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基于石墨烯、锁核酸整合分子信标、金纳米粒子和生物素多功能生物条码以及酶联检测系统的 microRNA-21 的电化学测定。

Electrochemical determination of microRNA-21 based on graphene, LNA integrated molecular beacon, AuNPs and biotin multifunctional bio bar codes and enzymatic assay system.

机构信息

College of Chemistry and Material Science, Shandong Agricultural University, Taian, 271018, Shandong, China.

出版信息

Biosens Bioelectron. 2012 Mar 15;33(1):247-53. doi: 10.1016/j.bios.2012.01.014. Epub 2012 Jan 23.

Abstract

MicroRNAs (miRNAs), a kind of small, endogenous, noncoding RNAs (∼22 nucleotides), might play a crucial role in early cancer diagnose due to its abnormal expression in many solid tumors. As a result, label-free and PCR-amplification-free assay for miRNAs is of great significance. In this work, a highly sensitive biosensor for sequence specific miRNA-21 detection without miRNA-21 labeling and enrichment was constructed based on the substrate electrode of dendritic gold nanostructure (DenAu) and graphene nanosheets modified glassy carbon electrode. Sulfydryl functionalized locked nucleic acid (LNA) integrated hairpin molecule beacon (MB) probe was used as miRNA-21 capture probe. After hybridized with miRNA-21 and reported DNA loading in gold nanoparticles (AuNPs) and biotin multi-functionalized bio bar codes, streptavidin-HRP was brought to the electrode through the specific interaction with biotin to catalyze the chemical oxidation of hydroquinone by H(2)O(2) to form benzoquinone. The electrochemical reduction signal of benzoquinone was utilized to monitor the miRNA-21 hybridization event. The effect of experimental variables on the amperometric response was investigated and optimized. Based on the specific confirmation of probe and signal amplification, the biosensor showed excellent selectivity and high sensitivity with low detection limit of 0.06 pM. Successful attempts are made in miRNA-21 expression analysis of human hepatocarcinoma BEL-7402 cells and normal human hepatic L02 cells.

摘要

微小 RNA(miRNAs)是一种小型、内源性、非编码 RNA(约 22 个核苷酸),由于其在许多实体瘤中的异常表达,可能在早期癌症诊断中发挥重要作用。因此,miRNAs 的无标记和无 PCR 扩增检测具有重要意义。在这项工作中,构建了一种基于树枝状金纳米结构(DenAu)和石墨烯纳米片修饰玻碳电极的底物电极的高度灵敏的miRNA-21 序列特异性检测生物传感器,用于检测miRNA-21,无需对 miRNA-21 进行标记和富集。巯基化锁定核酸(LNA)整合发夹分子信标(MB)探针用作 miRNA-21 捕获探针。与 miRNA-21 杂交后,报告 DNA 加载到金纳米粒子(AuNPs)和生物素多功能生物条码中,链霉亲和素-HRP 通过与生物素的特异性相互作用被带到电极上,以催化 H2O2 对氢醌的化学氧化,形成苯醌。利用苯醌的电化学还原信号来监测 miRNA-21 杂交事件。研究并优化了实验变量对电流响应的影响。基于探针的特异性确认和信号放大,该生物传感器表现出优异的选择性和高灵敏度,检测限低至 0.06 pM。成功尝试了人肝癌 BEL-7402 细胞和正常人肝 L02 细胞中 miRNA-21 表达的分析。

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