Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.
Department of Biology, Faculty of Sciences, Shahid Bahonar University of Kerman, Kerman, Iran.
Biosens Bioelectron. 2020 Dec 15;170:112710. doi: 10.1016/j.bios.2020.112710. Epub 2020 Oct 8.
In recent years, DNA logic gates have been extensively applied in developing multiplex processing platforms to provide an accurate decision on the diagnosis of multi-factor diseases. In this work, we presented a new cascaded logical operator by combining different modules for computational monitoring of four miRNAs related to Alzheimer disease (has-miR-143-3p, has-miR-18b-5p, has-miR-424-5p, and has-miR-93-5p). Herein, three sequential logic gates were programed that upon entering the miRNA inputs, delivered the trigger strand of CHA (catalytic hairpin assembly) reaction through a cyclic amplification. Afterward, the product of the CHA reaction, three-way junction, could induce the gold nanoparticles aggregation. This phenomenon led to generate a blue color of the solution that enabled visualizing and quantitative measurement of the assay. The output signals were recorded through reading the absorbance intensity transition, dynamic light scattering (DLS), and transmission electron microscopy (TEM). Taken together, the proposed assay by taking advantage of excellent generality, naked eye observation, the 4-plex detection, simplicity, enzyme-free nature, and two-steps process without any immobilization and washing has addressed the limitation of the previous systems. Moreover, the amplified monitoring of low-abundant of target miRNAs was accomplished with a limit of detection as low as 5 pM.
近年来,DNA 逻辑门已广泛应用于开发多重处理平台,以对多因素疾病的诊断做出准确决策。在这项工作中,我们通过组合不同的模块,提出了一种新的级联逻辑运算符,用于计算监测与阿尔茨海默病相关的四种 miRNA(has-miR-143-3p、has-miR-18b-5p、has-miR-424-5p 和 has-miR-93-5p)。在此,我们设计了三个顺序逻辑门,当输入 miRNA 时,通过循环扩增将 CHA(催化发夹组装)反应的触发链传递出去。之后,CHA 反应的产物三链结能够诱导金纳米粒子聚集。这种现象导致溶液呈现蓝色,从而可以可视化和定量测量该测定。通过读取吸光度强度转换、动态光散射 (DLS) 和透射电子显微镜 (TEM) 来记录输出信号。总之,该测定法利用了优异的通用性、肉眼观察、4 重检测、简单性、无酶特性以及两步过程(无需任何固定化和洗涤),解决了先前系统的局限性。此外,通过低至 5 pM 的检测限实现了对低丰度靶标 miRNA 的放大监测。