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人源抗菌肽LL-37原核表达载体的构建及表达
引用本文:顾银霞,周学章,宋振威,李敏,王玉炯.人源抗菌肽LL-37原核表达载体的构建及表达[J].宁夏大学学报(自然科学版),2008,29(4).
作者姓名:顾银霞  周学章  宋振威  李敏  王玉炯
作者单位:宁夏大学,西部特色生物资源保护与利用教育部重点实验室,宁夏,银川,750021
基金项目:国家重点基础研究发展计划(973计划) 
摘    要:为了使人源抗菌肽LL-37在原核表达载体中获得高效表达,在不改变LL-37氨基酸的基础上,根据大肠杆菌偏爱密码子表,替换LL-37部分密码子,设计一段新的LL-37序列.采用DNA Work设计4条互补引物,利用SOE-PCR技术扩增完整的LL-37目的片段,以pET-PPPI为载体,构建原核表达载体pET-PPPIL,并制备表达菌BL21(DE3)(pET-PPPIL),该菌经诱导高效表达LL-37融合蛋白,为后续纯化LL-37奠定了基础.

关 键 词:聚合酶链式反应  人源抗菌肽LL-37  蛋白表达

Construction of Human Antimicrobial Peptide LL-37 Prokaryotic Expression Vector and Its Expression
Gu Yinxia,Zhou Xuezhang,Song Zhenwei,Li Min,Wang Yujiong.Construction of Human Antimicrobial Peptide LL-37 Prokaryotic Expression Vector and Its Expression[J].Journal of Ningxia University(Natural Science Edition),2008,29(4).
Authors:Gu Yinxia  Zhou Xuezhang  Song Zhenwei  Li Min  Wang Yujiong
Abstract:To make highly expressed human antimicrobial peptide LL-37 in prokaryotic expression system,the part of codon of LL-37 was replaced and a new LL-37 series was designed in this work.Four complementary primers were designed by DNA Work,the integrity of the LL-37 fragment was amplified by SOE-PCR,then expression vector pET-PPPIL was constructed with pET-PPPI as the carrier,and prepared expression strain BL21(DE3)(pET-PPPIL) which is induced expresses LL-37 fusion protein highly,this results lay a foundation for the purifing LL-37.
Keywords:polymerase chain reaction  human antimicrobial peptide LL-37  protein expression
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