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密码子优化型HPV16L1基因在两种昆虫细胞中的表达

Expression of Codon-optimized Human Papillomavirus 16 L1 Gene in Two Insect Cells
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摘要 目的:提高16型人乳头瘤病毒(HPV16)L1基因在杆状病毒昆虫细胞中的表达水平,为研制预防性HPV疫苗奠定基础。方法:根据昆虫细胞密码子偏性对野生型HPV16L1基因进行改造,利用Bac-to-Bac表达系统获得重组杆状病毒,感染昆虫细胞Sf9和High Five。Western blot鉴定表达产物;电镜下观察病毒样颗粒形成。利用ELISA法评价HPV16L1基因的优化效果,探讨L1蛋白表达的最佳条件。结果:在相对分子质量56kDa处出现HPV16L1的特异性条带;电镜下可见病毒样颗粒在昆虫细胞的核内形成;优化型HPV16L1基因的表达水平显著高于野生型。High Five细胞表达的最佳条件为MOI=10,表达时相72h,其L1蛋白表达量至少比Sf9细胞高3倍。结论:密码子优化技术确实能够促进HPV16L1蛋白的高效表达,而High Five细胞表现出的显著优势尤其值得关注。 Objective: To enhance the expression level of human papillomavirus (HPV) 16 L1 through Baculovirus Expression System, in order to lay a foundation of development of prophylactic HPV vaccines. Methods :The codon usage of wild type HPV16L1 gene was optimized according to the codon bias of insect cells. In order to infect both Si9 and High Five insect cells, the recombinant baculovirus was obtained using Baeulovirus Expression System. The expressed product was identified by Western blot;The virus -like particles (VLPs) of HPV16 was confirmed by electron microscopy ;And ELISA was used to evaluate the effect of the optimized gene as well as to determine the optimal expression condition. Results: The expressed protein, with a relative molecular mass of 56kDa, showed specific reaction with HPV16L1 antiserum; The intranuclear VLPs of HPV16L1 were observed by electron microscopy; The result of ELISA indicated that the expression level of optimized HPV16L1 gene was significantly higher than the wild type; And the optimal expression condition for High Five cells was determined as MOI 10 and expression phase 72 hours, in which the L1 protein was expressed at least 3 times higher than that in sf9 cells. Conclusion: Codon optimization could indeed enhance the expression level of HPV16L1 gene in insect cells. The significant advantage of High Five cells was worth attention.
出处 《中国生物工程杂志》 CAS CSCD 北大核心 2009年第7期27-32,共6页 China Biotechnology
关键词 HPV16L1 密码子优化 重组杆状病毒 SF9细胞 HIGH Five细胞 HPV16L1 Codon optimization Recombinant baculovirus Sf9 cells High Five cells
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参考文献12

  • 1Munoz N,Bosch F X,De Sanjose S,et al.Epidemiologic classification of human papillomavirus types associated with cervical cancer.N Engl J Med,2003,348(6):518-527.
  • 2Zhou J,Sun X Y,Stenzel D J,et al.Expression of vaccinia recombinant HPV16 L1 and L2 ORF proteins in epithelial cells is sufficient for assembly of HPV virion-like particles.Virology,1991,185(1):251-257.
  • 3Widdce L E,Kahn J A.Using the new HPV vaccines in clinical practice.Cleve Clin J Med,2006,3(10):929-935.
  • 4Steinbrook R.The potential of human papillomavirus vaccines.New Eng J Med,2006,354:1109-1111.
  • 5Franco E L,Harper D M.Vaccination against human papillomavirus infection:a new paradigrn in cervical cancer control.Vaccine,2005,23(17-18):2388-2394.
  • 6王淼,宋国兴.人乳头瘤病毒的病毒样颗粒的生产方法:中国,02149970.5.2004-05-26.
  • 7Baud D,Benyacoub J,Revaz V,et al.Immunogenieity asainst human papillomavirus type 16 virus-like particles is strongly enhanced by the PhoPc phenotype in Salmonella enterica serovar Typhimurium.Infect Immun,2004,72(2):750-756.
  • 8杨筱凤,陈宏伟,郑瑾,司履生,董小平,王一理.人乳头瘤病毒16L1-减毒志贺氏杆菌为载体疫苗的构建及免疫效应初步鉴定[J].病毒学报,2005,21(3):198-203. 被引量:5
  • 9闫爱丽,郑瑾,来保长,耿宜萍,张润歧,王一理.人乳头瘤病毒18型L_1基因果蝇表达系统的构建和鉴定[J].陕西医学杂志,2007,36(8):943-945. 被引量:3
  • 10Shpaer E G.Constraints on cedon context in Escherichia coli genes.Their possible role in modulating the efficiency of translation.J Mol Biol,1986,188(4):555-564.

二级参考文献6

  • 1JinZHENG JunMA Xiao-FengYANG Hong-WeiCHENG Lu-ShengSIt Yi-LiWANG.Highly Efficient and Economical Baculovirus Expression System for Preparing Human Papillomavirus Type16 Virus-like Particle[J].Acta Biochimica et Biophysica Sinica,2004,36(8):548-552. 被引量:7
  • 2Angelichio PL,Beck JA,Johansen H,et al.Comparison of Several Promoters and Polyadenylation Signals for Use in Heterologous Gene Expression in Culyured Drosophila Cells.Nucleic Acids Res,1991,19:5037.
  • 3BunchT A,Grinblat Y,Goldstein LS.Characterization and Use of the Meallothionein Promoter in Cultured Drosophila melanogaster cells.Nucleic Acids,1988,16:1043,
  • 4Lilie H,Schwarz E,Rudolph R.Advances in refolding of proteins produced in E.coli.Cur Opin Biot,1998,9:442.
  • 5Gribskov M,Burgess RR.Overexpression and purification of the sigma subunit of E.coil RNA polymerase.Gene,1983,26:109.
  • 6Chen Y,Ghim SJ,Jenson AB,et al.Mutant canine oral papillomavirus L1 capsid proteins which form virus-like particles but lack native conformational epitopes.J Gen Virol,1998,79(Pt9):2137.

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