摘要
本研究将已构建好的、包含口蹄疫病毒P1+2A基因的重组表达质粒pQE-Tri/P1+2A经质脂体2000转染哺乳动物细胞BHK-21,转染后一定时间进行检测。通过SDS-PAGE、Western-blotting、荧光抗体染色、ELISA等检测方法表明,FMDVP1+2A基因片段在BHK-21细胞中成功表达,表达的蛋白能被口蹄疫阳性血清所识别而且具有良好的生物学活性。这一结果的取得,为进一步研制新型口蹄疫基因工疫苗及其配套诊断试剂奠定了基础。
In this study, recombinant expression plasmid pQE-Tri/P1+2A was constructed and then transfected into BHK-21 cell line mediated by liposome 2000. The results of SDS-PAGE, Western-blotting, fluorescence antibody and ELISA showed that FMDV P 1 +2A protein was expressed in BHK-21 cell line successfully and can be recognized by FMD positive serum. The result will lay a foundation for study of FMDV gene engineered vaccines as well as the development of diagnostic reagents.
出处
《中国病毒学》
CSCD
2006年第5期454-457,共4页
Virologica Sinica
基金
国家863高技术研究发展计划(2003AA241110)