A cascade toehold-mediated strand displacement strategy for label-free and sensitive non-enzymatic recycling amplification detection of the HIV-1 gene

被引:21
|
作者
Li, Qiong [1 ,2 ]
Liu, Zhi [1 ]
Zhou, Danhua [2 ,3 ]
Pan, Jiafeng [2 ]
Liu, Chengshuai [4 ]
Chen, Junhua [2 ]
机构
[1] Hunan Agr Univ, Coll Biosci & Biotechnol, Changsha 410128, Hunan, Peoples R China
[2] Guangdong Inst Ecoenvironm & Sci & Technol, Guangdong Key Lab Integrated Agroenvironm Pollut, Guangzhou 510650, Guangdong, Peoples R China
[3] South China Agr Univ, Coll Nat Resources & Environm, Guangzhou 510462, Guangdong, Peoples R China
[4] Chinese Acad Sci, Inst Geochem, State Key Lab Environm Geochem, Guiyang 550081, Guizhou, Peoples R China
关键词
MOLECULAR MACHINE; CHAIN-REACTION; DNA; MICRORNA; BEACON;
D O I
10.1039/c8an02340a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a label-free fluorescence biosensor for simple detection of the HIV-1 gene was proposed by using toehold-mediated strand displacement reactions (TMSDRs) combined with a non-enzymatic target recycling amplification strategy. In this system, two TMSDRs were used. In the presence of the HIV-1 gene, an autocatalytic DNA machine can be activated. This leads to the generation of numerous free G-rich sequences, which can associate with a fluorescent dye N-methylmesoporphyrin IX (NMM) to yield an amplified fluorescence signal for the target detection. This sensing platform showed a high sensitivity towards the HIV-1 gene with a detection limit as low as 1.9 pM without any labelling, immobilization, or washing steps. The designed sensing system also exhibits an excellent selectivity for the HIV-1 gene compared with other interference DNA sequences. Furthermore, the presented biosensor is robust and has been successfully applied for the detection of the HIV-1 gene in a real biological sample with satisfactory results, suggesting that this method is promising for simple and early clinical diagnosis of HIV infection. Thanks to its simplicity, cost-effectiveness and ultrasensitivity, our proposed sensing strategy provides a universal platform for the detection of other genes by substituting the target-recognition element.
引用
收藏
页码:2173 / 2178
页数:6
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