河蟹铜诱导金属硫蛋白的金属结合特征揭示了其铜硫蛋白特性

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Protein expression and purification Pub Date : 2024-06-01 DOI:10.1016/j.pep.2024.106519
Huizhen Yang , Ziyan Zhao , Hongquan Li , Lan Wang
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引用次数: 0

摘要

河南褐马鸡表达两种金属诱导型金属硫蛋白(MT),即镉诱导型MT和铜诱导型MT(ShCuMT)。镉诱导金属硫蛋白的特征是镉硫酸盐金属硫蛋白。但 ShCuMT 是否是硫代铜离子 MT 尚不清楚。在本研究中,ShCuMT 在大肠杆菌中异源表达,并通过 Ni-NTA 柱和 superdex-75 柱纯化。并通过 DTNB 反应、圆二色光谱(CD)、等温微滴定(ITC)、电喷雾飞行质谱(ESI-TOF-MS)和基质辅助激光解吸电离飞行质谱(MALDI-TOF-MS)对其金属结合特征进行了评估。生物信息学分析表明,ShCuMT具有铜特异性MT的半胱氨酸-三重基序。ShCuMT 的表达和纯化表明,SUMO 标记作为 ShCuMT 的生产系统可获得较高的产量。ShCuMT 与金属离子结合的稳定性顺序为铜(Ⅰ)>镉(Ⅱ)>锌(Ⅱ)。CD 光谱表明,ShCuMT 与铜(Ⅰ)结合后呈现出紧密的硫醇金属簇结构。此外,Ni-NTA 柱亲和层析后没有出现可见的镍硫醇吸收。ITC 结果表明,Cu-ShCuMT 具有最佳的热力学构象和最高的铜化学计量数(Ⅰ)。总之,研究结果表明,SUMO融合系统是表达ShCuMT的一种稳健而廉价的方法,Ni-NTA柱对ShCuMT的金属结合没有影响,Cu(Ⅰ)被认为是其同源金属离子,ShCuMT具有典型的Cu-硫酸盐特征。本文所报道的ShCuMT的金属结合特征有助于阐明河南沙门氏菌中ShCuMT的结构-功能关系。
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Metal binding feature of copper‒induced metallothionein from freshwater crab Sinopotamon henanense reveals its Cu‒thionein character

Sinopotamon Henanense expresses two metal‒induced metallothioneins (MTs), Cd‒induced MT and Cu‒induced MT (ShCuMT). The Cd‒induced MT has been characterized as a Cd‒thiolate MT. However, it is unknown whether ShCuMT is a Cu‒thiolate MT. In the present study, ShCuMT was expressed heterologously in Escherichia coli and purified by Ni‒NTA column and superdex‒75 column. And its metal‒binding feature was evaluated by DTNB reaction, circular dichroism spectroscopy (CD), isothermal microtitration (ITC), electrospray flight mass spectrometry (ESI‒TOF‒MS), and matrix‒assisted laser desorption ionization flight mass spectrometry (MALDI‒TOF‒MS). Bioinformatics analysis demonstrated that ShCuMT possessed the cysteine‒triplet motif of a Cu‒specific MT. Expression and purification of ShCuMT illustrated that SUMO tag used as the production system for ShCuMT resulted in a high production yield. The stability order of ShCuMT binding metal ions were Cu (Ⅰ) > Cd (Ⅱ) > Zn (Ⅱ). The CD spectrum indicated that ShCuMT binding with Cu (I) exhibited a compact thiol metal clusters structure. Besides, there emerged no a visible nickel‒thiol absorption after Ni‒NTA column affinity chromatography. The ITC results implied that Cu‒ShCuMT possessed the optimal thermodynamic conformation and the highest stoichiometric number of Cu (Ⅰ). Overall, the results suggested that SUMO fusion system is a robust and inexpensive approach for ShCuMT expression and Ni‒NTA column had no influence on metal binding of ShCuMT and Cu(Ⅰ) was considered its cognate metal ion, and ShCuMT possessed canonical Cu‒thiolate characteristics. The metal binding feature of ShCuMT reported here contributes to elucidating the structure‒function relationship of ShCuMT in S. Henanense.

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来源期刊
Protein expression and purification
Protein expression and purification 生物-生化研究方法
CiteScore
3.70
自引率
6.20%
发文量
120
审稿时长
32 days
期刊介绍: Protein Expression and Purification is an international journal providing a forum for the dissemination of new information on protein expression, extraction, purification, characterization, and/or applications using conventional biochemical and/or modern molecular biological approaches and methods, which are of broad interest to the field. The journal does not typically publish repetitive examples of protein expression and purification involving standard, well-established, methods. However, exceptions might include studies on important and/or difficult to express and/or purify proteins and/or studies that include extensive protein characterization, which provide new, previously unpublished information.
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