A mix-and-read fluorescence strategy for the switch-on probing of kinase activity based on an aptameric-peptide/graphene-oxide platform

Chem Asian J. 2014 Sep;9(9):2560-7. doi: 10.1002/asia.201402221. Epub 2014 Jul 22.

Abstract

Protein kinase plays a vital role in regulating signal-transduction pathways and its simple and quick detection is highly desirable because traditional kinase assays typically rely on a time-consuming kinase-phosphorylation process (ca. 1 h). Herein, we report a new and rapid fluorescence-based sensing platform for probing the activity of protein kinase that is based on the super-quenching capacity of graphene oxide (GO) nanosheets and specific recognition of the aptameric peptide (FITC-IP20). On the GO/peptide platform, the fluorescence quenching of FITC-IP20 that is adsorbed onto GO can be restored by selective binding of active protein kinase to the aptameric peptide, thereby resulting in the fast switch-on detection of kinase activity (ca. 15 min). The feasibility of this method has been demonstrated by the sensitive measurement of the activity of cAMP-dependent protein kinase (PKA), with a detection limit of 0.053 mU μL(-1). This assay technique was also successfully applied to the detection of kinase activation in cell lysate.

Keywords: biosensors; fluorescence; graphene; kinase; peptides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aptamers, Peptide / chemistry
  • Aptamers, Peptide / metabolism*
  • Biosensing Techniques*
  • Enzyme Activation
  • Fluorescence*
  • Fluorescent Dyes / chemistry
  • Fluorescent Dyes / metabolism*
  • Graphite / chemistry
  • Graphite / metabolism*
  • Humans
  • MCF-7 Cells
  • Oxides / chemistry
  • Oxides / metabolism*
  • Protein Kinases / chemistry
  • Protein Kinases / metabolism*
  • Spectrometry, Fluorescence
  • Tumor Cells, Cultured

Substances

  • Aptamers, Peptide
  • Fluorescent Dyes
  • Oxides
  • Graphite
  • Protein Kinases