Plasmon Coupling-Enhanced Raman Sensing Platform Integrated with Exonuclease-Assisted Target Recycling Amplification for Ultrasensitive and Selective Detection of microRNA-21

被引:60
|
作者
Wen, Shengping [1 ,3 ]
Su, Yu [1 ]
Dai, Chuanxiang [1 ,4 ]
Jia, Junran [1 ]
Fan, Gao-Chao [2 ]
Jiang, Li-Ping [1 ]
Song, Rong-Bin [1 ]
Zhu, Jun-Jie [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Jiangsu, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Shandong Key Lab Biochem Anal, Key Lab Opt Elect Sensing & Analyt Chem Life Sci, Qingdao 266042, Shandong, Peoples R China
[3] Guangdong Pharmaceut Univ, Sch Chinese Med Resources, Yunfu 527300, Guangdong, Peoples R China
[4] Nanjing Univ, Coll Engn & Appl Sci, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
SIGNAL AMPLIFICATION; FLUORESCENCE DETECTION; GOLD NANOSTARS; NANOPARTICLES; SCATTERING; BIOSENSOR; STRATEGY; SPECTROSCOPY; PROBES;
D O I
10.1021/acs.analchem.9b02476
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A "signal-off' surface-enhanced Raman scattering (SERS) platform has been constructed for ultrasensitive detection of miRNA-21 by integrating exonuclease-assisted target recycling amplification with a plasmon coupling enhancement effect. On this platform, Raman-labeled Au nanostar (AuNS) probes can be covalently linked with the thiolated aptamer (Apt) on the Au-decorated silicon nanowire arrays (SiNWAs/Au) substrate, creating a coupled electromagnetic field between the substrate and the probes to enhance Raman signal. In the presence of miRNA-21, T7 exonuclease specifically hydrolyzed Apt on Apt/miRNA duplex to release miRNA-21. The regenerated element could then initiate another cycle of Apt/miRNA duplex formation and Apt cleavage. Correspondingly, the capture ability of substrate toward probes and the plasmon coupling effect between them were both diminished, giving a prominent attenuation of Raman intensity that can work as the detection signal. Due to the cascading integration between the target cycle process and the plasmon coupling effect, the present platform displayed a very low detection limit (0.34 fM, 3 sigma) for miRNA-21 detection. Furthermore, it was proven to be effective for analyzing miRNA-21 in biological samples and distinguishing the expression levels of miRNA-21 in MCF-7 cells and NIH3T3 cells, which became a promising tool to monitor miRNA-21 in cancer auxiliary diagnosis and drug screening.
引用
收藏
页码:12298 / 12306
页数:9
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