FRET-based screening assay using small-molecule photoluminescent probes in lysate of cells overexpressing RFP-fused protein kinases

被引:11
作者
Manoharan, Ganesh Babu [1 ]
Enkvist, Erki [1 ]
Kasari, Marje [1 ]
Viht, Kaido [1 ]
Zenn, Michael [2 ]
Prinz, Anke [2 ]
Filhol, Odile [3 ,4 ,5 ]
Herberg, Friedrich W. [2 ]
Uri, Asko [1 ]
机构
[1] Univ Tartu, Inst Chem, EE-50411 Tartu, Estonia
[2] Univ Kassel, Dept Biochem, D-34132 Kassel, Germany
[3] INSERM, U1036, Grenoble, France
[4] CEA Grenoble, Inst Life Sci Res & Technol, Biol Canc & Infect, F-38054 Grenoble, France
[5] Univ Grenoble Alpes, Unite Mixte Rech, Grenoble, France
关键词
Protein kinases; Cell lysate; FRET; TR FRET; Red fluorescent protein; Photo luminescent probes; RESONANCE ENERGY-TRANSFER; RED FLUORESCENT PROTEIN; LIVING CELLS; MONOMERIC RED; BINDING ASSAY; CYCLIC-AMP; INHIBITORS; LIFETIME;
D O I
10.1016/j.ab.2015.04.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An assay was developed for the characterization of protein kinase inhibitors in lysates of mammalian cells based on the measurement of FRET between overexpressed red fluorescent protein (TagRFP)-fused protein kinases (PKs) and luminophore-labeled small-molecule inhibitors (ARC-Photo probes). Two types of the assay, one using TagRFP as the photoluminescence donor together with ARC-Photo probes containing a red fluorophore dye as acceptor, and the other using TagRFP as the acceptor fluorophore in combination with a terbium cryptate-based long-lifetime photoluminescence donor, were used for FRET-based measurements in lysates of the cells overexpressing TagRFP-fused PKs. The second variant of the assay enabled the performance of the measurements under time-resolved conditions that led to substantially higher values of the signal/background ratio and further improved the reliability of the assay. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:10 / 17
页数:8
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