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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >A novel method for immobilization of proteins via entrapment of magnetic nanoparticles through epoxy cross-linking
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A novel method for immobilization of proteins via entrapment of magnetic nanoparticles through epoxy cross-linking

机译:通过环氧交联通过捕获磁性纳米粒子固定蛋白质的一种新方法

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A method for immobilization of functional proteins by chemical cross-linking of the protein of interest and uncoated iron oxide nanoparticles in the presence of Epichlorohydrin is described. As a result of the cross-linking, the proteins form a matrix in which the particles get entrapped. The optimum concentration of Epichlorohydrin that facilitates immobilization of protein without affecting the functional properties of the protein was determined. This method was used to immobilize several functional proteins and the development and functional activity of Protein A-magnetic nanoparticles (MNPs) is described here in detail. The Protein A-MNPs possess high binding capacity due to the increased surface area of uncoated nanoparticles and robust magnetic separation due to the absence of polymeric coating materials. Protein A-MNPs were successfully used for purification of antibodies and also for immunoprecipitation. We also immobilized enzymes such as horse radish peroxidase and esterase and found that by providing the optimum incubation time, temperature and protein to nanoparticle ratio, we can retain the activity and improve the stability of the enzyme. This study is the first demonstration that Epichlorohydrin can be used to entrap nanoparticles in a cross-linked matrix of protein without impairing the activity of immobilized protein. (C) 2016 Elsevier Inc. All rights reserved.
机译:描述了通过化学交联通过感兴趣的蛋白质和未涂层氧化铁纳米颗粒在表壳存在下的化学交联来固定功能蛋白质的方法。作为交联的结果,蛋白质形成粒子的基质,其中颗粒被捕获。测定了促进蛋白质的固定而不影响蛋白质的功能性质的促进蛋白质的最佳浓度。该方法用于固定几种功能性蛋白质,详细描述了蛋白质A-磁性纳米颗粒(MNP)的发育和功能活性。由于未涂覆的纳米颗粒的表面积增加,蛋白A-MNP具有高结合能力,并且由于不存在聚合物涂料而具有稳健的磁性分离。蛋白A-MNP已成功用于纯化抗体,也用于免疫沉淀。我们还固定诸如马萝卜过氧化物酶和酯酶等酶,并发现通过向纳米颗粒比提供最佳孵育时间,温度和蛋白质,我们可以保留活性并改善酶的稳定性。该研究是第一次证明,即环氯醇可用于在不损害固定蛋白的活性的情况下以交联蛋白质的交联基质中捕获纳米颗粒。 (c)2016年Elsevier Inc.保留所有权利。

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