Huang Weiwei, Zhao Xiangqian, Zheng Chunfu, Shen Yangkun
Department of Medical Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
The Cancer Center, Union Hospital, Fujian Medical University, Fuzhou, China.
Methods Mol Biol. 2025;2940:109-119. doi: 10.1007/978-1-0716-4615-1_10.
CRISPR-mediated gene knock-in is a powerful tool for studying virus-host interactions. In this protocol, we describe the methodology for the knock-in of a red fluorescent protein, mCherry, fused to the viral protein VP26, a component of the herpesvirus capsid. By integrating the mCherry gene into the HSV-1 genome, we enable detailed studies of viral protein dynamics, viral replication, and virus-host interactions in living cells. In particular, this approach allows real-time monitoring of the subcellular localization of the viral capsid. The protocol provides a step-by-step guide for designing the gene knock-in vectors, transfection, selection, and validation of the mCherry fusion to the VP26 protein in the HSV-1 genome.
CRISPR介导的基因敲入是研究病毒-宿主相互作用的强大工具。在本方案中,我们描述了将红色荧光蛋白mCherry与病毒蛋白VP26(疱疹病毒衣壳的一个组成部分)融合进行敲入的方法。通过将mCherry基因整合到单纯疱疹病毒1型(HSV-1)基因组中,我们能够在活细胞中详细研究病毒蛋白动力学、病毒复制以及病毒-宿主相互作用。特别地,这种方法允许实时监测病毒衣壳的亚细胞定位。该方案为设计基因敲入载体、转染、筛选以及验证HSV-1基因组中mCherry与VP26蛋白的融合提供了详细的步骤指南。