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氧化石墨烯修饰铅笔石墨电极用于DNA杂交的无电化学标记灵敏纳米生物传感

Electrochemical label-free and sensitive nanobiosensing of DNA hybridization by graphene oxide modified pencil graphite electrode.

作者信息

Ahour F, Shamsi A

机构信息

Nanotechnology Research Center, Faculty of Science, Urmia University, Urmia, Iran.

Nanotechnology Research Center, Faculty of Science, Urmia University, Urmia, Iran.

出版信息

Anal Biochem. 2017 Sep 1;532:64-71. doi: 10.1016/j.ab.2017.06.004. Epub 2017 Jun 9.

DOI:10.1016/j.ab.2017.06.004
PMID:28606426
Abstract

Based on the strong interaction between single-stranded DNA (ss-DNA) and graphene material, we have constructed a novel label-free electrochemical biosensor for rapid and facile detection of short sequences ss-DNA molecules related to hepatitis C virus 1a using graphene oxide modified pencil graphite electrode. The sensing mechanism is based on the superior adsorption of single-stranded DNA to GO over double stranded DNA (ds-DNA). The intrinsic guanine oxidation signal measured by differential pulse voltammetry (DPV) has been used for duplex DNA formation detection. The probe ss-DNA adsorbs onto the surface of GO via the π- π* stacking interactions leading to a strong background guanine oxidation signal. In the presence of complementary target, formation of helix which has weak binding ability to GO induced ds-DNA to release from the electrode surface and significant variation in differential pulse voltammetric response of guanine bases. The results indicated that the oxidation peak current was proportional to the concentration of complementary strand in the range of 0.1 nM-0.5 μM with a detection limit of 4.3 × 10 M. The simple fabricated electrochemical biosensor has high sensitivity, good selectivity, and could be applied as a new platform for a range of target molecules in future.

摘要

基于单链DNA(ss-DNA)与石墨烯材料之间的强相互作用,我们使用氧化石墨烯修饰的铅笔石墨电极构建了一种新型的无标记电化学生物传感器,用于快速简便地检测与丙型肝炎病毒1a相关的短序列ss-DNA分子。传感机制基于单链DNA对氧化石墨烯的吸附优于双链DNA(ds-DNA)。通过差分脉冲伏安法(DPV)测量的鸟嘌呤固有氧化信号已用于双链DNA形成检测。探针ss-DNA通过π-π*堆积相互作用吸附在氧化石墨烯表面,导致强烈的背景鸟嘌呤氧化信号。在存在互补靶标的情况下,与氧化石墨烯结合能力较弱的螺旋结构的形成会诱导ds-DNA从电极表面释放,并导致鸟嘌呤碱基的差分脉冲伏安响应发生显著变化。结果表明,氧化峰电流在0.1 nM至0.5 μM范围内与互补链浓度成正比,检测限为4.3×10 M。这种简单制备的电化学生物传感器具有高灵敏度、良好的选择性,未来可作为一系列靶标分子的新平台。

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