Self-driven and self-catalytic tripedal DNA nanomachine for rapid and sensitive detection of miR-21 in in colorectal cancer.

Qin Ma, Yilong Tu, Wen Yun, Mingming Zhang
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Abstract

A self-driven and self-catalytic (SDSC) tripedal DNA nanomachine was developed for microRNA-21 (miR-21) detection. The microRNA could open one arm of tripedal DNA nanomachine to form DNAzyme with a nearby arm through the proximity effect. After DNAzyme's cleavage, the exposed DNA arm region competed with the third arm and produced a DNA segment (sequence Q). The released sequence Q initiated the next SDSC cycle of tripedal DNA nanomachine. In the special DNA nanomachines design, the components with close spatial localization were constructed on a single nanostructure, which significantly increased local reactant concentrations and reaction rates. A dynamic correlation was obtained from 10 pM to 50 nM between fluorescence signal and miR-21 concentration. The effective concentration of reactant greatly increased, compared with the free diffusible reactants. Consequently, the incubation time was significantly shorted to 35 min. This strategy showed a promising potential in miRNA detection and disease diagnosis.

自驱动自催化三足DNA纳米机用于快速灵敏检测结直肠癌中miR-21 in。
开发了一种自驱动自催化(SDSC)三足DNA纳米机,用于检测microRNA-21 (miR-21)。通过接近效应,microRNA可以打开三足DNA纳米机器的一只手臂,与另一只手臂形成DNAzyme。DNAzyme切割后,暴露的DNA臂区与第三臂区竞争,产生一个DNA片段(序列Q)。释放的序列Q启动了下一个三足DNA纳米机器的SDSC循环。在特殊的DNA纳米机器设计中,将空间定位紧密的组分构建在单个纳米结构上,显著提高了局部反应物浓度和反应速率。从10 pM到50 nM荧光信号与miR-21浓度呈动态相关。与自由扩散反应物相比,反应物的有效浓度大大提高。因此,孵育时间显著缩短至35分钟。该策略在miRNA检测和疾病诊断方面显示出良好的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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