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作 者:苏胖胖 孟令文[1] 李江艳[1] 陶志勇[1] 陈勇[1] 乔继琛 武肖肖 金赟[1] 王好鹏[1] 方强[1] 王雪梅[1] 夏惠[1]
机构地区:[1]蚌埠医学院病原生物学教研室、安徽省感染与免疫重点实验室,蚌埠233030
出 处:《中国血吸虫病防治杂志》2016年第1期34-38,共5页Chinese Journal of Schistosomiasis Control
基 金:蚌埠医学院研究生科研创新计划资助项目(Byycx1402);安徽省教育厅自然科学研究重点项目(KJ2012-A-200);安徽省大学生创新训练计划项目(AH201410367046,AH201410367041);国家级大学生创新训练计划项目(201410367046,201410367041)
摘 要:目的克隆恶性疟原虫配子体期特异性基因(Plasmodium falciparum gametocyte development 1 gene,Pfgdv1),体外表达和鉴定重组Pfgdv1蛋白。方法通过PCR法从恶性疟原虫感染病人血液DNA样本中扩增Pfgdv1基因,插入到原核表达载体p ET28a(+),构建p ET28a-Pfgdv1重组表达质粒,转化至大肠埃希菌(E.coli)BL21(DE3+),通过异丙基-β-D-硫代吡喃半乳糖苷诱导表达重组蛋白,经Ni+-亲和层析柱纯化重组蛋白,纯化产物经十二烷基磺酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和Western blotting鉴定。结果 PCR扩增的Pfgdv1基因长度约为1.65 kb,重组p ET28a-Pfgdv1质粒构建成功,插入方向正确无框移,转化至E.coli BL21(DE3+)所表达的重组蛋白分子量约为67 k Da,且能被抗His标签单克隆抗体识别。结论成功克隆了Pfgdv1基因,表达并纯化了重组Pfgdv1蛋白,为进一步研究恶性疟原虫配子体期传播阻断疫苗奠定了基础。Objective To clone a gametocyte specific protein Pfgdvl of Plasmodium falciparum, express and identify recombinant Pfgdvl protein in vitro. Methods PCR was performed to amplify Pfgdvl from P. falciparum DNA which was got from the patient who was infected with P. falciparum, and the PCR product was inserted into pET28a (+) vector, pET28a-Pfgdvl recombinant plasmid was constructed and transformed into E. coli host BL21 (DE3+). IPTG was used to induce the recombi- nant Pfgdvl protein fused with His tag, and the protein was purified by His-NTA affinity chromatography. The recombinant pro- tein was identified by SDS-PAGE and Western blotting. Results The PCR product of Pfgdvl gene was about 1.65 kb, meeting the expectation of predicted fragment size. The recombinant protein was about 67 kDa, which could be recognized by His-Tag monoclonal antibody. Conclusion The Pfgdvl gene of P. falciparum is successfully cloned, and the recombinant Pfgdvl protein is expressed, thereby providing an opportunity for further study on transmission blocking vaccine.
关 键 词:恶性疟原虫 Pfgdv1 配子体 传播阻断疫苗 原核表达
分 类 号:R382.31[医药卫生—医学寄生虫学]
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