Homogeneous Electrochemical Assay for Real-time Monitoring of Exonuclease III Activity Based on a Graphene Monolayer

被引:10
作者
Lee, Heon-Kyu [1 ]
Heo, Jihye [1 ]
Myung, Sung [2 ]
Shin, Ik-Soo [3 ]
Kim, Tae Hyun [1 ]
机构
[1] Soonchunhyang Univ, Dept Chem, Asan 31538, South Korea
[2] Korea Res Inst Chem Technol, Thin Film Mat Res Ctr, Daejeon 34114, South Korea
[3] Soongsil Univ, Dept Chem, Seoul 06978, South Korea
基金
新加坡国家研究基金会;
关键词
Electrochemical assay; exonuclease III activity assay; Exo III; graphene monolayer; real-time; drug screening; inhibition assay; RECYCLING AMPLIFICATION; LUPUS-ERYTHEMATOSUS; WERNER-SYNDROME; DNA; TREX1; OXIDE; ADSORPTION; DESORPTION; MUTATIONS; LANGMUIR;
D O I
10.1002/elan.201700006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A homogeneous electrochemical assay based on a graphene monolayer electrode was developed for simple, sensitive, rapid and quantitative analysis of the exonuclease III (Exo III) activity. The method utilized a methylene blue (MB) tagged DNA substrate with hairpin structure, and a graphene monolayer attached on the working electrode. Before digestion, the hairpin structure prevents the adsorption of the DNA substrate to the graphene surface. Degradation of the substrate by the 3'-5' Exo III, however, yields single-stranded DNA (ssDNA), resulting in its subsequent binding to the graphene surface through pi-pi stacking, which produces the voltammetric current from electrochemical reduction of the MB tag anchoring at the end of ssDNA. A direct quantification of the Exo III activity can be achieved by measuring the reductive peak current of the MB tag under easily attainable potential (similar to -0.1V vs Ag/AgCl) range comparably sensitive to the conventional methods such as a gel-based or fluorescence-based assays. Our approach can be applied to measure various exonucleases activity by adjusting the structure of DNA substrate suggesting a new assay method in drug screening and basic research related to the enzymes.
引用
收藏
页码:1749 / 1754
页数:6
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