|本期目录/Table of Contents|

[1]牛 健,于晓旭,李 雪,等.重组 CARDs TX 融合蛋白的表达纯化与复性[J].天津医科大学学报,2014,20(03):184-187.
 NIU Jian,YU Xiao-xu,LI Xue,et al.Expression, purification and renaturation of recombinant CARDs TX fusion protein[J].Journal of Tianjin Medical University,2014,20(03):184-187.
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重组 CARDs TX 融合蛋白的表达纯化与复性(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
20
期数:
2014年03期
页码:
184-187
栏目:
基础医学
出版日期:
2014-05-20

文章信息/Info

Title:
Expression, purification and renaturation of recombinant CARDs TX fusion protein
文章编号:
1006-8147(2014)03-0184-04
作者:
牛 健于晓旭李 雪鲍会静刘运德
(天津医科大学医学检验学院, 天津 300203)
Author(s):
NIU Jian YU Xiao-xu LI Xue BAO Hui-jing LIU Yun-de
(School of Medical Laboratory, Tianjin Medical University, Tianjin 300203, China)
关键词:
 CARDs TX质粒构建点突变蛋白纯化蛋白复性
Keywords:
CARDs TX plasmid construction point mutation protein purification protein renaturation
分类号:
-
DOI:
-
文献标志码:
A
摘要:
目的:构建 pET28α-CARDs TX 重组质粒,诱导 CARDs TX 融合蛋白表达,并对其进行纯化与复性研究。方法:将 CARDs TX 基因(MPN 372)克隆入 pET28α 载体,经 8 次点突变获得 pET28α-CARDs TX 重组质粒。转化大肠杆菌 BL21,IPTG 诱导表达。利用亲和层析技术纯化蛋白并通过 SDS-PAGE 和 Wetern Blot 检测 CARDs TX 的表达和纯化效果。利用尿素梯度复性法和扩大体积透析法对蛋白进行复性研究。结果:酶切和测序结果证明 pET28α-CARDs TX 重组质粒的 DNA 序列完全正确,在 BL21 中 CARDs TX 融合蛋白可高效表达,并可获得高纯度目的蛋白。利用扩大体积透析法对目的蛋白复性有较好的效果。 结论:成功构建出 pET28α-CARDs TX 重组质粒,且 CARDs TX 可在大肠杆菌中高效表达,并可获得高纯度的目的蛋白,为深入研究 CARDs TX 的生物学特性奠定了基础。
Abstract:
Objective: To obtain recombinant CARDs TX fusion protein from BL21 cells. Methods: The CARDs TX gene (MPN 372) was cloned into vector pET28α and the integral CARDs TX expression vector was obtained after single gene point-mutations. The constructed recombinant plasmid was transformed into E.coli BL21 for expression under induction of IPTG. The Ni-NTA was used to purify the CARDs TX and the urea was desalted to get the refolding protein. Results: Enzyme digestion and gene sequencing analysis showed that pET28α-CARDs TX recombinant plasmid DNA sequences were completely correct. CARDs TX fusion protein can be expressed efficiently in BL21 and high purity target protein could be obtained. Expanded volume dialysis method applied had significant positive effect on the renaturation of the target protein. Conclusion: To successfully purify the CARDs TX and construct the CARDs TX expression vector that can be efficiently expressed in E. Coli.

参考文献/References:

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备注/Memo

备注/Memo:
作者简介 牛健(1989-),男,硕士在读,研究方向:临床检验诊断学;通信作者:刘运德,E-mail:yundeliu@126.com;鲍会静,E-mail:kris_10713@126.com
更新日期/Last Update: 2014-05-12