Highly Sensitive Multiple microRNA Detection Based on Fluorescence Quenching of Graphene Oxide and Isothermal Strand-Displacement Polymerase Reaction

被引:265
作者
Dong, Haifeng [2 ]
Zhang, Jing [1 ,3 ]
Ju, Huangxian [1 ]
Lu, Huiting [2 ]
Wang, Shiyan [2 ]
Jin, Shi [2 ]
Hao, Kaihong [2 ]
Du, Hongwu [2 ]
Zhang, Xueji [2 ]
机构
[1] Nanjing Univ, Dept Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Peoples R China
[2] Univ Sci & Technol Beijing, Res Ctr Bioengn & Sensing Technol, Beijing 100083, Peoples R China
[3] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
COLORIMETRIC DETECTION; SENSING BIOMOLECULES; GOLD NANOPARTICLES; OPTICAL-PROPERTIES; GENE-EXPRESSION; NORTHERN BLOT; DNA; HYBRIDIZATION; PROBES; RNAS;
D O I
10.1021/ac300721u
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
A simple, highly sensitive, and selective multiple microRNA (miRNA) detection method based on the graphene oxide (GO) fluorescence quenching and isothermal strand-displacement polymerase reaction (ISDPR) was proposed. The capability to discriminate ssDNA and double-stranded nucleic acid structure coupled with the extraordinary fluorescence quenching of GO on multiple organic dye allows the proposed strategy to simultaneously and selectively detect several miRNA labeled with different dyes in the same solution, while the ISDPR amplification endows the detection method with high sensitivity. The strong interaction between ssDNA and GO led to the fluorescent ssDNA probe exhibiting minimal background fluorescence. Upon the recognition of specific target miRNA, an ISDPR was triggered to produce numerous massive specific DNA-miRNA duplex helixes, and a strong emission was observed due to the weak interaction between the DNA-miRNA duplex helix and GO. A miRNA biosensor down to 2.1 fM with a linear range of 4 orders of magnitude was obtained. Furthermore, the large planar surface of GO allows simultaneous quenching of several DNA probes with different dyes and produces a multiple biosensing platform with high sensitivity and selectivity, which has promising application in profiling the pattern of miRNA expression and biomedical research.
引用
收藏
页码:4587 / 4593
页数:7
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