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Single-Walled Carbon Nanotubes as Enhancing Substrates for PNA-Based Amperometric Genosensors

机译:单壁碳纳米管作为基于PNA的电流型基因传感器的增强基质

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摘要

A new amperometric sandwich-format genosensor has been implemented on single-walled carbon nanotubes screen printed electrodes (SWCNT-SPEs) and compared in terms of performance with analogous genoassays developed using the same methodology on non-nanostructured glassy carbon platforms (GC-SPE). The working principle of the genosensors is based on the covalent immobilization of Peptide Nucleic Acid (PNA) capture probes (CP) on the electrode surface, carried out through the carboxylic functions present on SWCNT-SPEs (carboxylated SWCNT) or electrochemically induced on GC-SPEs. The sequence of the CP was complementary to a 20-mer portion of the target DNA; a second biotin-tagged PNA signalling probe (SP), with sequence complementary to a different contiguous portion of the target DNA, was used to obtain a sandwich hybrid with an Alkaline Phosphatase-streptavidin conjugate (ALP-Strp). Comparison of the responses obtained from the SWCNT-SPEs with those produced from the non-nanostructured substrates evidenced the remarkable enhancement effect given by the nanostructured electrode platforms, achieved both in terms of loading capability of PNA probes and amplification of the electron transfer phenomena exploited for the signal transduction, giving rise to more than four-fold higher sensitivity when using SWCNT-SPEs. The nanostructured substrate allowed to reach limit of detection (LOD) of 71 pM and limit of quantitation (LOQ) of 256 pM, while the corresponding values obtained with GC-SPEs were 430 pM and 1.43 nM, respectively.
机译:已在单壁碳纳米管丝网印刷电极(SWCNT-SPE)上实现了一种新的安培型三明治格式基因传感器,并与在非纳米结构玻碳平台(GC-SPE)上使用相同方法开发的类似基因分析方法进行了性能比较。 。遗传传感器的工作原理基于将肽核酸(PNA)捕获探针(CP)共价固定在电极表面上,通过SWCNT-SPEs(羧基化SWCNT)上存在的羧基功能或在GC- SPE。 CP的序列与靶DNA的20聚体部分互补。第二个生物素标记的PNA信号探针(SP)具有与目标DNA的不同连续部分互补的序列,被用来获得带有碱性磷酸酶-链霉亲和素偶联物(ALP-Strp)的三明治杂交体。通过比较SWCNT-SPEs和非纳米结构基底产生的响应,可以看出纳米结构电极平台具有显着的增强作用,无论是在PNA探针的负载能力还是在电子探针的放大方面都可以实现。信号转导,使用SWCNT-SPE时灵敏度提高了四倍以上。纳米结构的底物允许达到71 pM的检出限(LOD)和256 pM的定量限(LOQ),而用GC-SPEs获得的相应值分别为430 pM和1.43 nM。

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