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首页> 外文期刊>Biochemical Engineering Journal >Refolding of recombinant human interferon gamma inclusion bodies in vitro assisted by colloidal thermo-sensitive poly(N-isopropylacrylamide) brushes grafted onto the surface of uniform polystyrene cores
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Refolding of recombinant human interferon gamma inclusion bodies in vitro assisted by colloidal thermo-sensitive poly(N-isopropylacrylamide) brushes grafted onto the surface of uniform polystyrene cores

机译:胶体热敏聚(N-异丙基丙烯酰胺)毛笔移植到均一聚苯乙烯核表面上,协助重组人干扰素γ体外重组体折叠

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摘要

Recombinant human interferon gamma (rhIFN-7) is a protein with great potential for clinical therapy, but rhIFN--y expressed in Escherichia coli is usually in the form of insoluble inclusion bodies which should be refolded in vitro. A novel type of hairy particles (PNIPAM-grafted-PS) consisted of submicron polystyrene cores and brushes of thermo-sensitive poly(N-isopropylacrylamide) grafted onto the cores was prepared and then applied to assist the refolding of rhIFN-7 in vitro. Two kinds of PNIPAM-grafted-PS particles with different thickness of brush layer (55 nm and 110 nm) were synthesized, which were spherical shape with good dispersion properties and the LCST was about 33 °C. The effect of thickness of brush layer, particle concentration and temperature on the refolding process was investigated, it was shown that particles with larger thickness of brush layer were more effective and the final rhIFN-γ activity could be up to more than 21 times of that in dilution refolding when initial rhIFN-γ concentration was 50 μg/mL The optimal refolding condition was the concentration ratio of particle to rhIFN-γ 1:1 and refolding temperature of 15 °C. All results above demonstrated that PNIPAM-grafted-PS particles could assist rhIFN-7 refolding which presented an alternative way to facilitate recombinant protein refolding in vitro.
机译:重组人干扰素γ(rhIFN-7)是一种具有巨大临床潜力的蛋白质,但在大肠杆菌中表达的rhIFN-y通常为不溶性包涵体,应在体外重新折叠。制备了一种由亚微米聚苯乙烯核组成的新型毛状颗粒(PNIPAM-嫁接的PS),并制备了接枝到核上的热敏性聚(N-异丙基丙烯酰胺)刷,然后用于协助重组rhIFN-7在体外。合成了两种不同刷层厚度(55 nm和110 nm)的PNIPAM接枝PS颗粒,它们均为球形,具有良好的分散性,LCST约为33°C。研究了刷层厚度,颗粒浓度和温度对复性过程的影响,结果表明,刷层厚度较大的颗粒更有效,最终rhIFN-γ活性可达其的21倍以上。 rhIFN-γ初始浓度为50μg/ mL时稀释复性的最佳复性条件为颗粒与rhIFN-γ的浓度比为1:1,复性温度为15°C。以上所有结果表明,PNIPAM接枝的PS颗粒可协助rhIFN-7重折叠,为体外重组蛋白重折叠提供了另一种方法。

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