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Detection of Hepatitis B Virus M204I Mutation by Quantum Dot-Labeled DNA Probe

机译:量子点标记DNA探针检测乙型肝炎病毒M204I突变

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摘要

Quantum dots (QDs) are semiconductor nanoparticles with a diameter of less than 10 nm, which have been widely used as fluorescent probes in biochemical analysis and vivo imaging because of their excellent optical properties. Sensitive and convenient detection of hepatitis B virus (HBV) gene mutations is important in clinical diagnosis. Therefore, we developed a sensitive, low-cost and convenient QDs-mediated fluorescent method for the detection of HBV gene mutations in real serum samples from chronic hepatitis B (CHB) patients who had received lamivudine or telbivudine antiviral therapy. We also evaluated the efficiency of this method for the detection of drug-resistant mutations compared with direct sequencing. In CHB, HBV DNA from the serum samples of patients with poor response or virological breakthrough can be hybridized to probes containing the M204I mutation to visualize fluorescence under fluorescence microscopy, where fluorescence intensity is related to the virus load, in our method. At present, the limits of the method used to detect HBV genetic variations by fluorescence quantum dots is 10 3 IU/mL. These results show that QDs can be used as fluorescent probes to detect viral HBV DNA polymerase gene variation, and is a simple readout system without complex and expensive instruments, which provides an attractive platform for the detection of HBV M204I mutation.
机译:量子点(QD)是直径小于10 nm的半导体纳米粒子,由于其出色的光学性能,已广泛用作生化分析和体内成像的荧光探针。灵敏且方便地检测乙型肝炎病毒(HBV)基因突变在临床诊断中很重要。因此,我们开发了一种灵敏,低成本且方便的QDs介导的荧光方法,用于检测接受拉米夫定或替比夫定抗病毒治疗的慢性乙型肝炎(CHB)患者的真实血清样本中的HBV基因突变。与直接测序相比,我们还评估了该方法检测耐药突变的效率。在CHB中,我们的方法可以将来自反应较差或病毒学突破患者血清样本中的HBV DNA与含有M204I突变的探针杂交,以在荧光显微镜下观察荧光,其中荧光强度与病毒载量有关。目前,用于通过荧光量子点检测HBV遗传变异的方法的限制为10 3 IU / mL。这些结果表明,量子点可以用作检测病毒HBV DNA聚合酶基因变异的荧光探针,并且是一种简单的读出系统,无需复杂且昂贵的仪器,这为检测HBV M204I突变提供了一个有吸引力的平台。

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