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Indexed by:Journal Papers

Date of Publication:2015-06-15

Journal:BIOSENSORS & BIOELECTRONICS

Included Journals:SCIE、EI、PubMed、Scopus

Volume:68

Page Number:7-13

ISSN No.:0956-5663

Key Words:Graphene/Au-NPs hybrid; hOGG1; Colorimetric; Enzyme mimetic

Abstract:A sensitive, rapid and label-free assay for calorimetric detection of human 8-hydroxyguanine glycosylase (hOGG1) was proposed based on the tunable catalytic ability of graphene/gold nanoparticles (graphene/Au-NPs) hybrids and the terminal protection of hOGG1. In presence of H2O2, the hybrids were capable of catalyzing the oxidation of color developing reagent, causing a concomitant change in color. Due to the excellent controllability, the capacity could be inhibited by adsorption of ssDNA onto the hybrids sheets and recovered when the adsorbed ssDNA was digested by exonuclease. The terminal protection of hOGG1 could irreversibly interrupt the digestion of the captured ssDNA (containing the oxidative damage site) by the exonuclease, thus preventing the catalytic ability of graphene/Au-NPs from being recovered. The original color change which related to the concentration of the protected ssDNA facilitated quantitative detection of hOGG1 activity. Compared with conventional methods for hOGG1 detection, the presented assay without any labeling process greatly simplified the operation steps and reduced the analysis time. This approach performed a linear response for hOGG1 activity from 0.02 to 0.11 U/mu L, with a detection limit of 0.0016 U/mu L, and realized the quantification of hOGG1 activity in real cell lines. (C) 2015 Elsevier B.V. All rights reserved.