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基于 MoS/g-CN/黑 TiO 异质结的用于 microRNA 检测的光电化学生物传感器,结合 Histostar@AuNPs 用于信号放大。

Photoelectrochemical biosensor for microRNA detection based on a MoS/g-CN/black TiO heterojunction with Histostar@AuNPs for signal amplification.

机构信息

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

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

出版信息

Biosens Bioelectron. 2019 Mar 1;128:137-143. doi: 10.1016/j.bios.2018.12.048. Epub 2019 Jan 3.

DOI:10.1016/j.bios.2018.12.048
PMID:30660928
Abstract

Herein, a novel photoelectrochemical (PEC) biosensor was developed for the ultrasensitive detection of microRNA-396a based on a MoS/g-CN/black TiO heterojunction as the photoactive material and gold nanoparticles carrying Histostar antibodies (Histostar@AuNPs) for signal amplification. Briefly, MoS/g-CN/black TiO was deposited on an indium tin oxide (ITO) electrode surface, after which gold nanoparticles (AuNPs) and probe DNA were assembled on the modified electrode. Hybridization with miRNA-396a resulted in a rigid DNA: RNA hybrid being formed, which was recognized by the S9.6 antibody. The captured antibody can further conjugate with the secondary IgG antibodies of Histostar@AuNPs, thereby leading to the immobilization of horse radish peroxidase (HRP). In the presence of HRP, the oxidation of 4-chloro-1-naphthol (4-CN) by HO was accelerated, producing the insoluble product benzo-4-chlorohexadienone on the electrode surface and causing a significant decrease in the photocurrent. The developed biosensor could detect miRNA-396a at concentrations from 0.5 fM to 5000 fM, with a detection limit of 0.13 fM. Further, the proposed method can also be used to investigate the effect of heavy metal ions on the expression level of miRNAs. Results suggest that the biosensor developed herein offers a promising platform for the ultrasensitive detection of miRNA.

摘要

在此,开发了一种新型光电化学(PEC)生物传感器,用于基于 MoS/g-CN/黑 TiO 异质结作为光活性材料和携带 Histostar 抗体的金纳米粒子(Histostar@AuNPs)进行信号放大的超灵敏检测 microRNA-396a。简而言之,MoS/g-CN/黑 TiO 被沉积在铟锡氧化物(ITO)电极表面上,之后将金纳米粒子(AuNPs)和探针 DNA 组装在修饰的电极上。与 microRNA-396a 杂交导致形成刚性 DNA:RNA 杂交体,该杂交体被 S9.6 抗体识别。捕获的抗体可以进一步与 Histostar@AuNPs 的二级 IgG 抗体缀合,从而导致辣根过氧化物酶(HRP)的固定化。在 HRP 的存在下,HO 加速了 4-氯-1-萘酚(4-CN)的氧化,在电极表面上产生不溶性产物苯并-4-氯己二烯酮,导致光电流显著降低。所开发的生物传感器可以在 0.5 fM 至 5000 fM 的浓度范围内检测 microRNA-396a,检测限为 0.13 fM。此外,该方法还可用于研究重金属离子对 microRNA 表达水平的影响。结果表明,本文所开发的生物传感器为 microRNA 的超灵敏检测提供了一个有前途的平台。

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