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Toehold-mediated strand displacement coupled with single nanoparticle dark-field microscopy imaging for ultrasensitive biosensing

机译:再加上Toehold-mediated链位移单一纳米粒子暗视野显微镜成像对超灵敏的若

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摘要

Highly sensitive detection of biomarkers is essential for disease prevention and early diagnosis. Herein, a highly sensitive strategy was proposed for microRNA-21 (miRNA-21) detection by the incorporation of programmable toehold-mediated strand displacement (TMSD) and dark-field microscopy imaging. Firstly, efficient and specific TSMD was carried out via hybridization between the substrate strand (Sub) and two short probe strands (P1, P2). Then, miRNA-21 could specifically hybridize with Sub due to the toehold that existed on its tail, which triggered the amplification with the help of the assist strands, and forming a large number of Sub-assist double-stranded DNA (dsDNA). This process realized the targeted highly specific recognition of miRNA-21 and the amplification of the trace target to high-output dsDNA. Additionally, as glucose oxidase (Gox) was modified on the end of the assist strands in advance, hydrogen peroxide was generated after adding glucose to the system, which further etched gold–silver core–shell nanocubes (Au@Ag NCs). As a result, the size of Au@Ag NCs decreased and the scattering intensity reduced simultaneously. The scattering intensity reduction value of Au@Ag NCs has a linear relationship with miRNA-21 concentration in the range of 1.0 to 100.0 fM with a limit of detection of 1.0 fM. Finally, the proposed method has been successfully demonstrated for the determination of miRNA-21 in lung cancer cell A549 lysate.
机译:高度敏感的生物标志物的检测疾病预防和早期的必要条件诊断提出了对microRNA-21 (miRNA-21)检测公司的可编程toehold-mediated链位移(TMSD)和暗视野显微镜成像。和具体TSMD通过底物链之间的杂交(子)和两个探针短链(P1, P2)。miRNA-21可以专门杂交子由于存在于它的尾巴的立足之地,引发了放大的帮助吗协助链,形成大量Sub-assist双链DNA (dsDNA)。过程实现了非常具体的目标承认miRNA-21和放大高通量dsDNA跟踪目标。此外,葡萄糖氧化酶(气态氧)协助链的最后修改进步,过氧化氢生成葡萄糖添加到系统nc)。减少和散射强度降低同时进行。减少的价值Au@Ag nc线性与miRNA-21浓度之间的关系1.0到100.0调频范围的限制1.0 fM的检测。已经成功了的测定miRNA-21在肺癌细胞A549溶解产物。

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