首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Graphene oxide and gold nanoparticle based dual platform with short DNA probe for the PCR free DNA biosensing using surface-enhanced Raman scattering
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Graphene oxide and gold nanoparticle based dual platform with short DNA probe for the PCR free DNA biosensing using surface-enhanced Raman scattering

机译:石墨烯氧化物和金纳米粒子的双重平台,具有使用表面增强拉曼散射的PCR自由DNA生物溶解的短DNA探针

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摘要

Surface-enhanced Raman scattering (SERS) based DNA biosensors have considered as excellent, fast and ultrasensitive sensing technique which relies on the fingerprinting ability to produce molecule specific distinct spectra. Unlike conventional fluorescence based strategies SERS provides narrow spectral bandwidths, fluorescence quenching and multiplexing ability, and fitting attribute with short length probe DNA sequences. Herein, we report a novel and PCR free SERS based DNA detection strategy involving dual platforms and short DNA probes for the detection of endangered species, Malayan box turtle (MBT) (Cuora amboinensis). In this biosensing feature, the detection is based on the covalent linking of the two platforms involving graphene oxide-gold nanoparticles (GO-AuNPs) functionalized with capture probe 1 and gold nanoparticles (AuNPs) modified with capture probe 2 and Raman dye (Cy3) via hybridization with the corresponding target sequences. Coupling of the two platforms generates locally enhanced electromagnetic field 'hot spot', formed at the junctions and interstitial crevices of the nanostructures and consequently provide significant amplification of the SEAS signal. Therefore, employing the two SEAS active substrates and short-length probe DNA sequences, we have managed to improve the sensitivity of the biosensors to achieve a lowest limit of detection (LOD) as low as 10 fM. Furthermore, the fabricated biosensor exhibited sensitivity even for single nucleotide base-mismatch in the target DNA as well as showed excellent performance to discriminate closely related six non-target DNA sequences. Although the developed SERS biosensor would be an attractive platform for the authentication of MBT from diverse samples including forensic and/or archaeological specimens, it could have universal application for detecting gene specific biomarkers for many diseases including cancer.
机译:基于表面增强的拉曼散射(SERS)的DNA生物传感器已被认为是优异的,快速和超细感的感测技术,其依赖于产生分子特异性不同光谱的指纹识别能力。与传统的荧光基于荧光策略不同,SERS提供窄的光谱带宽,荧光猝灭和复用能力,以及具有短长探针DNA序列的拟合属性。在此,我们报告了一种基于新的和PCR自由的DNA检测策略,涉及双重平台和短DNA探针,用于检测濒危物种,Malayan Box Turtle(MBT)(Cuora amboinensis)。在这种生物传感特征中,检测基于涉及用捕获探针1和用捕获探针2和拉曼染料(Cy3)改性的捕获探针1和金纳米颗粒(AUNP)官能化的石墨烯氧化物 - 金纳米颗粒(GO-AUNP)的共价连接。通过与相应的靶序列的杂交。两个平台的耦合产生局部增强的电磁场“热点”,形成在纳米结构的结和间隙裂缝中,因此提供了大海信号的显着放大。因此,采用两个海洋活性底物和短度探针DNA序列,我们已经设法提高了生物传感器的灵敏度,以实现低至10 fm的最低检测限(LOD)。此外,制造的生物传感器即使在靶DNA中的单核苷酸碱基 - 错配,也表现出优异的性能,以区分密切相关的六种非靶DNA序列。虽然发达的SERS生物传感器是一种有吸引力的平台,用于从包括法医和/或考古标本的不同样品认证MBT的平台,但它可能具有检测基因特异性生物标志物的普遍应用,用于许多疾病,包括癌症。

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