GST/AEP融合蛋白原核表达载体的构建、表达及鉴定  被引量:1

Construction and expression of prokaryotic expression vector of GST/AEP fusion protein and identification

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作  者:高碧峰[1] 王宗仁[1] 张德安[1] 

机构地区:[1]第四军医大学西京医院中医科,陕西西安710032

出  处:《现代生物医学进展》2006年第8期1-3,共3页Progress in Modern Biomedicine

基  金:国家自然科学基金资助项目(30671764)

摘  要:目的:为进一步研究抗癫痫肽(Anti-epilepsy peptide,AEP)的抗痫机制及筛选其相关作用蛋白,进行GST/AEP融合蛋白原核表达载体的构建及融合蛋白的表达。方法:通过PCR基因扩增对AEP基因进行扩增,并将其克隆于谷胱甘肽-S-转移酶(GST)融合蛋白表达质粒pGEX-4T-1中,经酶切、序列鉴定分析后,用该重组质粒转化大肠杆菌Bl21(DE3),经IPTG诱导获得表达,并采用Western Blot进行检测。结果:成功构建了AEP原核表达载体,并在大肠杆菌Bl21中获得表达。结论:成功构建了GST/AEP原核表达载体,并表达了GST/AEP融合蛋白。Objective: To express fusion protein of GST and Anti- epilepsy peptide (AEP) in E. coli. Methods: The core fragment of AEP was cloned into pGEX- 4T- 1 cotaining glutathione s - transterase(GST) fusion protein gene. Following the restriction enzyme digestion analysis and sequencing, pGEX- 4T- 1/AEP was transformed into E. coli BI21 (DE3). GST/AEP fusion protein was expressed under IFTG induction and the AEP protein was identified by the Western - blot. Results: The restriction endonuclease digestion analysis of recombinant plasmid demonstrated that the AEP gene had been exactly inserted in pGEX - 4T- 1, SDS - PAGE analysis showed that the relative molecular mass of the fusion protein was about 34KD. The GST/AEP fusion protein was expressed in E.coli B121(DE3)and identified by the Western- blot. Conclusion: pGEX- 4T- 1/AEP vector was successfully constructed, and the GST/AEP fusion protein in E. coli BI21 (DE3)was expressed.

关 键 词:抗癫痫肽 GST-融合蛋白 原核表达 基因扩增 

分 类 号:R742.1[医药卫生—神经病学与精神病学]

 

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