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CRISPR-Cas9 vectors for genome editing and host engineering in the baculovirus–insect cell system

机译:杆状病毒-昆虫细胞系统中用于基因组编辑和宿主工程的CRISPR-Cas9载体

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摘要

The baculovirus–insect cell system (BICS) has been widely used to produce many different recombinant proteins for basic research and is being used to produce several biologics approved for use in human or veterinary medicine. Early BICS were technically complex and constrained by the relatively primordial nature of insect cell protein glycosylation pathways. Since then, recombination has been used to modify baculovirus vectors—which has simplified the system—and transform insect cells, which has enhanced its protein glycosylation capabilities. Now, CRISPR-Cas9 tools for site-specific genome editing are needed to facilitate further improvements in the BICS. Thus, in this study, we used various insect U6 promoters to construct CRISPR-Cas9 vectors and assessed their utility for site-specific genome editing in two insect cell lines commonly used as hosts in the BICS. We demonstrate the use of CRISPR-Cas9 to edit an endogenous insect cell gene and alter protein glycosylation in the BICS.
机译:杆状病毒-昆虫细胞系统(BICS)已被广泛用于生产许多用于基础研究的重组蛋白,并且已被用于生产批准用于人类或兽医学的多种生物制剂。早期的BICS在技术上很复杂,并且受到昆虫细胞蛋白糖基化途径相对原始的限制。从那时起,重组已被用于修饰杆状病毒载体(简化了系统)并转化昆虫细胞,从而增强了其蛋白质糖基化能力。现在,需要用于特定位点基因组编辑的CRISPR-Cas9工具,以促进BICS的进一步改进。因此,在这项研究中,我们使用了多种昆虫U6启动子构建CRISPR-Cas9载体,并评估了它们在BICS中通常用作宿主的两种昆虫细胞系中进行位点特异性基因组编辑的效用。我们证明了使用CRISPR-Cas9编辑内源性昆虫细胞基因并改变BICS中的蛋白质糖基化。

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