通过荧光和 SERS 分子信标联合测定法检测人类病毒 RNA。

M Y Sha, S Penn, G Freeman, W E Doering
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引用次数: 0

摘要

我们开发了一种复用基底上的双模式分子信标,并将其应用于测量未标记的人类病毒 RNA。该检测系统基于组装在 Nanobarcodes™ 颗粒上的表面增强拉曼散射(SERS)和荧光分子信标检测组合。在这种检测方法中,以荧光拉曼标签染料为终端的分子信标探针被连接到金属 Nanobarcodes™ 颗粒上。分子信标探针是一种单链寡核苷酸,设计有发夹结构,当探针通过 5'-thiol 基团连接时,可将染料固定在靠近颗粒表面的 3'端。在这种结构中,由于染料非常接近具有纳米级特征的贵金属表面(Nanobarcodes™ 颗粒),因此可以获得标签的 SERS 光谱并淬灭其荧光。当目标病毒 RNA 被这种分子信标探针捕获时,SERS 信号减弱,荧光信号增强。此外,还利用这种双模式信标检测到了丙型肝炎病毒逆转录酶聚合酶链反应(HCV RT-PCR)产物。开发出一种复用、无标记的检测系统,并通过检测两种截然不同的信号提供保证,为快速分子诊断带来了巨大的好处。
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Detection of human viral RNA via a combined fluorescence and SERS molecular beacon assay.

A dual-mode molecular beacon on a multiplexed substrate has been developed and applied to the measurement of unlabeled human viral RNA. The detection system is based on a combined surface-enhanced Raman scattering (SERS) and fluorescent molecular beacon assay that is assembled on Nanobarcodes™ particles. In this assay, a molecular beacon probe terminated with a fluorescent Raman label dye is conjugated to the metallic Nanobarcodes™ particles. The molecular beacon probe is a single-stranded oligonucleotide that has been designed with a hairpin structure that holds the dye at 3'-end close to the particle surface when the probe is attached through a 5'-thiol group. In this configuration, the SERS spectrum of the label was obtained and its fluorescence quenched because the dye is in very close proximity to a noble metal surface with nanoscale features (Nanobarcodes™ particles). The SERS signal decreased and the fluorescence signal increased when target viral RNA was captured by this molecular beacon probe. In addition, a hepatitis C virus reverse transcriptase-polymerase chain reaction (HCV RT-PCR) product was detected using this dual-mode beacon. The development of a multiplexed, label-free assay system with the reassurance offered by detection of two distinctly separate signals offers significant benefits for rapid molecular diagnostics.

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