Target-inspired Pb2+-dependent DNAzyme for ultrasensitive electrochemical sensor based on MoS2-AuPt nanocomposites and hemin/G-quadruplex DNAzyme as signal amplifier

Target-inspired Pb2+-dependent DNAzyme for ultrasensitive electrochemical sensor based on MoS2-AuPt nanocomposites and hemin/G-quadruplex DNAzyme as signal amplifier
复制标题

DOI:
10.1016/j.bios.2019.111560
复制
发表时间:
2019-11-01
影响因子:
12.6
通讯作者:
Li, Chaorui
Li, Chaorui
中科院分区:
工程技术1区
文献类型:
--
作者:
Ji, Renyue;Niu, Wuceng;Li, Chaorui

文献摘要

被引文献

相似文献

本研究利用MoS2-AuPt纳米材料和hemin/ g -四联DNAzyme作为电催化信号标签,开发了一种Pb2+电化学DNAzyme传感器,用于水环境中铅离子(Pb2+)的超灵敏检测。链霉亲和素(SA)修饰的氧化锡功能化还原氧化石墨烯(rGO-SnO2) /金纳米颗粒(AuNPs)作为传感器平台,可增强电导率并固定化更多Pb2+特异性DNAzyme。在Pb2+存在下,Pb2+依赖性DNAzyme与Pb2+特异性反应,将底物链(SS)切割成两个自由片段,并在电极上释放生物素修饰酶链(Bio-ES)。将富含G-DNA (G-DNA)链标记的MoS2-AuPt纳米复合材料与通过辅助DNA暴露的Bio-ES连接,并加入血红蛋白形成血红蛋白/ g -四重体,生物传感器实现了信号放大。电流信号主要来自于MoS2-AuPt纳米复合材料和血红素/ g四联体对H2O2的共催化还原。在最佳条件下,所设计的生物传感器对Pb2+的检测灵敏度在0.1 pg mL(-1)至1000 ng mL(-1)之间,最低检测限为38 fg mL(-1)(基于3 σ)。该生物传感器具有超灵敏和特异性,代表了水环境中Pb2+检测的潜在应用。
In this work, a novel Pb2+ electrochemical DNAzyme sensor was developed for ultrasensitive detection of lead ions (Pb2+) in water environment by coupling with the MoS2-AuPt nanomaterials and hemin/G-quadruplex DNAzyme, which acting as the electrocatalytic signal tag. Streptavidin (SA) modified tin dioxide-functionalized reduced graphene oxide (rGO-SnO2) /gold nanoparticles (AuNPs) served as a sensor platform for enhancing conductivity and immobilizing more Pb2+-specific DNAzyme. In the presence of Pb2+, the Pb2+-dependent DNAzyme specifically reacted with Pb2+, cleaving the substrate strand (SS) into two free fragment and releasing the biotin-modified enzyme strand (Bio-ES) on the electrode. Connecting MoS2-AuPt nanocomposites labeled with G-rich DNA (G-DNA) strand and exposure of Bio-ES through the Helper DNA, as well as adding hemin to form a hemin/G-quadruplex, the biosensor achieved signal amplification. Chronoamperometry was used to record the current signal, which was primarily derived from the cocatalysis reduction of H2O2 by MoS2-AuPt nanocomposites and the hemin/G-quadruplex. Under optimal conditions, the designed biosensor exhibited sensitive detection of Pb2+ from 0.1 pg mL(-1) to 1000 ng mL(-1), with a lower detection limit of 38 fg mL(-1) (based on 3 sigma). This proposed biosensor is ultrasensitive and specific, representing a potential application for the detection of Pb2+ in a water environment.