A fluorescence assay for microRNA let-7a by a double-stranded DNA modified gold nanoparticle nanoprobe combined with graphene oxide

被引:21
作者
Gao, Yuanyuan [1 ]
Tian, Jingjing [1 ]
Zhang, Xing [1 ]
Qiao, Bin [2 ,3 ,4 ]
Cao, Yang [5 ]
Wang, Xiaohong [1 ]
Wu, Qiang [2 ,3 ,4 ]
机构
[1] Hainan Univ, Coll Mat Sci & Engn, State Key Lab Marine Resource Utilizat South Chin, Haikou 570228, Hainan, Peoples R China
[2] Hainan Med Univ, Key Lab Emergency & Trauma, Minist Educ, Haikou 571199, Hainan, Peoples R China
[3] Hainan Med Univ, Res Unit Isl Emergency Med, Chinese Acad Med Sci, Haikou 571199, Hainan, Peoples R China
[4] Hainan Med Univ, Sch Trop Med & Lab Med, Haikou 571199, Hainan, Peoples R China
[5] Qiongtai Normal Univ, Haikou 571127, Hainan, Peoples R China
基金
中国国家自然科学基金;
关键词
REAL-TIME PCR; ELECTROCHEMICAL DETECTION; AMPLIFICATION; EXPRESSION; BIOSENSOR; DIAGNOSIS; CANCER;
D O I
10.1039/c9an02274k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Graphene oxide (GO) is capable of quenching fluorescence in bound fuel single stranded DNA (ssDNA) labeled with dye. In the presence of target microRNA let-7a, two cascaded toehold-mediated strand displacement reactions (TSDRs) were triggered, thereby desorbing substantial pi-pi stacking adsorbed fuel DNA from GO through recycling amplification, simultaneously accompanied with the restoration of dye fluorescence. By coupling dsDNA-AuNPs with the GO nanosheet, the proposed strategy achieved a non-enzymatic sensitive assay with a low detection limit of 3.9 pM. Hence, the proposed approach has great potential for applications in early cancer diagnosis and clinical analysis.
引用
收藏
页码:1190 / 1194
页数:5
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