Development of a time-resolved fluorescence probe for evaluation of competitive binding to the cholecystokinin 2 receptor

被引:0
|
作者
Elshan, N. G. R. Dayan [1 ]
Jayasundera, Thanuja [2 ]
Weber, Craig S. [2 ]
Lynch, Ronald M. [2 ,3 ]
Mash, Eugene A. [1 ]
机构
[1] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Physiol, Tucson, AZ 85724 USA
[3] Univ Arizona, Inst Bio5, Tucson, AZ 85721 USA
关键词
Multivalent binding; Cholecystokinin; 2; receptor; High-throughput screening; Time-resolved fluorescence; Dissociation-enhanced lanthanide fluoroimmunoassay; MELANOCORTIN RECEPTORS; MULTIVALENT APPROACH; B RECEPTOR; PEPTIDES; LIGAND; CANCER; ASSAY; IONS;
D O I
10.1016/j.bmc.2015.02.028
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis, characterization, and use of Eu-DTPA-PEGO-Trp-Nle-Asp-Phe-NH2 (Eu-DTPA-PEGO-CCK4), a luminescent probe targeted to cholecystokinin 2 receptor (CCK2R, aka CCKBR), are described. The probe was prepared by solid phase synthesis. A K-d value of 17 +/- 2 nM was determined by means of saturation binding assays using HEK-293 cells that overexpress CCK2R. The probe was then used in competitive binding assays against Ac-CCK4 and three new trivalent CCK4 compounds. Repeatable and reproducible binding assay results were obtained. Given its ease of synthesis, purification, receptor binding properties, and utility in competitive binding assays, Eu-DTPA-PEGO-CCK4 could become a standard tool for high-throughput screening of compounds in development targeted to cholecystokinin receptors. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1841 / 1848
页数:8
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