Expression, purification, and characterization of N-terminal His-tagged proteins with mutations in zinc finger 3 of zinc finger protein ZNF191(243-368)

被引:2
|
作者
Zhao, Dongxin [1 ]
Huang, Zhongxian [2 ]
Liu, Jie [1 ]
Ma, Li [1 ]
He, Juan [1 ]
机构
[1] Henan Univ Technol, Coll Chem Chem & Environm Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Fudan Univ, Dept Chem, Shanghai, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Artificial nuclease; coordination; His tag; hydrolysis; mutant; zinc finger protein; BINDING; DNA; SEQUENCE; FLUORESCENCE; TRYPTOPHAN; CLEAVAGE; TYROSINE; PEPTIDE;
D O I
10.1080/10826068.2018.1514518
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Zinc finger protein ZNF191(243-368), the zinc finger region of ZNF191, is potentially associated with cell proliferation in hepatocellular carninoma. A His-tag expression system was used to express and purify proteins with mutations in the zinc finger 3 of ZNF191(243-368) for analysis of protein properties, structure, and functions. The purification of the His-tag fusion proteins was simpler and faster than that of the ZNF191(243-368) inclusion bodies. The properties and structures of the His-tag fusion mutant proteins were investigated using spectrographic techniques and DNA hydrolysis experiment. The His(6)-tag system could be used to express ZNF191(243-368). The presence of the His(6)-tag at the N-terminus of ZNF191(243-368) did not evidently affect its properties and structure. However, the site-directed mutations in zinc finger 3 affected the structure of the protein. The DNA hydrolase activity of His(6)-ZF-F3/H4 suggested that four histidines in zinc finger 3 might form a structure similar to that of the active center in a hydrolase. This work reports that continuous histidines need to form a certain structure for specific functions, and provides new insights into the design of an artificial nuclease.
引用
收藏
页码:914 / 919
页数:6
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