The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogs

被引:486
作者
Abramovitz, M
Adam, M
Boie, Y
Carrière, MC
Denis, D
Godbout, C
Lamontagne, S
Rochette, C
Sawyer, N
Tremblay, NM
Belley, M
Gallant, M
Dufresne, C
Gareau, Y
Ruel, R
Juteau, H
Labelle, M
Ouimet, N
Metters, KM
机构
[1] Merck Frosst Canada Inc, Merck Frosst Ctr Therapeut Res, Dept Biochem & Mol Biol, Pointe Claire, PQ H9R 4P8, Canada
[2] Merck Frosst Canada Inc, Merck Frosst Ctr Therapeut Res, Dept Med Chem, Pointe Claire, PQ H9R 4P8, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2000年 / 1483卷 / 02期
关键词
prostanoid receptor; prostaglandin; prostaglandin analog; radioligand binding; recombinant; human embryonic kidney; cell line;
D O I
10.1016/S1388-1981(99)00164-X
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
Stable cell lines that individually express the eight known human prostanoid receptors (EP1, EP2, EP3, EP4, DP, FP, IP and TP) have been established using human embryonic kidney (HEK) 293(EBNA) cells. These recombinant cell lines have been employed in radioligand binding assays to determine the equilibrium inhibitor constants of known prostanoid receptor ligands at these eight receptors. This has allowed, for the first time, an assessment of the affinity and selectivity of several novel compounds at the individual human prostanoid receptors. This information should facilitate interpretation of pharmacological studies that employ these ligands as tools to study human tissues and cell lines and should, therefore, result in a greater understanding of prostanoid receptor biology. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:285 / 293
页数:9
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