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首页> 外文期刊>Journal of Applied Polymer Science >Synthesis of lysozyme imprinted column with macroporous structure and enhanced selectivity: Utilization of cryogelation technique and electrostatic functional monomers
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Synthesis of lysozyme imprinted column with macroporous structure and enhanced selectivity: Utilization of cryogelation technique and electrostatic functional monomers

机译:大孔结构和选择性提高的溶菌酶印迹柱的合成:冷冻凝胶技术和静电功能单体的应用

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摘要

Applicability of molecularly imprinted polymers (MIP) in conventional protein separation processes demands monolithic construction of columns with macroporous structure in addition to the high specificity and adsorption capacity. In this study, therefore, lysozyme (Lyz) imprinted monolithic cryogel columns were synthesized using electrostatic functional monomers (EFMs) to provide strong interactions between template and polymer, leading to specific recognition and capture of Lyz. SEM images and FTIR spectroscopy analysis confirmed the macroporous structure and presence of EFMs in the samples. Adsorption isotherms, heterogeneity, and breakthrough curves as well as selectivity of the molecularly imprinted cryogels (EFMs-MIC) and non-imprinted cryogels (EFMs-NIC) were investigated. Results showed effective imprinting with a maximum adsorption capacity of 211 mg/g and a high imprinting factor (IF) of 4.2 at low Lyz concentrations. A high relative selectivity coefficient of 7.24 was obtained for Lyz over cytochrome c, a competing protein, indicating that the imprinted sites could well distinguish Lyz. Reusability of MICs was also examined, where insignificant changes were observed in the cryogel adsorption/desorption characteristics after four cycles. Therefore, it is suggested to use EFMs and cryogelation in the synthesis of imprinted monolithic cryogels column for application in conventional protein separation processes. (C) 2015 Wiley Periodicals, Inc.
机译:分子印迹聚合物(MIP)在常规蛋白质分离过程中的适用性要求具有高特异性和吸附能力的大分子结构色谱柱需要整体构建。因此,在这项研究中,使用静电功能单体(EFM)合成了溶菌酶(Lyz)印迹整体式冷冻凝胶柱,以提供模板与聚合物之间的强相互作用,从而导致对Lyz的特异性识别和捕获。 SEM图像和FTIR光谱分析证实了样品中的大孔结构和EFM的存在。研究了分子印迹冰晶(EFMs-MIC)和非印迹冰晶(EFMs-NIC)的吸附等温线,非均质性和穿透曲线以及选择性。结果显示有效的印迹,在低Lyz浓度下的最大吸附容量为211 mg / g,高印迹因子(IF)为4.2。 Lyz在竞争蛋白上较细胞色素c高7.24的相对选择性系数,表明印迹的位点可以很好地区分Lyz。还检查了MIC的可重复使用性,在四个循环后,观察到的冷冻凝胶吸附/解吸特性没有明显变化。因此,建议在常规的蛋白质分离方法中使用EFM和冷冻凝胶法合成印迹整体式冷冻凝胶色谱柱。 (C)2015年Wiley Periodicals,Inc.

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