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作 者:汤伟松[1] 孟琴[1] 刘亮[1] 李淑珍[1] 唐晓波[1]
机构地区:[1]哈尔滨医科大学药学院生物制药学教研室,150081
出 处:《国际免疫学杂志》2013年第6期480-484,共5页International Journal of Immunology
基 金:哈尔滨市科技创新人才研究专项资金项目(2008RFXXS018)
摘 要:目的重组及表达高免疫原性骨桥蛋白(OPN)的融合蛋白。方法使用Lasergene软件分析OPN基因,选取出免疫原性高的区域作为目的片段。提取总RNA,应用逆转录、PCR等技术扩增OPN基因目的片段,将其分别与带有His标签的pET-32a及GST标签的pGEX-4T-1载体连接。构建表达载体,诱导表达OPN融合蛋白(分别含有His,GST—Tag),并进行SDS—PAGE及Western blotting鉴定。结果扩增后获得一条351bp的DNA片段,经测序鉴定为目的片段序列,并实现了可溶性高表达,经Western blotting鉴定为高免疫原性OPN融合蛋白。结论采用原核表达经纯化后可获得高纯度高免疫原性的OPN融合蛋白,为进一步开发OPN诊断试剂打下基础。Objective To clone and express osteopontin(OPN)fusion proteins with high immunogenic-ity. Methods OPN gene was analyzed using Lasergene software, and a high immunogenic region was selected as target fragment. The fragment of the target gene was cloned by RT-PCR from total RNA, The amplified gene was inserted into vectors pET-32a and pGEX-4T-1. The recombinant plasmids were constructed and expressed proteins (including His-Tag and GST-Tag, respectively) were identified by SDS-PAGE and Western blotting. Results A DNA band about 351 bp was confirmed as target OPN fragment by DNA sequencing. Sohlble ex-pression of high immunogenic OPN fusion proteins was achieved, which was identified by Western blotting. Con-clusion High immunogenic OPN fusion proteins with high purity have been expressed successfully in prokary-otic system. The study lays a foundation for further development of OPN diagnostic reagent.
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