摘要
目的:构建重组人白细胞介素7(rhIL-7)的原核表达载体,在大肠杆菌中表达并鉴定。方法:以RT-PCR方法扩增编码IL-7的cDNA片段,插入至pET-3d载体中,构建rhIL-7的原核表达载体,阳性克隆经测序鉴定,转化至大肠杆菌BL21(DE3),优化rhIL-7表达条件,利用免疫印迹鉴定重组蛋白。结果:重组载体经DNA测序显示包含正确的rhIL-7编码序列,重组载体转入大肠杆菌后,经IPTG诱导后外源蛋白表达,相对分子质量为17 400,与IL-7理论分子质量一致;免疫印迹显示,外源蛋白可以被人IL-7特异性抗体识别,表明在原核表达的外源蛋白是rhIL-7。rhIL-7主要表达于包涵体中,包涵体表达优化条件为:温度为37℃、IPTG浓度为0.4 mmol/L、诱导时间为4h。结论:成功的构建了rhIL-7的原核表达载体。
Aim：To construct a prokaryotic expression vector for human interleukin7（IL-7）,identify its expression product and optimize its expression condition. Methods： The cDNA fragment encoding human IL-7 was amplified by RT-PCR from the total RNA of human PBMC,and then the IL-7 gene was cloned into pET-3d plasmid to construct a prokaryotic expression vector.The positive clone was analyzed by DNA sequencing.The recombinant protein was expressed in Escherichia coli（E.coli） BL21（DE3） strain and identified with Western blotting.Results： The prokaryotic expression vector forIL-7 was constructed and confirmed by sequencing.The expression vector was transformed into E.coli and was expressed in after induction with IPTG.The relative molecular weight of the protein was 17 400,which is consistent with theoretical value.Western blotting showed that the recombinant protein was mainly presented in inclusion bodies.The optimized expression condition was 4 h induction at 37 ℃ with 0.4 mmol/L IPTG.Conclusion：The prokaryotic expression vector for human IL-7 has been constructed successfully and the expression condition has been optimized,which has paved the way for further study on human IL-7.
出处
《暨南大学学报（自然科学与医学版）》
CAS
CSCD
北大核心
2010年第4期331-335,共5页
Journal of Jinan University(Natural Science & Medicine Edition)
基金
国家自然科学基金项目(30572199
30371651)
