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Effect of His-Tag on Expression Purification and Structure of Zinc Finger Protein ZNF191(243-368)

机译:His-tag对锌指蛋白ZNF191(243-368)表达纯化和结构的影响

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摘要

Zinc finger proteins are associated with hereditary diseases and cancers. To obtain an adequate amount of zinc finger proteins for studying their properties, structure, and functions, many protein expression systems are used. ZNF191(243-368) is a zinc finger protein and can be fused with His-tag to generate fusion proteins such as His6-ZNF191(243-368) and ZNF191(243-368)-His8. The purification of His-tag protein using Ni-NTA resin can overcome the difficulty of ZNF191(243-368) separation caused by inclusion body formation. The influences of His-tag on ZNF191(243-368) properties and structure were investigated using spectrographic techniques and hydrolase experiment. Our findings suggest that insertion of a His-tag at the N-terminal or C-terminal end of ZNF191(243-368) has different effects on the protein. Therefore, an expression system should be considered based on the properties and structure of the protein. Furthermore, the hydrolase activity of ZNF191(243-368)-His8 has provided new insights into the design of biological functional molecules.
机译:锌指蛋白与遗传性疾病和癌症有关。为了获得足够量的锌指蛋白以研究其性质,结构和功能,使用了许多蛋白表达系统。 ZNF191(243-368)是锌指蛋白,可与His-tag融合以生成融合蛋白,例如His6-ZNF191(243-368)和ZNF191(243-368)-His8。用Ni-NTA树脂纯化His-tag蛋白可以克服包涵体形成引起的ZNF191(243-368)分离困难。利用光谱技术和水解酶实验研究了His标签对ZNF191(243-368)性质和结构的影响。我们的发现表明,在ZNF191(243-368)的N末端或C末端插入His标签会对蛋白质产生不同的影响。因此,应基于蛋白质的特性和结构来考虑表达系统。此外,ZNF191(243-368)-His8的水解酶活性为生物功能分子的设计提供了新的见识。

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