Department of Chemistry, Sungkyunkwan University, Suwon, South Korea.
Methods Mol Biol. 2023;2651:143-155. doi: 10.1007/978-1-0716-3084-6_10.
Development of FokI-based engineered nucleases has been a platform technology that enables creation of novel sequence-specific nucleases as well as structure-specific nucleases. Z-DNA-specific nucleases have been constructed by fusing a Z-DNA-binding domain to the nuclease domain of FokI (F). In particular, Zαα, an engineered Z-DNA-binding domain with a high affinity, is an ideal fusion partner to generate a highly efficient Z-DNA-specific cutter. Here, we describe construction, expression, and purification of Zαα-FOK (Zαα-F) nuclease in detail. In addition, Z-DNA-specific cleavage is demonstrated by the use of Zαα-FOK.
基于 FokI 的工程化核酸酶的开发是一种平台技术,可用于创建新型序列特异性核酸酶和结构特异性核酸酶。通过将 Z-DNA 结合结构域融合到 FokI(F)的核酸酶结构域,构建了 Z-DNA 特异性核酸酶。特别是,具有高亲和力的工程化 Z-DNA 结合结构域 Zαα 是生成高效 Z-DNA 特异性切割酶的理想融合伴侣。在这里,我们详细描述了 Zαα-FOK(Zαα-F)核酸酶的构建、表达和纯化。此外,还通过使用 Zαα-FOK 证明了 Z-DNA 的特异性切割。