Ultrasensitive electrochemical sensing platform based on graphene wrapping SnO2 nanocorals and autonomous cascade DNA duplication strategy

被引:29
作者
Chen, Ying-Xu [1 ,2 ,3 ]
Huang, Ke-Jing [1 ,2 ,3 ]
Lin, Feng [1 ,2 ,3 ]
Fang, Lin-Xia [1 ,2 ,3 ]
机构
[1] Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China
[2] Xinyang Normal Univ, Henan Prov Key Lab Utilizat Nonmetall Mineral Sou, Xinyang 464000, Peoples R China
[3] Xinyang Normal Univ, Inst Conservat & Utilizat Agrobioresources Dabie, Xinyang 464000, Peoples R China
基金
中国国家自然科学基金;
关键词
Stannic oxide nanocorals-graphene hybrids; Autonomous cascade DNA duplication strategy; Endonuclease; Polymerase; Signal amplification; NANOTUBE PASTE ELECTRODE; SIGNAL AMPLIFICATION; GOLD NANOPARTICLES; CARBON NANOTUBES; CHAIN-REACTION; ENZYME-FREE; SENSOR; OXIDE; SAMPLES; ACID;
D O I
10.1016/j.talanta.2017.07.042
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a sensitive, universal and reusable electrochemical biosensor based on stannic oxide nanocorals-graphene hybrids (SnO2 NCs-Gr) is developed for target DNA detection by using two kinds of DNA enzymes for signal amplification through an autonomous cascade DNA duplication strategy. A hairpin probe is designed composing of a projecting part at the 3'-end as identification sequence for target, a recognition site for nicking endonuclease, and an 18-carbon shim to stop polymerization process. The designed DNA duplication-incision-replacement process is handled by KF polymerase and endonuclease, then combining with gold nanoparticles as signal carrier for further signal amplification. In the detection system, the electrochemical-chemical-chemical procedure, which uses ferrocene methanol, tris(2-carboxyethyl)phosphine and L-ascorbic acid 2-phosphate as oxidoreduction neurogen, deoxidizer and zymolyte, separately, is applied to amplify detection signal. Benefiting from the multiple signal amplification mechanism, the proposed sensor reveals a good linear connection between the peak current and logarithm of analyte concentration in range of 0.0001-1 x 10(-11) mol L-1 with a detection limit of 1.25 x 10(-17) mol L-1 (S/N=3). This assay also opens one promising strategy for ultrasensitive determination of other biological molecules for bioanalysis and biomedicine diagnostics.
引用
收藏
页码:168 / 176
页数:9
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