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作 者:王萍[1,2] 李明[1,2] 谢毅 殷明[1,2] 李英杰
机构地区:[1]中国人民解放军第一军医大学热带病研究室 [2]上海复旦大学遗传所国家重点实验室基因合成室
出 处:《寄生虫与医学昆虫学报》1999年第1期12-17,共6页Acta Parasitologica et Medica Entomologica Sinica
基 金:上海市青年科技启明星计划资助
摘 要:本文根据抗原分子特性,用限制性内切酶HpaⅠ和EcoRⅠ及三对XhoⅠ-EcoRⅠ接头,对β-半乳糖苷酶融合蛋白表达载体pWR450进行了改建,截去其β-半乳糖苷酶C端约300个氨基酸的编码序列,构建了一组含β-半乳糖苷酶N端146个氨基酸编码序列的pWX146融合蛋白表达载体,以pWX146-Ⅰ作为载体。We have constructed a pWX146 family based on pWR450,a β galactosidase fusion protein expression vector.The pWX146 family is consisted of pWX146,pWX146 1 and pWX146 2.Each of them includes a lac promoter of E.coli,a truncated sequence encoding 146 amino acids at the N terminus of β galactosidase and a different poly linker sequence.A 306bp gene fragment,encoding repetitive region of histidine rich protein Ⅱ(HRP Ⅱ) of Plasmodium,falcipatum was cloned into pWX146 1 and efficiently expressed fusion protein after induction with IPTG in E.coli.The truncation of the sequence encoding β galactosidase minimized influence on the stucture and expression of the expected target peptides,therefore the pWX146 family may also be useful for epitope analysis using sequential deletion strategy.
分 类 号:R382.31[医药卫生—医学寄生虫学] Q78[医药卫生—基础医学]
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