流感病毒多表位基因盒的设计与预测
Design and prediction of multi-epitope gene of influenza A virus
作者:邵京京;丰锋;张强;李虹;李明远;王保宁;李婉宜;
Author:
收稿日期: 年卷(期)页码:2012,27(05):-486-489
期刊名称:华西药学杂志
Journal Name:WEST CHINA JOURNAL OF PHARMACEUTICAL SCIENCES
关键字:流感病毒;抗原表位;生物信息学分析;多表位基因盒
Key words:
基金项目:国家自然科学基金(批准号:30973235);;
四川省科技支撑项目(批准号:2010SZ0110)
中文摘要
目的预测流感病毒抗原表位并设计合成多表位基因盒。方法收集不同类型流感病毒基因序列,联合运用Syf-peithi、ProPred、Multipred2、Bcepred、Clastal X1.83、SWISS-MODEL等多种生物信息学软件进行分析,预测流感病毒Matrix1(M1)、Matrix2(M2)、Nucleoprotein(NP)和HA蛋白上的抗原表位,设计并合成流感病毒多表位基因盒。结果在不同亚型流感病毒的HA蛋白抗原上成功筛选出2个B细胞表位,在M1、M2及NP蛋白上分别筛选出3个T细胞表位,以一定的间隔序列串联各表位,设计并合成流感多表位基因盒。预测结果显示该多表位基因盒具有良好的同源性及抗原性。结论成功设计出包含T细胞表位及B细胞表位的流感病毒多表位基因盒Eg,为流感多表位基因疫苗的研发奠定了基础。
参考文献
[1]Zhong W,Chem JB.Genome-wide characterization of a viral cy-totoxic T lymphocyte epitope repertoire[J].J Biol Chem,2003,278:45135-45144.
[2]Crowe SR,Miller SC,Brown DM,et al.Uneven distribution ofMHC classII epitopes within the in uenza virus[J].Vaccine,2006,24:457-467.
[3]Li H,Ding J,Chen YH.Recombinant protein comprising multi-neutralizing epitopes induced high titer of antibodies against influ-enza A virus[J].Immunobiology,2003,207:305-313.
[4]Lu Y,Ding J,Liu W,et al.A candidate vaccine against influenzavirus intensively improved the immunogenicity of a neutralizingepitope[J].Int Arch Allergy Immunol,2002,127:245-250.
[5]Deliyannis G,Jackson DC,Ede NJ,et al.Induction of long-termmemory CD8(+)T cells for recall of viral clearing responses a-gainst influenza virus[J].J Virol,2002,76:4212-4221.
[6]Lawrence CW,Ream RM,Braciale TJ.Frequency,specificity,andsites of expansion of CD8+T cells during primary pulmonary in-fluenza virus infection[J].J Immunol,2005,174:5332-5440.
[7]Berkhoff EGM,Geelhoed-Mieras MM,Fouchier RAM,et al.Assessment of the extent of variation in influenza A virus cytotoxicT-lymphocyte epitopes by using virus-specific CD8+T-cellclones[J].J Gen Virol,2007,88:530-535.
[8]Kreijtz JHCM,Bodewes R,Brand JMA,et al.Infection of micewith a human influenza A/H3N2 virus induces protective immu-nity against lethal infection with influenza A/H5N1 virus[J].Vaccine,2009,27:4983-4989.
[9]Khan N,Hislop A,Gudgeon N,et al.Herpesvirus-specific CD8T cell immunity in old age:Cytomegalovirus impairs the responseto a coresident EBV infection[J].J Immunol,2004,173(12):7481-7489.
[10]Toebes M,Coccoris M,Bins A,et al.Design and use of condi-tional MHC class I ligands[J].Nat Med,2006,12:246-251.
[11]Zhong W,Reche PA,Lai CC,et al.Genome-wide characteriza-tion of a viral cytotoxic T lymphocyte epitope repertoire[J].J BiolChem,2003,278:45135-45144.
[12]Cheuk E,Chamberlain JW.Strong memory CD8+T cell respon-ses against immunodominant and three new subdominant HLA-B27-restricted influenza A CTL epitopes following secondary in-fection of HLA-B27 transgenic mice[J].Cell Immunol,2005,234:110-123.
[13]Zou P,Liu W,Wu F,et al.Fine-epitope mapping of an antibodythat binds the ectodomain of influenza matrix protein 2[J].FEMS Immunol Med Microbiol,2008,53:79-84.
[14]Tourdot S,Herath S,Gould KG.Characterization of a new H-2D(k)-restricted epitope prominent in primary influenza A virusinfection[J].J Gen Virol,2001,82:1749-1755.
[15]Rammensee H,Bachmann J,Emmerich NP,et al.Database forsearching and T-cell epitope prediction immunoinformatics[J].Methods in Mole Biology,2007,409:75-93.
[16]张有峰,王红宁,黄勇,等.多表位疫苗的构建策略及其在动物疫苗中的应用[J].中国农业科技导报,2008,10(2):29-33.
【关闭】