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Chin. J. Process Eng. ›› 2017, Vol. 17 ›› Issue (4): 834-838.DOI: 10.12034/j.issn.1009-606X.216364

• Biochemical Engineering • Previous Articles     Next Articles

Expression, Purification and Crystallization of Inactivated Serine Protease Domain of Matriptase

Tuanyu GUO1,3,  Baoyu ZHAO2,  Cai YUAN2*,  Mingdong HUANG2   

  1. 1. Department of Biology, Ningde Normal University, Ningde, Fujian 352100, China; 
    2. Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China; 
    3. Fujian Provincial Key Laboratory of Featured Materials in Biochemical Industry, Ningde 352100, China
  • Received:2016-12-05 Revised:2017-01-14 Online:2017-08-20 Published:2017-08-16

丝氨酸蛋白酶催化结构域无活性突变体的表达、纯化与结晶

郭团玉1,3， 赵宝玉2， 袁 彩2*， 黄明东2   

  1. 1. 宁德师范学院生物系，福建 宁德 352100；2. 中国科学院福建物质结构研究所，福建 福州 350007； 3. 特色生物化工材料福建省重点实验室，福建 宁德 352100
  • 通讯作者: 袁彩 cyuan@fzu.edu.cn
  • 基金资助:
    国家自然科学基金

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Abstract: An inactivated mutant of matriptase serine protease domain (S195A) was constructed, and the recombinant protein in Pichia pastoris was expressed. After captured by anion exchange chromatography, the recombinant protein was further purified by gel-filtration chromatogram column and resource Q anion exchange column with high purity. High quality crystals of this inactivated protein were obtained by sitting-drop vapor diffusion. The results showed that the single point mutant increased the level of matriptase compared with the wild type. This inactivated mutant forms stable complex with its inhibitor HAI-1, although it does not possess catalytic activity. Crystals of this inactivated protein were diffracted to 1.48 ?. The mutant has the same conformation as the wild type.

Key words: matriptase, crystal growth

摘要： 构建了丝氨酸蛋白酶Matriptase的催化结构域无活性突变体质粒S195A，并在酵母中表达，通过阴离子柱粗捕获及分子筛和离子交换柱纯化得到高纯度重组蛋白，通过气相扩散法得到无活性突变体的晶体. 结果表明，与野生型相比，单点突变极大程度提高了Matriptase的表达，Matriptase无活性突变体不具有水解底物活性，但仍可与抑制蛋白HAI-1结合. 晶体分辨率为1.48 ?，195A突变没有影响Matriptase的构象.

关键词: 丝氨酸蛋白酶, 表达, 晶体生长