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A poly(2-hydroxyethyl methacrylate)-based immobilized metal affinity chromatography adsorbent for protein purification

机译:一种基于聚(甲基丙烯酸2-羟乙酯)的固定化金属亲和色谱吸附剂,用于蛋白质纯化

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摘要

Poly(HEMA) microbeads were prepared by suspension polymerization of 2-hydorxyethylmethacrylate and ethyleneglycoldimethacrylate (EGDMA). The water content, ligand density, and selectivity for poly(His)-tagged D-hydantoinase of the poly(HEMA)-based adsorbents were affected by the concentration of EDGMA used during polymerization. The Ni(II)-loaded poly(HEMA) adsorbent exhibited an adsorption capacity of 1.0 mg/g for poly(His)-tagged D-hydantoinase under optimal conditions with buffer containing 100-300 mM NaCl at pH 6.0. One-step purification protocol with the adsorbent gave a purity of at least 92%. The adsorption capacity of adsorbent declined by 54% after 7 cycles, due to the leaching of Ni(11) from the adsorbent. However, upon regeneration the adsorption capacity can be restored. Given the ease of preparation and the chemical and microbial resistance, the poly (HEMA)-based IMAC adsorbent could be a promising substitute for the polysaccharide-based IMAC adsorbents. (c) 2008 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:聚(HEMA)微珠是通过甲基丙烯酸2-羟乙基酯与甲基丙烯酸乙二醇二乙酯(EGDMA)的悬浮聚合制备的。聚(HEMA)基吸附剂中聚(His)标记的D-乙内酰脲酶的水含量,配体密度和选择性受聚合过程中使用的EDGMA浓度的影响。负载Ni(II)的聚(HEMA)吸附剂在最佳条件下,在pH 6.0的缓冲液中含有100-300 mM NaCl时,对聚(His)标记的D-乙内酰脲酶的吸附能力为1.0 mg / g。用吸附剂进行的一步纯化方案得到的纯度至少为92%。 7个循环后,由于Ni(11)从吸附剂中浸出,吸附剂的吸附能力下降了54%。然而,再生后,吸附能力可以恢复。考虑到易于制备以及化学和微生物耐受性,基于聚(HEMA)的IMAC吸附剂可能是基于多糖的IMAC吸附剂的有希望的替代品。 (c)2008台湾化学工程师学会。由Elsevier B.V.发布。保留所有权利。

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