State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences , Wuhan, P.R. China.
Beijing Key Laboratory of Bioprocess, College of Life Science and Technology, Beijing University of Chemical Technology , Beijing, P.R. China.
Anal Chem. 2017 Dec 5;89(23):12896-12901. doi: 10.1021/acs.analchem.7b03584. Epub 2017 Nov 21.
HIV latency is one of the major problems in HIV/AIDS cure. Imaging single-copy integrated proviral HIV DNA in host cell has both virology and clinical significance but remains technical challenge. Here, we developed a dual-color labeled CRISPR system to image the HIV-1 integrated proviral DNA in latently infected cells. The pair of CRISPRs was fluorescently labeled with two different color QDs using two alternative bioorthogonal ligation reactions. Integrated HIV-sequences are successfully mapped based on the colocalized signals of QDs in living cells. Compared to the existing zinc finger proteins and TALENs, the CRISPR system is much easier to operate and more efficient in imaging of internal genomic loci. Therefore, the proposed method could be not only a powerful tool for imaging proviral HIV-1, but also a versatile platform to image single genomic loci in living cells.
HIV 潜伏期是 HIV/AIDS 治疗中的主要问题之一。对宿主细胞中单拷贝整合前病毒 HIV DNA 的成像具有病毒学和临床意义,但仍然存在技术挑战。在这里,我们开发了一种双色标记的 CRISPR 系统来对潜伏感染细胞中的 HIV-1 整合前病毒 DNA 进行成像。这对 CRISPR 通过两种替代的生物正交连接反应用两种不同颜色的 QD 进行荧光标记。基于活细胞中 QD 的共定位信号,成功地对整合的 HIV 序列进行了作图。与现有的锌指蛋白和 TALENs 相比,CRISPR 系统在内部基因组位点成像方面操作更简单,效率更高。因此,该方法不仅可以成为一种对 HIV-1 前病毒成像的强大工具,还可以作为一种在活细胞中对单个基因组位点成像的通用平台。