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基于多功能磁性纳米粒子探针与杂交链式反应偶联的 microRNAs 同时电化学检测

Simultaneously electrochemical detection of microRNAs based on multifunctional magnetic nanoparticles probe coupling with hybridization chain reaction.

机构信息

College of Chemistry and Institute for Advanced Study, Nanchang University, Nanchang 330031, China.

College of Chemistry and Institute for Advanced Study, Nanchang University, Nanchang 330031, China.

出版信息

Biosens Bioelectron. 2017 Nov 15;97:325-331. doi: 10.1016/j.bios.2017.06.022. Epub 2017 Jun 11.

DOI:10.1016/j.bios.2017.06.022
PMID:28622643
Abstract

We report a sensor combining two distinguishable magnetic nanoprobes (DNA1/FeO NPs/Thi and DNA2/FeO NPs/Fc) with target-triggered hybridization chain reaction (HCR) strategy for the simultaneous detection of microRNA-141 (miR-141) and microRNA-21 (miR-21). In the presence of targets, the thiol-modified hairpin capture probes (HCP1 and HCP2) specifically hybridize with miR-141 and miR-21 on a gold electrode, leading to the conformation change of HCP1 and HCP2, respectively. The conformation change subsequently triggers HCR to generate plentiful bonding sequences of magnetic nanoprobes. Thus, numerous thionine (Thi) modified DNA1/FeO NPs/Thi and ferrocene carboxaldehyde (Fc-CHO) modified DNA2/FeO NPs/Fc are captured by the well-designed HCR, via DNA hybridization respectively, giving rise to the dual magnified response of currents. The increase in the electrochemical currents at different potentials of the two magnetic nanoprobes enables us to simultaneously and quantitatively detect miR-141 and miR-21. Target-triggered HCR increases the amount of captured nanoprobes due to the increasing number of bonding sequences, greatly amplifying the currents of the two magnetic nanoprobes in the presence of targets, and ultimately realizing the dual signal amplification with increased sensitivity. The sensor can be applied for detecting miRNAs in cell lysates, thus, promising to be a clinic diagnosis of cancers by means of simultaneous detection of a variety of miRNA biomarkers.

摘要

我们报告了一种传感器,该传感器结合了两种可区分的磁性纳米探针(DNA1/FeO NPs/Thi 和 DNA2/FeO NPs/Fc)与基于目标触发的杂交链式反应(HCR)策略,用于同时检测 microRNA-141(miR-141)和 microRNA-21(miR-21)。在存在靶标的情况下,巯基修饰的发夹捕获探针(HCP1 和 HCP2)特异性地与金电极上的 miR-141 和 miR-21 杂交,分别导致 HCP1 和 HCP2 的构象变化。构象变化随后触发 HCR 生成大量磁性纳米探针的结合序列。因此,通过 DNA 杂交,大量的硫堇(Thi)修饰的 DNA1/FeO NPs/Thi 和二茂铁甲醛(Fc-CHO)修饰的 DNA2/FeO NPs/Fc 被精心设计的 HCR 捕获,从而导致电流的双重放大响应。两种磁性纳米探针在不同电位下的电化学电流的增加使得我们能够同时和定量地检测 miR-141 和 miR-21。由于结合序列的数量增加,目标触发的 HCR 增加了捕获的纳米探针的数量,大大放大了存在靶标时两种磁性纳米探针的电流,最终实现了具有更高灵敏度的双信号放大。该传感器可用于检测细胞裂解物中的 miRNAs,因此有望通过同时检测多种 miRNA 生物标志物实现癌症的临床诊断。

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