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Label-free fluorescent detection of protein kinase activity based on the aggregation behavior of unmodified quantum dots.

Authors
  • Xu, Xiahong
  • Liu, Xin
  • Nie, Zhou
  • Pan, Yuliang
  • Guo, Manli
  • Yao, Shouzhuo
Type
Published Article
Journal
Analytical Chemistry
Publisher
American Chemical Society
Publication Date
Jan 01, 2011
Volume
83
Issue
1
Pages
52–59
Identifiers
DOI: 10.1021/ac102786c
PMID: 21128608
Source
Medline
License
Unknown

Abstract

Herein, we present a novel label-free fluorescent assay for monitoring the activity and inhibition of protein kinases based on the aggregation behavior of unmodified CdTe quantum dots (QDs). In this assay, cationic substrate peptides induce the selective aggregation of unmodified QDs with anionic surface charge, whereas phosphorylated peptides do not. Phosphorylation by kinase alters the net charge of peptides and subsequently inhibits the aggregation of unmodified QDs, causing an enhanced fluorescence with a 45 nm blue-shift in emission and a yellow-to-green emission color change. Hence the fluorescence response allows this QD-based method to easily probe kinase activity by a spectrometer or even by the naked eye. The feasibility of the method has been demonstrated by sensitive measurement of the activity of cAMP-dependent protein kinase (PKA) with a low detection limit (0.47 mU μL(-1)). On the basis of the fluorescence response of QDs on the concentration of PKA inhibitor H-89, the IC(50) value, the half maximal inhibitory concentration, was estimated, which was in agreement with the literature value. Moreover, the system can be applicable to detect the Forskolin/3-isobutyl-1-methylxantine (IBMX)-stimulated activation of PKA in cell lysate. Unlike the existing QD-based enzyme activity assays in which the modification process of QDs is essential, this method relies on unmodified QDs without the requirement of peptide labeling and QDs' modification, presenting a promising candidate for cost-effective kinase activity and inhibitor screening assays.

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