biochemistry ·Vol. 200 ·No. 2 ·1992-02-01 ·Pages 393-9

van Zoelen EJ

Abstract

An exact method for the analysis of receptor-ligand binding data when labeled bound ligand is displaced by a nonhomologous ligand with a different dissociation constant is described. The present method, which is based on an equivalent competition principle for the homologous and the nonhomologous ligand, converts displacement curves into a linear form and is also applicable to situations in which free concentrations of ligand are significantly smaller than the added concentrations as a result of ligand binding. It is shown that the dissociation constant of the nonhomologous ligand is given directly by the concentration of this nonhomologous ligand added and the free concentration of unlabeled homologous ligand required to give the same level of displacement of labeled bound ligand. On the basis of these displacement characteristics, all binding parameters for receptor interaction of the nonhomologous ligand can be obtained and expressed, for example, in a Scatchard plot. The present method, which is referred to as the equivalent competition method, is also evaluated in this study with respect to the effects of nonspecific ligand binding and the presence of multiple receptor classes.

MeSH Terms
Binding, Competitive Kinetics Ligands Mathematics Models, Theoretical Protein Binding Receptors, Cell Surface/metabolism Receptors, Drug/metabolism
Chemicals
Ligands Receptors, Cell Surface Receptors, Drug
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
van Zoelen E J
Department of Cell Biology, University of Nijmegen, The Netherlands.
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1992-02-01
Pages
393-9
Language
English
Region
United States
NLM ID
0370535
Subset
IM
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