Lu Jia-Xin, Xiang Yang-Fei, Zhang Jia-Xuan, Ju Huai-Qiang, Chen Zhen-Ping, Wang Qiao-Li, Chen Wei, Peng Xin-Lei, Han Bo, Wang Yi-Fei
Biomedicine Research and Development Center, Guangdong Provincial Key Laboratory of Bioengineering Medicine, National Engineering Research Center of Genetic Medicine, Jinan University, Guangzhou 510632, China.
Protein Expr Purif. 2012 Mar;82(1):186-91. doi: 10.1016/j.pep.2012.01.002. Epub 2012 Jan 10.
Cofilin1 is an actin-binding protein that plays a critical role in the regulation of actin cytoskeleton and consequently affects various physiological processes. In this study, the human Cofilin1 cDNA was cloned into the expression vector pET-28a(+) with a 6 × His tag and expressed as soluble protein in Escherichia coli BL21(DE3). Approximately 78 mg of Cofilin1, which showed high activity as determined by native PAGE, could be purified from each liter of LB medium by His-tag affinity chromatography and gel filtration. Further, high-titer IgG against Cofilin1 was positively detected after immunization in rabbits and the polyclonal antibodies were purified and identified. Together, this report provides the first protocol to efficiently obtain human Cofilin1 with high biological activity and immunogenicity using E. coli BL21 (DE3) expression system.
丝切蛋白1是一种肌动蛋白结合蛋白,在肌动蛋白细胞骨架的调节中起关键作用,进而影响各种生理过程。在本研究中,将人丝切蛋白1 cDNA克隆到带有6×组氨酸标签的表达载体pET-28a(+)中,并在大肠杆菌BL21(DE3)中表达为可溶性蛋白。通过天然聚丙烯酰胺凝胶电泳测定,每升LB培养基经组氨酸标签亲和层析和凝胶过滤可纯化得到约78 mg具有高活性的丝切蛋白1。此外,兔免疫后阳性检测到高效价抗丝切蛋白1的IgG,并对多克隆抗体进行了纯化和鉴定。总之,本报告提供了首个使用大肠杆菌BL21(DE3)表达系统高效获得具有高生物活性和免疫原性的人丝切蛋白1的方案。