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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Dual catalytic DNA circuit-induced gold nanoparticle aggregation: An enzyme-free and colorimetric strategy for amplified detection of nucleic acids
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Dual catalytic DNA circuit-induced gold nanoparticle aggregation: An enzyme-free and colorimetric strategy for amplified detection of nucleic acids

机译:双催化DNA电路诱导的金纳米颗粒聚集:一种无菌和比色策略,用于扩增核酸的检测

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摘要

An enzyme-free dual catalytic DNA circuit for amplified detection of nucleic acids has been developed. The system functions based on a cyclic self-assembly of two auxiliary hairpins (H1 and H2) and three biotinylated hairpin oligonucleotides (H3, H4 and H5), in the format of two molecular circuits. In the upstream circuit, a target initiator (I) besides H1 and H2 hairpins constructs H1-H2 duplexes that trigger the operation of a subsequent circuit. In the downstream circuit, the H1-H2 duplex initiates cascaded self-assembly reactions, produces triplex H3-H4-H5, as sensing system, and releases the H1-H2 duplex as the catalyst for the self-assembly of additional hairpins. The H3-H4-H5 triplex acts as the scaffolds for assembling and orienting the streptavidin-functionalized gold nanoparticles (SA-AuNPs) into a lattice-like arrangement that generates a DNA-SA-AuNP cross-linked network, resulting in a dramatic pale red-to-blue color change. By ingeniously engaging two catalytic circuits with feedback amplification capabilities, the system can detect the target nucleic acid with an LOD value of 5 femtomolar and unambiguously discriminate spurious targets (i.e. targets containing substitution, insertion, and deletion nucleotides) without instrumentation. Simple and convenient operation of the assay makes the DNA circuit appropriate for point-of-care monitoring in resource-constrained settings. (C) 2020 Published by Elsevier B.V.
机译:已经开发出用于扩增核酸检测的一种无酶双催化DNA电路。基于两个辅助发夹(H1和H2)的循环自组装和三种生物素化的发夹寡核苷酸(H3,H4和H5)的循环自组装,以两个分子回路的形式。在上游电路中,除了H1和H2发夹之外的目标引发剂(I)构建触发后续电路的操作的H1-H2双工。在下游电路中,H1-H2双相发起级联的自组装反应,产生三重单反滑的H3-H4-H5,作为传感系统,并将H1-H2双链体释放为额外发夹的自组装的催化剂。 H3-H4-H5 Triplex作为用于组装和定向链霉抗生物素蛋白官能化的金纳米颗粒(SA-AUNP)的支架,以晶格状的布置,其产生DNA-SA-AUNP交联网络,导致剧烈的苍白红蓝色变化。通过巧妙地与反馈扩增能力接合两个催化电路,系统可以检测靶核酸,含有5毫托麦柯尔的洛氏菌素,并明确区分杂散靶标(即含有替代,插入和缺失核苷酸的靶标)而没有仪器。测定的简单和方便的操作使DNA电路适用于资源受限设置中的护理点监测。 (c)2020由elsevier b.v发布。

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