摘要
为研究重组腺病毒载体作为HPV16预防性疫苗的可行性,构建了含密码子优化型HPV 16 L1基因的重组腺病毒,并对优化基因在哺乳动物细胞中的表达进行研究。首先按照哺乳动物密码子偏好对野生型HPV16 L1基因进行改造并合成优化基因,命名为mod.HPV16L1。将mod.HPV16L1基因克隆到穿梭质粒PDC316上,与骨架质粒共转染293细胞,在细胞内包装重组腺病毒rAd-mod.HPV16L1。用免疫印迹法检测病毒感染的293T细胞中HPV16L1蛋白的表达。通过Optiprep密度梯度超速离心法纯化HPV16 L1病毒样颗粒(VLPs)。用磷钨酸负染,在电子显微镜下观察HPV16 L1蛋白自我装配形成的VLPs。结果显示,重组腺病毒载体可介导mod.HPV16 L1基因在哺乳动物细胞内的高效表达,L1蛋白可自我装配形成VLPs。
To investigate the feasibility of using recombinant adenovirus vector as prophylactic vaccine against HPV infection, a recombinant adenovirus containing codon modified HPV16 L1 gene was constructed, and the expression of the optimized gene in mammalian cells mediated by adenovirus was evaluated, We optimized the codon usage of wild type HPV 16 L1 gene according to the codon bias of mammalian, and synthesized the fulllength optimized L1 gene, named mod. HPV16L1, which was later cloned to shuttle plasmid PDC316,and cotransfected with the backbone plasmid into 293 cell for tAd production. We detected the expression of HPV16 L1 protein in tAd infected 293T cell by Western blot, and purified the HPV16 virus-like particles that self-assembled in 293T cell using Optiprep density gradient ultracentrifugation. The purified HPV16 L1 virus-like particles were seen under the electron microscope. The results showed the recombinant adenovirus, rAdmod. HPV16L1, mediated highly efficient expression of codon-modified HPV16L1 gene in mammalian cell. The L1 protein could self-assemble into VLPs in mammalian cell.
出处
《病毒学报》
CAS
CSCD
北大核心
2006年第2期101-106,共6页
Chinese Journal of Virology
基金
国家高技术"863"计划资助项目(2001AA215221)
国家"973"资助项目(2004C9818806)
关键词
腺病毒
人乳头瘤病毒16型
密码子优化
病毒样颗粒
adenovirus
human papillomavirus 16
codon modification
virus-like particles（VLPs）
