【摘要】 目的对构建重组腺病毒的AdEasy载体系统的操作过程予以改进,使其更加简便、高效。方法将腺病毒骨架载体pAdEasy-1用电穿孔法转化大肠埃希菌BJ5183,获得含pAdEasy-1的大肠埃希菌BJ5183/p菌株。氯化钙法制备大肠埃希菌BJ5183/p感受态细胞,并转化含绿色荧光蛋白的穿梭载体,通过同源重组获得重组腺病毒质粒。以限制性内切酶PacⅠ酶切,得到重组腺病毒DNA分子,转染293细胞。结果293细胞出现细胞病变,荧光显微镜观察有绿色荧光。结论成功获得一种以AdEasy系统为基础的简便、高效构建重组腺病毒的新方法。更多还原

【Abstract】 Objective To Obtain a more effective and easier method for constructing recombinant adenovirus by simplifying the protocol of the AdEasy system.Methods The replication-defective adenovirus type 5 backbone plasmid pAdEasy-1 was transformed into competent E.coli BJ5183 by electroporation and the E.coli BJ5183/p was obtained. Then E.coli BJ5183/p competent cells were prepared by CaCl₂ technique and the shuttle plasmid carrying green fluorescent protein （GFP） was transformed into E.coli BJ5183.The confirmed recombinant was linearlized with Pac I and transfected into 293 cell line.Results The CPE of 293 cells were observed and the green fluorescence was seen under fluorescent microscope.Conclusion A more effective and easier method for constructing recombinant adenovirus based on AdEasy was obtained successfully.更多还原