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3D DNA nanonet structure coupled with target -catalyzed hairpin assembly for dual -signal synergistically ampli fi ed electrochemical sensing of circulating microRNA

机译:3D DNA纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米纳米型发夹组件用于双重协同的循环微罗纳的协同电化学传感

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摘要

DNA nanomaterials are reliable and powerful tools in the development of a variety of biosensors owing to their notable self-assembly ability and precise recognition capability. Here, we propose a DNA nanomaterial-based system for the dual-amplified electrochemical sensing of circulating microRNAs by a coupled cascade of catalyzed hairpin assembly (CHA) and three-dimensional (3D) DNA nanonet structure. In the target-assisted CHA process, the stable hairpin structures H1 and H2 act as probes for the recognition and recycling of circulating microRNAs, leading to the formation of abundant H1H2 duplexes with tails. Subsequently, a 3D DNA nanonet structure was introduced, which was assembled using three DNA strands constructed X-DNA monomers as the building blocks, and hybridized to the tails of H1H2 duplexes. The successful integration of target-assisted CHA and 3D DNA nanonet structure induced the second signal amplification. The designed biosensor performed under optimized experimental conditions, and exposed admirable analytical performance for the detection of circulating miR-21, with a wide linear range from 10 fM to 1 nM, high sensitivity of limit of detection (LOD) of 3.6083 fM, good specificity in the face of single nucleotides and other microRNAs, satisfactory stability and reproducibility for practical analysis. Furthermore, the clinical applicability for circulating miR-21 detection was verified in human serum samples without additional treatment. We hope that this elaborated biosensor will provide new opportunities for bioassays based on DNA nanomaterials.
机译:由于其显着的自组装能力和精确的识别能力,DNA纳米材料在开发各种生物传感器方面是可靠和强大的工具。这里,通过催化的发夹组件(CHA)和三维(3D)DNA纳米纳米纳米结构的耦合级联,提出了一种用于双扩增的微小RNA的DNA纳米材料系统。在目标辅助的CHA工艺中,稳定的发夹结构H1和H2充当循环微小RNA的识别和再循环的探针,导致具有尾部的丰富的H1H2双链体。随后,引入了3D DNA纳米纳米结构,其使用三种DNA链组装为构建的X-DNA单体作为建筑物,并与H1H2双工的尾部杂交。目标辅助CHA和3D DNA纳米纳米键结构的成功集成诱导第二信号放大。设计的生物传感器在优化的实验条件下进行,并且对循环miR-​​21检测的暴露令人允许的分析性能,宽线性范围为10 fm至1nm,检测极限的高灵敏度(lod)为3.6083 fm,特异性良好面对单一核苷酸和其他微大罗氏,令人满意的稳定性和实际分析的再现性。此外,在人血清样品中验证了循环miR-​​21检测的临床适用性,无需额外处理。我们希望这家精心调整的生物传感器将为基于DNA纳米材料提供新的生物测量机会。

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