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一种基于血红素/石墨烯@钯铂纳米粒子的新型双信号无标记电化学粘蛋白1适配体传感器。

A novel dual signal and label-free electrochemical aptasensor for mucin 1 based on hemin/graphene@PdPtNPs.

作者信息

Zhang Guojuan, Liu Zhiguang, Fan Lifang, Han Yujie, Guo Yujing

机构信息

Institute of Environmental Science, Shanxi University, Taiyuan, 030006, China.

Institute of Environmental Science, Shanxi University, Taiyuan, 030006, China.

出版信息

Biosens Bioelectron. 2021 Feb 1;173:112785. doi: 10.1016/j.bios.2020.112785. Epub 2020 Nov 4.

Abstract

A dual signal and label-free electrochemical aptasensor for mucin 1 was constructed based on hemin/graphene@PdPtNPs nanocomposite (H-Gr@PdPtNPs). Hemin attached on the graphene surface not only improves the solubility of graphene and acts as an in-situ electrochemical probe but also exhibits excellent peroxidase-like properties to electrocatalyze the reduction of HO. PdPtNPs also show outstanding catalytic capacity to the reduction of HO and provide numerous binding sites for loading dDNA (mucin 1 aptamer and cDNA) to form the sensing interface. In the presence of mucin 1, due to the specific affinity between aptamer and mucin 1, double helix would be induced dissociation and the aptamer would be pulled off from the electrode. As a result, the electrochemical signals of hemin and HO were recovered. Based on these properties, the label-free and sensitive dual signal electrochemical biosensor for mucin 1 detection has been developed. The one is differential pulse voltammetry (DPV) signal of hemin and the other is chronoamperometry signal arisen from the catalytic reduction of HO. The linear ranges for mucin 1 were 8.0 pg mL to 80 ng mL and 0.8 pg mL to 80 ng mL with the limit of detection 2.5 pg mL and 0.25 pg mL by DPV and chronoamperometry, respectively. The recovery of mucin 1 in human blood serum samples was from 95.0% to 104.2%. The detection platform does not need signal labeling which greatly reduced the sophisticated and expensive procedures. The aptasensor provide a promising strategy for the determination of mucin 1 in clinical diagnostics.

摘要

基于血红素/石墨烯@钯铂纳米粒子(H-Gr@PdPtNPs)构建了一种用于检测粘蛋白1的双信号、无标记电化学适体传感器。附着在石墨烯表面的血红素不仅提高了石墨烯的溶解度并作为原位电化学探针,还表现出优异的过氧化物酶样性质,可电催化过氧化氢的还原。钯铂纳米粒子对过氧化氢的还原也具有出色的催化能力,并为加载双链DNA(粘蛋白1适配体和互补DNA)提供大量结合位点以形成传感界面。在存在粘蛋白1的情况下,由于适配体与粘蛋白1之间的特异性亲和力,双链螺旋会被诱导解离,适配体将从电极上脱落。结果,血红素和过氧化氢的电化学信号得以恢复。基于这些特性,开发了用于检测粘蛋白1的无标记、灵敏的双信号电化学生物传感器。一个是血红素的差分脉冲伏安法(DPV)信号,另一个是由过氧化氢催化还原产生的计时电流法信号。粘蛋白1的线性范围分别为8.0 pg mL至80 ng mL(DPV法)和0.8 pg mL至80 ng mL(计时电流法),检测限分别为2.5 pg mL和0.25 pg mL。人血清样本中粘蛋白1的回收率为95.0%至104.2%。该检测平台无需信号标记,大大减少了复杂且昂贵的程序。该适体传感器为临床诊断中粘蛋白1的测定提供了一种有前景的策略。

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