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作 者:黄朋[1] 赵帅杰[1] 陆慧君[1] 尹继刚[1] 姜宁[1] 陈启军[1] HUANG Peng ZHAO Shuaijie LU Huijun YIN Jigang JIANG Ning CHEN Qijun(Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun 130062, China)
机构地区:[1]吉林大学人兽共患病研究所,人兽共患病研究教育部重点实验室,长春130062
出 处:《吉林农业大学学报》2017年第1期100-105,共6页Journal of Jilin Agricultural University
基 金:国家自然科学基金项目(81130033)
摘 要:为研究肝素结合蛋白质PF3D7_1104400的功能以及其作为疟疾疫苗候选抗原的可行性,通过PCR方法扩增目的基因,并将其与p ET-28a和p GEX-4T-1表达载体连接构建重组表达质粒。将构建成功的重组表达质粒转化入大肠杆菌BL21-Condon Plus(DE3)-RIPL中诱导表达,利用亲和层析的方法纯化His-tag和GSTtag重组蛋白质。用His-tag重组蛋白质免疫家兔制备多克隆抗体,以该抗体为一抗,利用Western blot检测该抗体的特异性以及PF3D7_1104400蛋白质在虫体内是否表达。结果表明:成功构建重组表达质粒PF3D7_1104400-p ET和PF3D7_1104400-p GEX,诱导表达并纯化出特异性好、纯度高的重组蛋白。制备的多克隆抗体能够特异性识别虫体天然蛋白,PF3D7_1104400蛋白质在恶性疟原虫体内全长表达。To research the biological function of heparin binding protein PF3D7_1104400 and its feasibility as candidate vaccine antigen,target gene was amplified by PCR whose products were connected with p ET-28 a and p GEX-4T-1 for constructing recombinant expression plasmids. Transformed into BL21-Condon Plus( DE3)-RIPL,recombinant plasmids were induced and expressed and recombinant proteins were purified by the method of affinity chromatography. Polyclonal antibody was prepared by rabbits immuned with His-tagged recombinant proteins. The specificity of antibody and expression of PF3D7_1104400 were detected by Western blot in which polyclonal antibody was used as primary antibody. The results showed that recombinant plasmids,PF3D7_1104400-p ET and PF3D7_1104400-p GEX,were constructed successfully and specific recombinant proteins were expressed and purified. According to the results of Western blot,natural protein of PF3D7_1104400 could be recognized specifically by prepared antibody and was expressed in Plasmodium falciparum in the form of total length,which will lay foundation for further research of PF3D7_1104400.
关 键 词:恶性疟原虫 肝素 原核表达 多克隆抗体 疫苗候选抗原
分 类 号:S855.99[农业科学—临床兽医学]
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