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首页> 外文期刊>AIDS Research and Human Retroviruses >Novel Time-Resolved Fluorescence Europium Nanoparticle Immunoassay for Detection of Human Immunodeficiency Virus-1 Group O Viruses Using Microplate and Microchip Platforms
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Novel Time-Resolved Fluorescence Europium Nanoparticle Immunoassay for Detection of Human Immunodeficiency Virus-1 Group O Viruses Using Microplate and Microchip Platforms

机译:使用微孔板和微芯片平台的新型时间分辨荧光Euro纳米粒子免疫测定法,用于检测人类免疫缺陷病毒-1组O病毒。

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摘要

Accurate detection and quantification of HIV-1 group O viruses have been challenging for currently available HIV assays. We have developed a novel time-resolved fluorescence (TRF) europium nanoparticle immunoassay for HIV-1 group O detection using a conventional microplate enzyme-linked immunosorbent assay (ELISA) and a microchip platform. We screened several antibodies for optimal reactivity with several HIV-1 group O strains and identified antibodies that can detect all the strains of HIV-1 group O that were available for testing. The antibodies were used to develop a conventional ELISA format assay and an in-house developed europium nanoparticle-based assay for sensitivity. The method was evaluated on both microwell plate and microchip platforms. We identified two specific and sensitive antibodies among the six we screened. The antibodies, C65691 and ANT-152, were able to quantify 15 and detect all 17 group O viruses, respectively, as they were broadly cross-reactive with all HIV-1 group O strains and yielded better signals compared with other antibodies. We have developed a sensitive assay that reflects the actual viral load in group O samples by using an appropriate combination of p24 antibodies that enhance group O detection and a highly sensitive TRF-based europium nanoparticle for detection. The combination of ANT-152 and C65690M in the ratio 3:1 was able to give significantly higher signals in our europium-based assay compared with using any single antibody.
机译:对HIV-1 O组病毒的准确检测和定量对于当前可用的HIV检测方法一直具有挑战性。我们开发了一种新型的时间分辨荧光(TRF)nano纳米粒子免疫测定法,用于使用常规微孔板酶联免疫吸附测定法(ELISA)和微芯片平台检测HIV-1组O。我们筛选了几种与几种HIV-1 O型毒株最佳反应的抗体,并鉴定了可以检测所有可用于测试的HIV-1 O型毒株的抗体。抗体用于开发常规ELISA格式测定法和内部开发的基于euro纳米粒子的灵敏度测定法。该方法在微孔板和微芯片平台上进行了评估。我们在筛选的六种抗体中鉴定出两种特异性和敏感性抗体。抗体C65691和ANT-152能够分别定量15种病毒和检测所有17种O型病毒,因为它们与所有HIV-1 O型毒株具有广泛的交叉反应性,并且比其他抗体产生更好的信号。我们已经开发出一种灵敏的检测方法,它可以通过使用适当的增强O组检测的p24抗体和高度敏感的基于TRF的euro纳米颗粒进行组合来反映O组样品中的实际病毒载量。与使用任何单一抗体相比,ANT-152和C65690M的比例为3:1的组合能够在我们基于assay的测定中给出明显更高的信号。

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