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利用串联亲和纯化技术分离大肠杆菌GroEL蛋白复合物
引用本文:魏波,廖翔,周围,王羽,李玉霞,高原,岳俊杰,梁龙,呼和巴特尔.利用串联亲和纯化技术分离大肠杆菌GroEL蛋白复合物[J].微生物学通报,2011,38(12):1848-1854.
作者姓名:魏波  廖翔  周围  王羽  李玉霞  高原  岳俊杰  梁龙  呼和巴特尔
作者单位:1. 内蒙古农业大学兽医学院 内蒙古呼和浩特010018;军事医学科学院生物工程研究所 北京 100071
2. 军事医学科学院生物工程研究所 北京 100071
3. 内蒙古农业大学兽医学院 内蒙古呼和浩特010018
基金项目:国家自然科学基金项目(No. 30970122)
摘    要:肠出血性大肠杆菌O157∶H7是一种重要的致病菌,加深其致病机理的基础研究将为相关疫苗研究及疾病控制等提供新的思路和依据.串联亲和纯化(TAP)技术是最近发展的分离纯化天然状态蛋白质复合物进而研究蛋白质相互作用的新方法.用我们自己构建的原核表达串联亲和标签载体,在大肠杆菌O157∶H7中表达了标签融合蛋白GroEL-TAP,建立了非变性条件下制备蛋白复合物的方法,并且对串联亲和纯化过程中的相关实验条件进行了探索和优化,最终得到了高纯度的GroEL-TAP与天然GroEL形成的嵌合型多聚体复合物.这表明我们建立的串联亲和纯化技术能高度特异地纯化靶蛋白参与形成的复合物,为后续寻找O157∶H7中毒力蛋白参与形成的复合物奠定了实验基础.

关 键 词:肠出血性大肠杆菌O157∶H7  串联亲和纯化(TAP)  分子伴侣GroEL

Application of tandem affinity purification technique for separation of GroEL complexes in Escherichia coli
WEI Bo,LIAO Xiang,ZHOU Wei,WANG Yu,LI Yu-Xi,GAO Yuan,YUE Jun-Jie,LIANG Long and HUHE Bateer.Application of tandem affinity purification technique for separation of GroEL complexes in Escherichia coli[J].Microbiology,2011,38(12):1848-1854.
Authors:WEI Bo  LIAO Xiang  ZHOU Wei  WANG Yu  LI Yu-Xi  GAO Yuan  YUE Jun-Jie  LIANG Long and HUHE Bateer
Institution:1. College of Veterinary Medicine, Inner Mongolia agricultural University, Hohhot, Inner Mongolia 010018, China; 2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;1. College of Veterinary Medicine, Inner Mongolia agricultural University, Hohhot, Inner Mongolia 010018, China; 2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;2. Institute of Biotechnology, Academy of Military Medical Sciences, Beijing 100071, China;1. College of Veterinary Medicine, Inner Mongolia agricultural University, Hohhot, Inner Mongolia 010018, China
Abstract:Enterohemorrhagic Escherichia coli O157:H7 is a kind of important pathogenic bacterium, and deeper studies of molecular pathogenesis will contribute better to related vaccine research and disease control. Tandem affinity purification (TAP) technique is a kind of new method which was recently developed and used to separate and purify native protein complexes and so on to study interactions between proteins. In this study, a prokaryotic TAP expression vector constructed by our laboratory was successfully used to express fusion protein GroEL-TAP in Enterohemorrhagic Escherichia coli O157:H7. An efficient method for preparation of native protein complexes was developed and all experimental parameters of tandem affinity purification were optimized. The highly pure protein complexes com-posed of both tagged GroEL-TAP and natural GroEL were obtained with our expression and purification system. These results showed that our TAP system worked well to specifically purify protein complex participated with target protein in Enterohemorrhagic Escherichia coli O157:H7. This study provided satisfactory experimental base for follow-on works on identifying virulence protein participated com-plexes.
Keywords:Enterohemorrhagic Escherichia coli O157:H7  Tandem affinity purification (TAP)  Chaperonin GroEL
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