Digital CRISPR-based quantification of HIV-1

Reza Nouri, Yuqian Jiang, Anthony J. Politza, Xiaojun Lian, W. Guan
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Abstract

Here, we demonstrate a membrane-based digital CRISPR-Cas13a system for amplification-free absolute quantification of viral particles of HIV-1. We established a stamping technique to digitalize the Cas13 assay inside a commercial track-etched polycarbonate (PCTE) membrane. We evaluated the performance of our system by quantifying the synthetic HIV-1 RNA, where a limit of detection of 100 aM was achieved in 30 min reaction. Absolute quantification of the viral particles HIV-1 in plasma background using our system confirmed that our system can quantify spiked samples.
基于数字crispr的HIV-1定量
在这里,我们展示了一种基于膜的数字CRISPR-Cas13a系统,用于HIV-1病毒颗粒的无扩增绝对定量。我们建立了一种冲压技术来数字化Cas13测定在商业轨迹蚀刻聚碳酸酯(PCTE)膜内。我们通过定量合成HIV-1 RNA来评估系统的性能,在30分钟的反应中达到了100 aM的检测限。使用我们的系统对血浆背景中HIV-1病毒颗粒的绝对定量证实了我们的系统可以定量加标样品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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