Two-point kinetic experiments to quantify allosteric effects on radioligand dissociation

被引:78
作者
Kostenis, E [1 ]
Mohr, K [1 ]
机构
[1] UNIV BONN,INST PHARM,DEPT PHARMACOL & TOXICOL,D-53121 BONN,GERMANY
关键词
D O I
10.1016/0165-6147(96)10034-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Allosteric modulation of a receptor may be proved experimentally by demonstrating an altered radioligand dissociation in the presence of the allosteric modulator. Two-point kinetic experiments provide a screening-type approach to determine the delay of radioligand dissociation caused by allosteric modulation. In this article, Evi Kostenis and Klaus Mohr describe a pitfall in the data analysis that may lead to a suboptimum determination of the allosteric potency in the case of monophasic dissociations, and suggest how this problem may be resolved.
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页码:280 / 283
页数:4
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