›› 2015, Vol. 42 ›› Issue (5): 1069-1075.doi: 10.16431/j.cnki.1671-7236.2015.05.005

• 生物技术 • 上一篇    下一篇

小鼠骨桥蛋白的原核表达及多克隆抗体的制备与鉴定

刘祥, 陈春琳, 王杨科, 俱雄, 吴三桥, 张涛   

  1. 陕西理工学院生物科学与工程学院, 汉中 723001
  • 收稿日期:2014-11-12 出版日期:2015-05-20 发布日期:2015-06-02
  • 通讯作者: 刘祥 E-mail:liuxiang888525@163.com
  • 作者简介:刘祥(1983-),男,安徽合肥人,博士,硕士生导师,研究方向:蛋白质组学与免疫学
  • 基金资助:
    陕西省教育厅科学研究计划项目(2013JK0723);陕西理工学院人才启动项目(SLGQD13-15)

Prokaryotic Expression,Polyclonal Antibody Preparation and Identification of Mouse Osteopontin Protein

LIU Xiang, CHEN Chun-lin, WANG Yang-ke, JU Xiong, WU San-qiao, ZHANG Tao   

  1. College of Biological Sciences and Engineering, Shaanxi University of Technology, Hanzhong 723001, China
  • Received:2014-11-12 Online:2015-05-20 Published:2015-06-02

摘要: 为探索骨桥蛋白(OPN)调控骨代谢及与肿瘤的关系,本试验利用DNAMAN与Mega 5.02软件分析OPN蛋白系统进化关系;采用RT-PCR与分子克隆方法制备OPN蛋白表达载体;利用SDS-PAGE电泳切胶纯化、尿素浓度梯度复性获得OPN蛋白,免疫小鼠制备OPN蛋白多克隆抗体;采用ELISA法检测抗体滴度,Western blotting检测抗血清特异性。OPN序列的同源性比对分析发现,在不同进化层次动物中均存在Arg-Gly-Asp(RGD)短肽重复序列;OPN序列系统进化分析显示,OPN在动物间具有明显的进化趋势;提取小鼠肝脏RNA,OPN重组载体双酶切、DNA测序鉴定结果及蛋白表达、纯化条带大小均与预测一致;ELISA法确认OPN抗血清滴度达1:1 600;Western blotting证实抗血清具有很好的特异性。结果表明本试验对OPN序列进行了遗传进化分析,成功克隆、表达、纯化及复性OPN蛋白,并制备、鉴定了小鼠多克隆抗体。

关键词: OPN蛋白; RT-PCR; 多克隆抗体; ELISA; Western blotting

Abstract: In order to explore the function of osteopontin (OPN) regulated bone metabolism and the relationship between OPN and tumor, DNAMAN and Mega 5.02 softwares were used to analyze phylogenetic relationships of OPN protein, the OPN expression vector was prepared by RT-PCR and molecular clone; OPN was purified by SDS-PAGE gel slices, renatured by urea concentration gradient, and immunized mice to prepare the polyclonal antibody; The antibody titer and specificity were detected by ELISA and Western blotting, respectively.The homology comparison result of OPN sequence showed that it existed short repeat sequenc Arg-Gly-Asp (RGD) in different animals with evolution levels.Phylogenetic tree of OPN sequence showed that OPN had obvious evolution trend among animals.RNA was extracted, OPN recombinant vector had been digested and sequenced to confirm the correct construction, and strip lengths of OPN expression and purification were agreed with the prediction.The OPN antiserum titer was 1:1 600 detected by ELISA, and Western blotting proved that the antiserum had good specificity.We had successfully analyzed genetic evolution relationship of OPN sequence, gotten OPN expression vector, purified and renatured OPN, and prepared and identified the polyclonal antibody against OPN.

Key words: OPN protein; RT-PCR; polyclonal antibody; ELISA; Western blotting

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