Hairpin DNA-Templated Silver Nanoclusters as Novel Beacons in Strand Displacement Amplification for MicroRNA Detection

被引:104
作者
Zhang, Jingpu [1 ,2 ]
Li, Chao [1 ]
Zhi, Xiao [2 ]
Ramon, Gabriel Alfranca [1 ]
Liu, Yanlei [1 ,2 ]
Zhang, Chunlei [1 ]
Pan, Fei [1 ,3 ]
Cui, Daxiang [1 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Inst Nano Biomed & Engn, Key Lab Thin Film & Microfabricat, Minist Educ,Dept Instrument Sci & Engn,Sch Elect, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Biomed Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Natl Ctr Translat Med, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
关键词
ISOTHERMAL AMPLIFICATION; CIRCULAR-DICHROISM; FLUORESCENT; PROBE;
D O I
10.1021/acs.analchem.5b03729
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
MicroRNA (miRNA) biomarkers display great potential for cancer diagnosis and prognosis. The development of rapid and specific methods for miRNA detection has become a hotspot. Herein, hairpin DNA-templated silver nanoclusters (AgNCs/HpDNA) were prepared and integrated into strand-displacement amplification (SDA) as a novel beacon for miRNA detection. The light-up platform was established based on guanine (G)-rich fluorescence enhancement that essentially converted the excitation/emission pair of AgNCs/HpDNAs from a shorter wavelength to a longer wavelength, and then achieved fluorescent enhancement at longer wavelength. On the basis of the validation of the method, the single and duplex detection were conducted in two plasma biomarkers (miR-16-5p and miR-19b-3p) for the diagnosis of gastric cancer. The probe (AgNCs/RED 16(7s)C) utilized for miR-16-5p detection adopted a better conformation with high specificity to recognize single-base mismatches by producing dramatically opposite signals (increase or decrease at 580 nm ex/640 nm em) while the probe (AgNCs/GRE 19b(5s)C) for miR-19b-3p generated dual signals (increase at 490 nm ex/570 nm em and decrease at 430 nm ex/530 nm em) with bright fluorescence in one reaction during the amplification, but unexpectedly was partially digested. This is for the first time to allow the generation of enhanced fluorescent AgNCs and the target recognition integrated into a single process, which offers great opportunity for specific miRNA detection in an easy and rapid way.
引用
收藏
页码:1294 / 1302
页数:9
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