首页 | 本学科首页   官方微博 | 高级检索  
检索        

昆虫细胞偏爱密码子优化的HPV16L1基因在昆虫和哺乳动物细胞中的表达
引用本文:宋敬东,王健伟,王敏,郭丽,屈建国,鲁茁壮,韩金祥,洪涛.昆虫细胞偏爱密码子优化的HPV16L1基因在昆虫和哺乳动物细胞中的表达[J].中国病原生物学杂志,2007,2(4):247-251.
作者姓名:宋敬东  王健伟  王敏  郭丽  屈建国  鲁茁壮  韩金祥  洪涛
作者单位:1. 山东省病毒学研究所暨山东省医学病毒学重点实验室/卫生部生物技术药物重点实验室/山东省现代医用药物与技术重点实验室,山东济南,250062;中国疾病预防控制中心病毒病预防控制所,北京,100052
2. 山东省病毒学研究所暨山东省医学病毒学重点实验室/卫生部生物技术药物重点实验室/山东省现代医用药物与技术重点实验室,山东济南,250062;中国医学科学院病原生物学研究所,北京,100730
3. 中国疾病预防控制中心病毒病预防控制所,北京,100052
4. 山东省病毒学研究所暨山东省医学病毒学重点实验室/卫生部生物技术药物重点实验室/山东省现代医用药物与技术重点实验室,山东济南,250062
5. 山东省病毒学研究所暨山东省医学病毒学重点实验室/卫生部生物技术药物重点实验室/山东省现代医用药物与技术重点实验室,山东济南,250062;中国疾病预防控制中心病毒病预防控制所,北京,100052;中国医学科学院病原生物学研究所,北京,100730
摘    要:目的获得有效表达人乳头瘤病毒16型(HPV16)L1基因的重组杆状病毒和腺病毒,为研究HPV的免疫保护机制提供材料。方法按照昆虫细胞密码子偏爱优化并合成HPV16LI基因,利用Bac—to-Bac昆虫表达系统获得表达HPV16L1基因的重组杆状病毒,利用AdEasy腺病毒载体系统获得表达HPV16L1基因的重组腺病毒载体。通过间接免疫荧光和Westernblot对HPV16L1基因表达进行鉴定,利用负染电子显微镜观察病毒样颗粒(VLP)的形成。结果获得了稳定表达HPV16L1蛋白的重组杆状病毒和重组腺病毒载体,在Sf9细胞和293细胞中可有效表达能被抗HPV16L1单克隆抗体识别的L1蛋白,分子质量单位为56ku,在Sf9细胞中可观察到VLP的形成。结论按照昆虫细胞密码子偏爱进行优化的HPV16L1基因,在昆虫细胞和哺乳动物细胞内均可有效表达。

关 键 词:人乳头瘤病毒L1  16型  重组腺病毒  重组杆状病毒  表达  密码子优化  病毒样颗粒
文章编号:1673-5234(2007)04-0247-05
收稿时间:2006-12-20
修稿时间:2006-12-202007-03-13

The optimization of human papillomavirus type 16L1 gene following the insect cell condon bias can achieve effective expression in both insect and mammalian cells
SONG Jing-dong,WANG Jian-wei,WANG Min,GUO Li,QU Jian-guo,LU Zhuo-zhuang,HAN Jin-xiang,HONG Tao.The optimization of human papillomavirus type 16L1 gene following the insect cell condon bias can achieve effective expression in both insect and mammalian cells[J].Journal of Pathogen Biology,2007,2(4):247-251.
Authors:SONG Jing-dong  WANG Jian-wei  WANG Min  GUO Li  QU Jian-guo  LU Zhuo-zhuang  HAN Jin-xiang  HONG Tao
Institution:1. Shandong Provincial Institute of Virology/ Shandong Provincial Key Laboratory of Medical Virology and Key Laboratory of Biotechnological Pharmaceuticals, Ministry of Health, China/ Key Laboratory for Modern Medicine and Technology of Shandong Province, Jinan 250062, Chinas2. National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 100052, China; 3. Institute of Pathogen Biology, Chinese Academy of Medical Sciences, Beijing 100730, China
Abstract:Objective To generate recombinant baculovirus and adenovirus which can express human papillomavirus type 16(HPV16) L1 gene to provide materials for investigating the immunological mechanisms of HPV infection.Methods The HPV16L1 gene was artificially synthesized after optimization following insect cell codon bias.The recombinant baculovirus and adenovirus harboring the HPV16L1 were generated through Bac-to-Bac Baculovirus Expression System and AdEasy Adenoviral Vector System,respectively.The expression of the HPV16L1 was confirmed by both indirect immunofluorescence and Western blot.The virus-like particles(VLPs) of HPV16 was identified by negative staining electron microscopy.Results Both the recombinant baculovirus and adenovirus bearing HPV16L1 were successfully generated.The effective expression of HPV16L1 in insect Sf9 cells or 293 cells were detected by the monoclonal antibody which is specific to HPV16 L1,respectively,and the assembly of VLPs was observed in Sf9 cells.Conclusion The HPV16L1 gene optimized according to insect cell condon bias can be expressed effectively in both insect and mammalion cells.
Keywords:Human papillomavirus type 16 L1  recombinant adenovirus  recombinant baculovirus  expression  codon optimization  virus-like particle(VLP)
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号