A linear DNA probe as an alternative to a molecular beacon for improving the sensitivity of a homogenous fluorescence biosensing platform for DNA detection using target-primed rolling circle amplification

被引:23
|
作者
Zhou, Fulin [1 ]
Li, Baoxin [1 ]
Ma, Jiyuan [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Analyt Chem Life Sci Shaanxi Prov, Xian 710062, Peoples R China
来源
RSC ADVANCES | 2015年 / 5卷 / 06期
基金
中国国家自然科学基金;
关键词
MULTIPLEXED DETECTION; AMPLIFIED SYNTHESIS; NUCLEIC-ACIDS; MICRORNA; HYBRIDIZATION; TECHNOLOGY; PRODUCTS;
D O I
10.1039/c4ra14467h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we report a simple and homogenous fluorescence method for ultrasensitive DNA detection. It is based on rolling circle amplification (RCA) and fluorescence resonance energy transfer (FRET). As an alternative to a molecular beacon (MB), a linear single-labeled DNA probe was used in this RCA-based fluorescence strategy for DNA detection. The performance of linear DNA probes was compared with that of the MB probe in an RCA-based fluorescence strategy. The results showed that the linear DNA probes could effectively avoid the fluorescence quenching between neighboring signal probes, which would significantly improve the sensitivity of the RCA-based fluorescence strategy. This method exhibited a high sensitivity toward target DNA with a detection limit of 0.7 aM, which was about 100-fold lower than that of the RCA-based fluorescence strategy with MB as the signal probe. This method provides a simple, isothermal, and low-cost approach for sensitive detection of DNA and holds great potential for early diagnosis in gene-related diseases.
引用
收藏
页码:4019 / 4025
页数:7
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