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作 者:潘朋歌 李克生[2] 杜惠芬[2] 曾潮宁 PAN Peng-ge;LI Ke-sheng;DU Hui-fen(Fertility Maintenance Key Laboratory of Ministry of Education,Ningxia Medical University/Key Laboratory of Reproduction and Genetics in Ningxia Hui Autonomous Region,Yinchuan,Ningxia 750004;Medical Biotechnology Research Center,Gansu Academy of Medical Sciences,Lanzhou,Gansu 730050)
机构地区:[1]宁夏医科大学生育力保持教育部重点实验室/宁夏回族自治区生殖与遗传重点实验室,宁夏银川750004 [2]甘肃省医学科学研究院医学生物技术研究中心,甘肃兰州730050 [3]兰州雅华生物技术有限公司,甘肃兰州730050
出 处:《安徽农业科学》2018年第30期99-101,共3页Journal of Anhui Agricultural Sciences
摘 要:[目的]原核表达并纯化柯萨奇病毒A组16型(CVA16) VP1蛋白。[方法]根据Gen Bank CVA16 VP1基因序列,合成VP1全基因,连接到载体p ET30a,构建原核表达质粒p ET30a-CVA16-VP1。将测序正确的重组质粒转化至大肠杆菌BL21(DE3),IPTG诱导蛋白表达,Ni-NTA亲和层析纯化,SDS-PAGE和Western Blot鉴定重组蛋白。[结果]成功构建重组质粒p ET30a-CVA16-VP1,表达蛋白经SDS-PAGE显示分子量约为38.7 k Da,目的蛋白以包涵体形式存在,蛋白经复性、纯化,纯度达90%以上;经Western Blot检测,证实表达的蛋白为VP1蛋白。[结论]成功获得了高纯度的VP1蛋白,为此抗原用于临床诊断打下了基础。[Objective]To express and purify the VP1 protein of coxsackie virus group A 16 strain (CVA16) in E.coli. [Method]The CVA16 VP1 gene was manually synthesized according to the GenBank VP1 sequence,and then cloned into pET30a to construct the expressional plasmid pET30a- CVA16-VP1. The plasmid pET30a- CVA16-VP1 confirmed through sequencing was transformed into E.coli BL21 (DE3) for inducing VP1 expression by IPTG and purification by Ni-NTA affinity chromatography.The purified protein was identified by SDS-PAGE and Western Blot.[Result]The recombinant plasmid pET30a- CVA16-VP1 was obtained.The relative molecular mass of the protein was 38.7 kDa by SDS-PAGE analysis.The target protein existed as inclusion bodies.The purity of the purified protein was above 90%.Western Blot proved that the expressed product is VP1 protein.[Conclusion]The recombinant CVA16 VP1 protein was successfully expressed in E.coli, which laid a solid foundation for the clinical diagnosis of MTB infection.
关 键 词:柯萨奇病毒A组16型(CVA16) VP1蛋白 原核表达 纯化
分 类 号:R373.23[医药卫生—病原生物学]
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