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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >One-step separation of the recombinant protein by using the amine-functionalized magnetic mesoporous silica nanoparticles; an efficient and facile approach
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One-step separation of the recombinant protein by using the amine-functionalized magnetic mesoporous silica nanoparticles; an efficient and facile approach

机译:通过使用胺官能化的磁性介孔二氧化硅纳米颗粒一步分离重组蛋白; 有效和轻松的方法

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The separation process is the main stage of recombinant production. With the advancement of nanotechnology and the development of magnetic nanoparticles, these structures are increasingly used in different applications. In the present study, we produced the recombinant human growth hormone from Pichia pastoris and for protein separation provided the surfaces similar to chromatographic columns on the surface of magnetic nanoparticles. For this purpose, using a co-precipitation method, the core of Fe3O4 was prepared and coated by silica. To increase the protein availability, silica mesoporous formation and its amine functionalization were performed. The specific surface area and the pore size were determined 78.3189 m(2)/g and 7.44 nm. After the magnetic separation, the sample loading in SDS gel shows a reduction in protein band and the protein absorption at a wavelength of 280 nm. Finally, we evaluate the ability of amine functionalized nanoparticles for protein separation that demonstrate the adsorption capacity significantly increased compare with silica-coated nanoparticles. The amine functionalized nanoparticles provide the maximum adsorption capacity of 235.21 mu g/mg and after the elution, protein concentration determined 476 mg/L. This work indicates the functionalized magnetic mesoporous silica nano particles can be used as the best candidate for the separation of different biological macromolecules. (C) 2019 Elsevier B.V. All rights reserved.
机译:分离过程是重组生产的主要阶段。随着纳米技术的进步和磁性纳米颗粒的发展,这些结构越来越多地用于不同的应用。在本研究中,我们生产来自Pichia Pastoris的重组人生长激素,并且蛋白质分离提供了与磁性纳米颗粒表面上的色谱柱类似的表面。为此目的,使用共析出方法,制备Fe3O4的核心并通过二氧化硅涂覆。为了提高蛋白质可用性,进行二氧化硅介孔形成及其胺官能化。测定比表面积和孔径为78.3189m(2)/ g和7.44nm。磁性分离后,SDS凝胶中的样品负载显示蛋白质带的还原和在280nm的波长下的蛋白质吸收。最后,我们评估胺官能化纳米颗粒用于蛋白质分离的能力,证明吸附能力明显增加与二氧化硅涂覆的纳米颗粒相比。胺官能化纳米颗粒提供235.21μg/ mg的最大吸附能力,洗脱后,蛋白质浓度测定476mg / L.该工作表明官能化磁性介孔二氧化硅纳米颗粒可用作分离不同生物大分子的最佳候选者。 (c)2019 Elsevier B.v.保留所有权利。

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