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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
Institution:1. Department of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China;2. State Key Laboratory of Chemical Engineering, Institute of Polymerization and Polymer Engineering, Zhejiang University, Hangzhou 310027, China;1. Department of Psychiatry and Behavioral Health, The Ohio State University, Columbus, OH, USA;2. Department of Psychology, The Ohio State University, Columbus, OH, USA;1. Dr Stanislaw Sakiel Centre for Burn Treatment, Siemianowice Śląskie, Poland;2. School of Health Sciences of the University, Bielsko Biała, Poland;3. Centre of Polymer and Carbon Materials, Polish Academy of Sciences, Zabrze, Poland;4. Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Łódź, Poland;1. Department of Materials Science and Technology, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan;2. The OCU Advanced Research Institute for Natural Science and Technology, Osaka City University, 3-3-138 Sugimotocho, Sumiyoshi-ku, Osaka, Osaka 558-8585, Japan
Abstract:Recombinant human interferon gamma (rhIFN-γ) is a protein with great potential for clinical therapy, but rhIFN-γ 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-γ 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-γ refolding which presented an alternative way to facilitate recombinant protein refolding in vitro.
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