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恶性疟原虫FCC1/HN株P190抗原保守区基因的克隆及其在大肠杆菌中的表达
引用本文:杨树桐,潘卫庆.恶性疟原虫FCC1/HN株P190抗原保守区基因的克隆及其在大肠杆菌中的表达[J].高技术通讯,1994,4(3):32-35.
作者姓名:杨树桐  潘卫庆
作者单位:上海第二军医大学医学生物技术和分于遗传研究所
基金项目:联合国开发计划署,世界银行,世界卫生组织
摘    要:P190是恶性疟原虫裂殖子表面抗原,是很有希望的疟疾疫苗候选抗原。采用PCR方法克隆了我国海南省FCC1/HN株P190抗原基因的3个保守区片段,连接到pUC18载体上进行DNA序列测定,然后分别与表达载体pGEX-2T连接,经双酶切鉴定后转化感受态JM109大肠杆菌进行高效融合表达。

关 键 词:恶性疟原虫  P190抗原  基因表达

Cloning and Expression of Three Conserved Regions on P190Antigen of Plasmodium Falciparum in E. Coli
Yang Shutong, Pan Weiqing, Deng Hailin, Lu Deru.Cloning and Expression of Three Conserved Regions on P190Antigen of Plasmodium Falciparum in E. Coli[J].High Technology Letters,1994,4(3):32-35.
Authors:Yang Shutong  Pan Weiqing  Deng Hailin  Lu Deru
Affiliation:(received Nov. 3,1993 )Yang Shutong, Pan Weiqing, Deng Hailin, Lu Deru(Institute of Medical Biotechnology and Molecular Genetics,Shanghai,2004 33 )
Abstract:90-kilodalton glycoprotein (P190) of Plasmodium falciparum, precursor of the major surface proteinof merozoites, is considered a promising candidate for blood stage malaria vaccine. We designed six primersaccording to the sequence of MAD20 strain. Three DNA fragments, named as P190 CR2-2, P190 CR3,P190 CR4, respectively, which encoded amino acid residues of conserved region , and on theP190 Antigen, were amplified by polymerase chain reaction from genomic DNA in FCC1/HN strain ofplasmodium falciparum isolated from Hainan Province, China. The amplified fragments were subclonedinto pUC18 vector and sequenced. Those three sequenced fragments inserted into pGEX-2T plasmid . E.colt JM109 (DE3 ) were transformed with the recombinant plasmids. The results show that the threefragments were expressed at high level as C-terminal fusions with glutathione S-trabsferase.
Keywords:: Plasmodium falciparum  Merozoite surface antigen 1  Malaria vaccine
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