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Development of a nanoparticle-based electrochemical bio-barcode DNA biosensor for multiplexed pathogen detection on screen-printed carbon electrodes.

机译:基于纳米粒子的电化学生物条形码DNA生物传感器的开发,用于在丝网印刷的碳电极上进行多重病原体检测。

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摘要

A highly amplified, nanoparticle-based, bio-barcoded electrochemical biosensor for the simultaneous multiplexed detection of the protective antigen A (pagA) gene (accession number = M22589) from Bacillus anthracis and the insertion element (Iel) gene (accession number = Z83734) from Salmonella Enteritidis was developed. The biosensor system is mainly composed of three nanoparticles: gold nanoparticles (AuNPs), magnetic nanoparticles (MNPs), and nanoparticle tracers (NTs), such as lead sulfide (PbS) and cadmium sulfide (CdS). The AuNPs are coated with the first target-specific DNA probe (1pDNA), which can recognize one end of the target DNA sequence (tDNA), and many NT-terminated bio-barcode ssDNA (bDNA-NT), which act as signal reporter and amplifier. The MNPs are coated with the second target-specific DNA probe (2pDNA) that can recognize the other end of the target gene. After binding the nanoparticles with the target DNA, the following sandwich structure is formed: MNP-2pDNA/tDNA/1pDNA-AuNP-bDNA-NTs. A magnetic field is applied to separate the sandwich structure from the unreacted materials. Because the AuNPs have a large number of nanoparticle tracers per DNA probe binding event, there is substantial amplification. After the nanoparticle tracer is dissolved in 1 mol/L nitric acid, the NT ions, such as Pb 2+ and Cd2+, show distinct non-overlapping stripping curves by square wave anodic stripping voltammetry (SWASV) on screen-printed carbon electrode (SPCE) chips. The oxidation potential of NT ions is unique for each nanoparticle tracer and the peak current is related to the target DNA concentration. The results show that the biosensor has good specificity, and the sensitivity of single detection of pagA gene from Bacillus anthracis using PbS NTs is as low as 0.2 pg/mL. The detection limit of this multiplex bio-barcoded DNA sensor is 50 pg/mL using PbS or CdS NTs. The nanoparticle-based bio-barcoded DNA sensor has potential applications for multiple detections of bioterrorism threat agents, co-infection, and contaminants in the same sample.
机译:一种高度放大的,基于纳米粒子的生物条形码电化学生物传感器,用于同时多重检测炭疽芽孢杆菌的保护性抗原A(pagA)基因(登录号= M22589)和插入元件(Iel)基因(登录号= Z83734)由肠炎沙门氏菌研制而成。生物传感器系统主要由三个纳米粒子组成:金纳米粒子(AuNPs),磁性纳米粒子(MNPs)和纳米粒子示踪剂(NTs),例如硫化铅(PbS)和硫化镉(CdS)。 AuNP被第一个靶标特异性DNA探针(1pDNA)包裹,该探针可以识别靶标DNA序列(tDNA)的一端,还有许多NT端接的生物条形码ssDNA(bDNA-NT),它们可以充当信号报告基因和放大器。 MNP涂有可以识别靶基因另一端的第二个靶特异性DNA探针(2pDNA)。将纳米粒子与目标DNA结合后,形成以下夹心结构:MNP-2pDNA / tDNA / 1pDNA-AuNP-bDNA-NTs。施加磁场以将夹层结构与未反应的材料分离。因为每个DNA探针结合事件AuNPs都有大量的纳米粒子示踪剂,所以存在大量的扩增。将纳米颗粒示踪剂溶于1 mol / L硝酸中后,通过丝网印刷碳电极(SPCE)上的方波阳极溶出伏安法(SWASV),NT离子(例如Pb 2+和Cd2 +)显示出明显的非重叠溶出曲线)筹码。 NT离子的氧化势对于每个纳米粒子示踪剂而言都是唯一的,并且峰值电流与目标DNA浓度有关。结果表明,该生物传感器具有良好的特异性,使用PbS NTs对炭疽芽孢杆菌单次检测pagA基因的灵敏度低至0.2 pg / mL。使用PbS或CdS NTs,该多重生物条形码DNA传感器的检测极限为50 pg / mL。基于纳米粒子的生物条形码DNA传感器具有潜在用途,可用于对同一样品中的生物恐怖威胁因子,共感染和污染物进行多次检测。

著录项

  • 作者

    Zhang, Deng.;

  • 作者单位

    Michigan State University.;

  • 授予单位 Michigan State University.;
  • 学科 Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 108 p.
  • 总页数 108
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:45:14

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