荧光
纳米团簇
滚动圆复制
化学
纳米传感器
互补DNA
DNA
检出限
小RNA
生物物理学
纳米技术
生物化学
基因
材料科学
色谱法
生物
物理
DNA复制
有机化学
量子力学
作者
Zhanmin Liu,Yanming Wang,Junhai Li,Yuanyuan Yuan,Xianyong Wu,Wenruo Liu,Youwei Liu
标识
DOI:10.1016/j.aca.2019.08.052
摘要
For early detection and diagnosis of gastric cancer, a novel, highly sensitive detection of microRNA-378 was developed through rolling circle amplification and DNA-templated silver nanoclusters as a lable-free fluorescent probe. DNA-templated fluorescent silver nanoclusters (DNA/AgNCs) to make target signal cascade amplification were prepared and identified through their fluorescent spectrum. MiRNA-378 trigged rolling circle amplification to obtain the complementary sequence (cDNA) to combine with two DNA/AgNCs in the middle of a sandwich structure to induce the new fluorescent signal at a new wavelength. In the presence of microRNA-378, a large amount of RCA product cDNAs were hybridized with DNA/AgNCs as the fluorescence nanocluster beacon, resulting in fluorescence enhanced "turn-on" phenomenon. This study indicated that amplified fluorescence detection of microRNA-378 is a stable, low-cost, highly specific, and ultra-low as 1.07 fM detectability. The proposed approach of signal synergetic amplification facilitating the fluorescence detection microRNA shows great potential for potentially clinically diagnosis.
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