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大肠杆菌来源的人乳头瘤病毒11型病毒样颗粒的制备及其免疫原性
引用本文:杨春燕,李少伟,王晋,魏旻希,黄博,庄玉娣,李仲艺,潘晖榕,张军?,夏宁邵.大肠杆菌来源的人乳头瘤病毒11型病毒样颗粒的制备及其免疫原性[J].微生物学报,2009,49(11):1527-1533.
作者姓名:杨春燕  李少伟  王晋  魏旻希  黄博  庄玉娣  李仲艺  潘晖榕  张军?  夏宁邵
作者单位:厦门大学生命科学学院,国家传染病诊断试剂与疫苗工程技术研究中心,细胞生物学与肿瘤细胞工程教育部重点实验室,厦门,361005
基金项目:基金项目:国家“863计划”——国家高技术研究发展计划重点项目(2006AA020905);国家自然科学基金(30500092);科技部工程中心建设项目(2005DC105006);教育部新世纪优秀人才培养计划(NCET-05-0567)
摘    要:摘要:【目的】 利用大肠杆菌表达系统制备人乳头瘤病毒11型病毒样颗粒(HPV11 VLPs),并对其免疫原性和所诱导中和抗体的型交叉反应性进行研究。 【方法】 在大肠杆菌ER2566中非融合表达HPV11-L1蛋白,并通过离子交换层析,疏水相互作用层析其进行纯化。纯化后的HPV11-L1经体外组装形成病毒样颗粒,通过动态光散射,透射电镜检测其形态,并通过多种HPV型别假病毒中和实验评价HPV11 VLPs的免疫原性及型交叉反应性。 【结果】 HPV11-L1蛋白在大肠杆菌中可以以可溶形式表达。经过硫酸铵沉

关 键 词:关键词:  人乳头瘤病毒11型    大肠杆菌表达系统    病毒样颗粒    免疫原性    型交叉中和
收稿时间:2009/4/13 0:00:00
修稿时间:2009/6/11 0:00:00

Expression, purification and immunogenicity of human papillomavirus type 11 virus-like particles from Escherichia coli
Chunyan Yang,Shaowei Li,Jin Wang,Minxi Wei,Bo Huang,Yudi Zhuang,Zhongyi Li,Huirong Pan,Jun Zhang? and Ningshao Xia.Expression, purification and immunogenicity of human papillomavirus type 11 virus-like particles from Escherichia coli[J].Acta Microbiologica Sinica,2009,49(11):1527-1533.
Authors:Chunyan Yang  Shaowei Li  Jin Wang  Minxi Wei  Bo Huang  Yudi Zhuang  Zhongyi Li  Huirong Pan  Jun Zhang? and Ningshao Xia
Institution:National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China;National Institute of Diagnostics and Vaccine Development in infectious diseases, Life Science School, Key Laboratory of the Ministry of Education for Cell Biology and Tumor Cell Engineering, Xiamen University, Xiamen 361005, China
Abstract:Objective] To produce human papillomavirus type 11 virus-like particles (HPV11 VLPs) from Escherichia coli and to investigate its immunogenicity and type cross neutralization nature. Methods] We expressed the major capsid protein of HPV11 (HPV11-L1) in Escherichia coli ER2566 in non fusion fashion and purified by amino sulfate precipitation, ion-exchange chromatography and hydrephobic interaction chromatography, sequentially. Then we removed the reductant DTT to have the purified HPV11-L1 self-assemble into VLPs in vitro. We investigated the morphology of these VLPs with dynamic light scattering and transmission electron microscopy. We assayed the immunogenicity of the resultant HPV11 VLPs by vaccinations on mice and evaluated by HPV6/11/16/18 pseudovirion neutralization cell models. Results] We expressed HPV11 L1 in Escherichia coli with two forms, soluble and inclusion body. The soluble HPV11 L1 with over 95% purity can self assemble to VLPs in high efficiency. Morphologically, these VLPs were globular, homogeneous and with a diameter of~50 nm, which is quite similar with native HPV11 virious. The half effective dosage (ED_(50)) of HPV11 VLPs is 0.031 μg, and the maximum titer of neutralizing antibody elicited is averaged to 10~6. The cross neutralization activity (against HPV6/16/18) of the anti-HPV11 serum was found to have exact correlation to the inter-type homology in amino acid alignment. Conclusion] We can provide HPV11 VLPs with highly immunogenicity from prokaryote expression system, which may pave a new way for research and development of prophylactic vaccine for HPV11.
Keywords:Keywords: human papillomavirus type 11  Escherichia coli  virus-like particle  immunogenicity  cross neutralization
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