文章摘要
徐永江,柳学周,张 凯,武宁宁,刘芝亮,李春广.半滑舌鳎(Cynoglossus semilaevis Günther)IGF-Ⅱ的体外重组表达.渔业科学进展,2015,36(4):51-56
半滑舌鳎(Cynoglossus semilaevis Günther)IGF-Ⅱ的体外重组表达
In vitro Recombinant Expression of Insulin-Like Factor Ⅱfrom Cynoglossus semilaevis Günther
投稿时间:2014-04-16  修订日期:2014-06-17
DOI:10.11758/yykxjz.20150407
中文关键词: 半滑舌鳎  IGF-Ⅱ  原核表达  生物活性
英文关键词: Cynoglossus semilaevis Günther  IGF-Ⅱ  Prokaryotic expression  Bioactivity
基金项目:鲆鲽类现代产业技术体系(CARS-50)、山东省自然科学基金项目(ZR2012CQ025)、中央级公益性事业单位基本科研业务费项目(20603022012022)和绍兴市院校科技合作项目(2012704)共同资助
作者单位
徐永江 农业部海洋渔业可持续发展重点实验室 中国水产科学研究院黄海水产研究所 青岛 266071 
柳学周 农业部海洋渔业可持续发展重点实验室 中国水产科学研究院黄海水产研究所 青岛 266072 
张 凯 青岛贝宝海洋科技有限公司 青岛 266400
 
武宁宁 青岛市海洋与渔业局渔业技术推广站 青岛 266071 
刘芝亮 农业部海洋渔业可持续发展重点实验室 中国水产科学研究院黄海水产研究所 青岛 266075 
李春广 绍兴市鸿港农业开发有限公司 绍兴 312000 
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中文摘要:
      为在蛋白水平认识半滑舌鳎类胰岛素生长因子Ⅱ(IGF-Ⅱ)的生理功能,将IGF-Ⅱ成熟肽序列克隆到原核表达载体pET-28a中,成功构建了重组半滑舌鳎IGF-Ⅱ/pET28a质粒,导入到E. coli BL21(DE3)菌株后经IPTG诱导,获得了大小为11.4 kDa的重组IGF-Ⅱ蛋白,N端含6个组氨酸,可特异性地被6×His抗体识别。重组IGF-Ⅱ蛋白在最优诱导条件37℃诱导2 h,目的蛋白表达量占重组表达菌总蛋白的43.7%,重组蛋白主要以包涵体存在。将获得的重组蛋白包涵体经变性、纯化和复性后,获得了纯化的IGF-Ⅱ重组蛋白,其可在体外显著促进人乳腺癌MDA231细胞的增殖,表明IGF-Ⅱ重组蛋白具有体外细胞水平的生物活性。本研究结果可为认识鱼类IGF-Ⅱ生理功能及半滑舌鳎生长调控机制提供理论支撑。
英文摘要:
      To explore the role of insulin-like factor Ⅱ(IGF-Ⅱ) in growth regulation of Cynoglossus semilaevis Günther, the IGF-Ⅱ gene was expressed in vitro and the bioactivity was determined by methyl thiazolyl tetrazolium (MTT method). The mature peptide domain of IGF-Ⅱ gene of C. semilaevis Günther was cloned by PCR amplification and sequenced for verification. The obtained mature peptide fragment was then subcloned into the prokaryotic expression vector pET-28a (IGF-Ⅱ/pET28a). The recombinant plasmid was expressed in E.coli BL21 (DE3) cells and the recombinant IGF-Ⅱ protein containing 6×His tag at N-terminus was induced by IPTG. SDS-PAGE analysis indicated that the obtained IGF-Ⅱ protein was found in the form of inclusion bodies with molecular weight of 11.4 kDa, which accounted for 43.7% of the whole bacterial protein post 2-hour induction with IPTG. Western blotting analysis indicated that the recombinant IGF-Ⅱ protein had the antigenicity to 6×His antibody. The inclusion bodies containing recombinant protein were denaturalized, purified and annealed. The recombinant IGF-Ⅱ protein significantly promoted the proliferation of human breast cancer cells MDA231. Results could provide basic information on the role of IGF-Ⅱ in fish and be helpful to better understand the endocrine mechanism of sex-based dimorphic growth performance of C. semilaevis Günther.
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