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作 者:王海[1] 胡少敏[1] 黄艳[1] 吕刚[1] 吴忠道[1] 余新炳[1]
机构地区:[1]中山大学基础医学院寄生虫学教研室,广州510089
出 处:《中国人兽共患病杂志》2005年第8期656-659,共4页Chinese Journal of Zoonoses
基 金:国家自然科学基金(30271165);教育部博士点基金(20020558059);广东省自然科学基金(031727)。
摘 要:目的构建日本血吸虫的翻译控制肿瘤蛋白(SjTCTP)基因的杆状病毒重组供体质粒pFASTA-TCTP,用该重组转移质粒转化含有杆状病毒表达载体以构建BacmidGFP-TCTP,感染昆虫细胞进行表达。方法将已克隆的SjTCTP基因与线性化的pFASTA进行连接为pFASTA-TCTP,使pFASTA-TCTP与DH10BAC感受菌进行转座重组,利用抗性及蓝白斑筛选重组BacmidGFP-TCTP克隆,提取BacmidGFP-TCTP转染昆虫细胞Sf9获得有感染力的病毒,利用病毒感染Sf9细胞进行蛋白表达,通过荧光镜观察、RT-PCR、SDS-PAGE和Western-Blotting检测表达情况。结果获得了重组SjTCTP的杆状病毒,细胞能表达出与SjTCTP单抗结合的、分子量为23kDa左右的融合有组氨酸标签的目的蛋白。结论SjTCTP能在昆虫细胞中获得良好表达,为其的分子生物学活性研究奠定了基础。To construct the Baculovirus expression vector for translationaUy controlled tumor protein (TCTP) gene of Schistosoma japonicum and to express in insect sf9 cell line, the TCTP eDNA was cloned into plasmid pFASTA, and therecombinant plasmid was transformed to competent cells DH10Bat. A transformant containing the target gene was obtained and named as BacmidGFPSjTCTP. After transfecting this transformant into Sf9 cells, its expression in Sf9 cells was detected by fluorescent microscopic examination, RT-PCR, SDS-PAGE and Western blotting. The experimental results showed that the recombinant buculovirns was obtained and the transformant BacmidGFP-SjTCTP was expressed in insect Sf9 cells. This recombinant transformant can be used as the protein accessed high biological characteristics for the functional study on TCTP of S. japonicum.
关 键 词:日本血吸虫 SjTCTP 杆状病毒表达载体 SF9细胞
分 类 号:R383.2[医药卫生—医学寄生虫学]
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