Li Jin, Cui Yong, Yin Kun, Liu Gong-zhen, Xiao Ting, Xu Chao, Wei Qing-kuan, Huang Bing-cheng, Sun Hui
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2016 Jun;34(3):198-202.
To prokaryotically express three gene fragments of micronemal protein 16 (TgMIC16) of Toxoplasma gondii, and analyze the immunoreactivity of the three recombinant protein products.
Primers were designed for three fragments of TgMIC16 gene which encode proteins within the functional domain. Reverse-transcription PCR was used to generate cDNA from RNA, and the three fragments were amplified on the cDNA by PCR using the designed primers. The PCR products were double-digested, inserted into the pET-32a(+) plasmid, and transformed into Escherichia coli TOP10 cells. Plasmids extracted from positive clones were confirmed by BamHⅠ/HindⅢ double digestion and sequencing, and further transformed into E. coli Rosetta cells. Protein expression was induced by IPTG, and confirmed by SDS-PAGE. The expressed recombinant proteins were purified with Ni-NTA affinity chromatography and their immunoreactivity analyzed with Western blotting.
The amplified three fragments were 1 806, 1 290 and 855 bp in size. Double digestion and sequencing results confirmed the successful construction of the three recombinant plasmids. SDS-PAGE analysis showed successful expression of the three recombinant proteins (M(r) 88 000, 68 000 and 52 000, respectively), in the form of inclusion bodies. Western blotting showed that the three purified recombinant proteins reacted with His monoclonal antibody and rabbit anti-T. gondii antibody.
The three fragments within the functional domain of TgMIC16 are successfully expressed in prokaryotic expression system and show immunoreactivity.
原核表达刚地弓形虫微小膜蛋白16(TgMIC16)的3个基因片段,并分析这3种重组蛋白产物的免疫反应性。
针对TgMIC16基因编码功能域内蛋白质的3个片段设计引物。采用逆转录PCR从RNA生成cDNA,使用设计的引物在cDNA上扩增这3个片段。对PCR产物进行双酶切,插入pET-32a(+)质粒,转化至大肠杆菌TOP10细胞。从阳性克隆中提取的质粒经BamHⅠ/HindⅢ双酶切和测序确认,进一步转化至大肠杆菌Rosetta细胞。用异丙基-β-D-硫代半乳糖苷(IPTG)诱导蛋白表达,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)进行确认。用镍-亚氨基二乙酸(Ni-NTA)亲和层析法纯化表达的重组蛋白,并用蛋白质免疫印迹法分析其免疫反应性。
扩增得到的3个片段大小分别为1 806、1 290和855 bp。双酶切和测序结果证实3种重组质粒构建成功。SDS-PAGE分析显示3种重组蛋白均成功表达(相对分子质量分别为88 000、68 000和52 000),以包涵体形式存在。蛋白质免疫印迹法显示,3种纯化的重组蛋白均能与组氨酸(His)单克隆抗体和兔抗刚地弓形虫抗体发生反应。
TgMIC16功能域内的3个片段在原核表达系统中成功表达,并具有免疫反应性。