Ultrasensitive and rapid detection of miRNA with three-way junction structure-based trigger-assisted exponential enzymatic amplification

被引:44
|
作者
Xu, Ying [1 ]
Wang, Yu [1 ]
Liu, Su [3 ]
Yu, Jinghua [2 ]
Wang, Hongzhi [2 ]
Guo, Yuna [2 ]
Huang, Jiadong [1 ,2 ]
机构
[1] Univ Jinan, Coll Biol Sci & Technol, Key Lab Chem Sensing & Anal Univ Shandong, Jinan 250022, Peoples R China
[2] Univ Jinan, Coll Chem & Chem Engn, Jinan 250022, Peoples R China
[3] Univ Jinan, Coll Resources & Environm, Jinan 250022, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Three-way junction structure; EXPAR; Isothermal synergetic enzyme amplification; miRNA detection; QUADRATIC ISOTHERMAL AMPLIFICATION; ROLLING CIRCLE AMPLIFICATION; HIGHLY SENSITIVE DETECTION; RECYCLING AMPLIFICATION; STACKING HYBRIDIZATION; MICRORNA DETECTION; CANCER; DNA; LEVEL; STRATEGY;
D O I
10.1016/j.bios.2016.02.034
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Aberrant expression of micro RNA (miRNA) is associated with development of cancers and diseases, so miRNA has become a tissue-based biomarker for cancer prognosis and diagnosis. Herein, a novel trigger assisted exponential enzymatic amplification (T-EXPEA) method for ultrasensitive miRNA detection based on three-way junction (3-WJ) structure driven has been reported, which can be used in potential applications in cancer prognosis and diagnoses. In this assay, target miRNA can unfold hairpin probe and start the reaction, and thus specifically form stable 3-WJ structure with helper. Then it can produce triggers under the synergetic polymerase and restriction endonucleases amplification. The produced triggers could be used to unfold molecular beacon (MB) and initiate T-EXPEA process. In the EXPEA part, the exponential triggers were generated to initiate new T-EXPEA and high enhancement fluorescence amplification efficiency was obtained. The feature of our strategy lies in the T-EXPEA combining with 3-WJ structure has been utilized for fluorescence miRNA detection. It is worth noting that the sequence of the triggers in T-EXPEA part is the same to that of triggers generated from the 3-WJ part. In addition, the design of restriction enzyme cutting sites using the same restriction enzyme (Nt.BbvCI) in hairpin probe and MB respectively, improved reaction efficiency cost-efficiently. This method can quantitatively detect sequence-specific miRNA in a dynamic range from 10 aM to 10 pM with a detection limit as low as 7.8 aM. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 241
页数:6
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