G protein-coupled receptor internalization assays in the high-content screening format

被引:30
作者
Haasen, Dorothea [1 ]
Schnapp, Andreas
Valler, Martin J.
Heilker, Ralf
机构
[1] Boehringer Ingelheim Pharma GmbH & Co KG, Biberach, Germany
[2] Dept Pulm Res, Biberach, Germany
来源
MEASURING BIOLOGICAL RESPONSES WITH AUTOMATED MICROSCOPY | 2006年 / 414卷
关键词
D O I
10.1016/S0076-6879(06)14008-2
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
High-content screening (HCS), a combination of fluorescence microscopic imaging and automated image analysis, has become a frequently applied tool to study test compound effects in cellular disease-modeling systems. This chapter describes the measurement of G protein-coupled receptor (GPCR) internalization in the HCS format using a high-throughput, confocal cellular imaging device. GPCRs are the most successful group of therapeutic targets on the pharmaceutical market. Accordingly, the search for compounds that interfere with GPCR function in a specific and selective way is a major focus of the pharmaceutical industry today. This chapter describes methods for the ligand-induced internalization of GPCRs labeled previously with either a fluorophore-conjugated ligand or an antibody directed against an N-terminal tag of the GPCR. Both labeling techniques produce robust assay formats. Complementary to other functional GPCR drug discovery assays, internalization assays enable a pharmacological analysis of test compounds. We conclude that GPCR internalization assays represent a valuable medium/high-throughput screening format to determine the cellular activity of GPCR ligands.
引用
收藏
页码:121 / 139
页数:19
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