首页> 外文会议>The 1st International Conference on Bioinformatics and Biomedical Engineering(iCBBE 2007) >Combining Gold Nanoparticles with Real-Time Immuno-PCR for Analysis of HIV p24 Antigens
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Combining Gold Nanoparticles with Real-Time Immuno-PCR for Analysis of HIV p24 Antigens

机译:结合金纳米粒子与实时免疫PCR分析HIV p24抗原

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We have improved real-time immuno-PCR (IPCR) with nanoparticle based amplification. Gold magnetic particles were functionalized with antibodies against the HIV capsid protein p24 and gold nanoparticles were functionalized with both oligonucleotide barcodes and antibodies against a nonoverlapping region of the cognate p24. In the presence of p24, the gold magnetic particles and the gold nanoparticles form sandwiched structures that are magnetically separated from mixture. After dehybridization of the barcode DNA on the gold nanoparticle, the released barcodes are quickly identified by realtime PCR. The limit of detection was 100 copies of p24 antigens.Results show that the real-time IPCR through nanoparticle based barcode amplification offers an disruptive approach to p24 detection and quantification, thus may potentially shorten the window of HIV-1 diagnosis, and might be valuable to monitor the response to anti-retroviral treatment when RNA copy number is very below.
机译:我们已经改进了基于纳米粒子的实时免疫PCR(IPCR)。金磁性颗粒用抗HIV衣壳蛋白p24的抗体功能化,金纳米颗粒用寡核苷酸条形码和抗同源p24的非重叠区域的抗体功能化。在存在p24的情况下,金磁性颗粒和金纳米颗粒形成从混合物中磁性分离的夹心结构。在金纳米颗粒上的条形码DNA脱杂交后,通过实时PCR快速识别释放的条形码。检测极限是100份p24抗原。结果表明,基于纳米颗粒的条形码扩增的实时IPCR提供了一种破坏性的p24检测和定量方法,因此可能会缩短HIV-1诊断的时间,可能具有重要的价值。监测RNA拷贝数非常低时对抗逆转录病毒治疗的反应。

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