机构:
INSERM, U1036, Grenoble, France
CEA Grenoble, Inst Life Sci Res & Technol, Biol Canc & Infect, F-38054 Grenoble, France
Univ Grenoble Alpes, Unite Mixte Rech, Grenoble, FranceUniv Tartu, Inst Chem, EE-50411 Tartu, Estonia
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.