Fluorescent detection of protein kinase based on positively charged gold nanoparticles
Herein, we report a fluorometric method for monitoring the activity and inhibition of protein kinase based on positively charged gold nanoparticles, (+)AuNPs. In this assay, when the cationic substrate peptide (S-peptide) is phosphorylated by protein kinase, the resulting negatively charged product...
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Veröffentlicht in: | Talanta (Oxford) 2014-10, Vol.128, p.360-365 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Herein, we report a fluorometric method for monitoring the activity and inhibition of protein kinase based on positively charged gold nanoparticles, (+)AuNPs. In this assay, when the cationic substrate peptide (S-peptide) is phosphorylated by protein kinase, the resulting negatively charged product peptide (P-peptide) will be adsorbed onto (+)AuNPs through electrostatic interaction, and the fluorescence of fluorescein isothiocyanate (FITC) on the peptide will be quenched by (+)AuNPs. Thus, the fluorescence of solution can respond to the activity of protein kinase. The feasibility of this (+)AuNPs-based method has been demonstrated by sensitive measurement of the activity of cAMP-dependent protein kinase (PKA) with a low detection limit (0.5mUμL−1). Furthermore, the system is successfully applied to estimate the IC50 value of PKA inhibitor H-89. The fast mix-and-readout detection process as well as the simple synthesis of the unmodified (+)AuNPs makes this proposed method a promising candidate for simple and cost-effective kinase activity detection and a good potential in high-throughput screening of kinase-related drugs.
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•A simple method for protein kinase activity analysis based on (+)AuNPs is presented.•(+)AuNPs can fast, selectively, and sensitively recognize P-peptide from S-peptide.•(+)AuNPs are first and successfully used to detect the activity and inhibition of PKA.•The unmodified (+)AuNPs are easily synthesized. |
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ISSN: | 0039-9140 1873-3573 |
DOI: | 10.1016/j.talanta.2014.04.061 |