College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, China.
School of Chemistry and Environmental Engineering, Pingdingshan University, Pingdingshan 467000, China.
Biosensors (Basel). 2023 Jun 30;13(7):699. doi: 10.3390/bios13070699.
The double specific nuclease (DSN)-based methods for microRNAs (miRNAs) detection usually require the immobilization of DNA probes on a solid surface. However, such strategies have the drawbacks of low hybridization and cleavage efficiency caused by steric hindrance effect and high salt concentration on the solid surface. Herein, we proposed an immobilization-free method for miRNA detection on the basic of DSN-assisted signal amplification. The biotin- and fluorophore-labeled probes were captured by streptavidin-modified magnetic beads through streptavidin-biotin interactions, thus producing a poor fluorescence signal. Once the DNA probes were hybridized with target miRNA in solution to form DNA-miRNA duplexes, DNA stands in the duplexes would be selectively digested by DSN. The released target miRNA could initiate the next hybridization/cleavage recycling in the homogeneous solution, finally resulting in the release of numerous fluorophore-labeled fragments. The released fluorophores remained in solution and emitted strong fluorescence after treatment by the streptavidin-modified magnetic beads. The immobilization-free method achieved the assays of miRNA-21 with a detection limit down to 0.01 pM. It was employed to evaluate the expression levels of miRNA-21 in different cancer cells with satisfactory results.
基于双特异性核酸酶 (DSN) 的 microRNAs (miRNAs) 检测方法通常需要将 DNA 探针固定在固体表面上。然而,这种策略存在由于固体表面上的空间位阻效应和高盐浓度导致杂交和切割效率低的缺点。在此,我们提出了一种基于 DSN 辅助信号放大的 miRNA 无固定化检测方法。生物素和荧光标记的探针通过链霉亲和素-生物素相互作用被链霉亲和素修饰的磁性珠捕获,从而产生较差的荧光信号。一旦 DNA 探针在溶液中与靶 miRNA 杂交形成 DNA-miRNA 双链体,双链体中的 DNA 链就会被 DSN 选择性地消化。释放的靶 miRNA 可以在均相溶液中引发下一次杂交/切割循环,最终导致大量荧光标记片段的释放。释放的荧光体在经过链霉亲和素修饰的磁性珠处理后仍留在溶液中并发出强荧光。无固定化方法实现了 miRNA-21 的测定,检测限低至 0.01 pM。它被用于评估不同癌细胞中 miRNA-21 的表达水平,结果令人满意。