CAJ | 학술논문

克隆、表达和鉴定猪流感病毒H1N1 HA,NA基因序列,为制备抗体和基因工程疫苗打下基础.在成功克隆猪流感病毒H1N1全长HA、NA基因并测序的基础上,将部分基因序列克隆到表达载体pET32a(+)上,全基因序列克隆到表达载体pGEX4T-1上,构建了重组表达质粒pET32a(+)/HA(截短),pET32a(+)/NA(截短),pGEX4T-1/NA,转化大肠杆菌BL2.1/Rosetta,IPTG诱导表达,利用Ni~(2+)亲和层析柱和GSTrap 4B亲和层析柱对重组蛋白进行纯化.并用Western Blotting和ELISA方法检测其抗原性.结果显示,重组蛋白在大肠杆菌中可以高效表达,SDS-PAGE显示其相对分子质量与预计大小一致.ELISA和Western blotting试验证实,重组蛋白具有良好的抗原性.本研究成功克隆和表达了猪流感病毒H1N1 HA、NA基因序列,为猪流感病毒H1N1诊断试剂和疫苗的开发等进一步的研究奠定了基础.
극륭、표체화감정저류감병독H1N1 HA,NA기인서렬,위제비항체화기인공정역묘타하기출.재성공극륭저류감병독H1N1전장HA、NA기인병측서적기출상,장부분기인서렬극륭도표체재체pET32a(+)상,전기인서렬극륭도표체재체pGEX4T-1상,구건료중조표체질립pET32a(+)/HA(절단),pET32a(+)/NA(절단),pGEX4T-1/NA,전화대장간균BL2.1/Rosetta,IPTG유도표체,이용Ni~(2+)친화층석주화GSTrap 4B친화층석주대중조단백진행순화.병용Western Blotting화ELISA방법검측기항원성.결과현시,중조단백재대장간균중가이고효표체,SDS-PAGE현시기상대분자질량여예계대소일치.ELISA화Western blotting시험증실,중조단백구유량호적항원성.본연구성공극륭화표체료저류감병독H1N1 HA、NA기인서렬,위저류감병독H1N1진단시제화역묘적개발등진일보적연구전정료기출.
It was to clone,express and characterize the HA and NA Protein of Swine influenza virus H1N1.On the basis of successful cloning the full length HA and NA gene,part of the gene into pET32a(+)were ligated,and full of the gene into pGEX4T-1.An expression vector pET32a(+)/HA(cut),pET32a(+)/NA(cut),pGEX4T-1/NA were constructed and expressed in E.coli BL21/rosetta induced by IPTG.Recombinant protein was purified through affinity chromatography column.Western Blotting and ELISA were used to determine the antigenic of the recombinant protein.Results showed that the recombinant capsid gene can be over expressed in Ecoli.SDS-PAGE showed that the gene could express product as same as expected.ELlSA and Western blotting showed that the recombinant protein performed satisfactory antigenic.Therefore,the HA and NA protein of swine influenza virus H1N1 has been successful cloned and expressed,which could be useful for developing diagnose reagents or vaccine of H1N1.