Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto, 615-8510, Japan.
Department of Chemistry, Faculty of Science, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
J Mater Chem B. 2022 Sep 15;10(35):6800-6807. doi: 10.1039/d2tb00501h.
Protein imprinted hydrogel, which is one form of protein imprinted molecularly imprinted polymer (MIP), is an important material for enzyme-linked immunosorbent assay, drug delivery materials, sensors, separation materials, To obtain a high protein recognition performance, it is essential to optimize the involved compositions. This work studies a (poly(ethylene glycol) diacrylate/poly(ethylene glycol) acrylate), in short (PEGDA/PEGA), based MIP hydrogel targeting cytochrome recognition. The presented MIP hydrogel employs water-soluble PEGDA as the crosslinker, PEGA as the side chain, and sodium allylsulfonate as the functional monomer. The fabricated MIP hydrogels and non-imprinted polymer (NIP) hydrogels were treated as adsorbents for protein adsorption. Efforts were made targeting an optimized recognition performance. Factors including the template to functional monomer ratio, crosslinker length, crosslinker ratio of PEGDA/PEGA, ionic strength in the adsorption test, and presence of acidic modifier in the adsorption test were investigated. The results showed that a higher template to functional monomer ratio, a shorter crosslinker, and additional NaCl (20 mM) in the adsorption solvent provided a higher imprinting factor. A lower crosslinker ratio of no less than 6/4 offered a faster template removal; at the same time, the imprinting factor remained at a quite high level. Highly specific recognition of cytochrome was realized with the presence of an optimized amount of HCl (10 mM) as an acidic modifier.
蛋白质印迹水凝胶,作为蛋白质印迹分子印迹聚合物(MIP)的一种形式,是酶联免疫吸附测定、药物输送材料、传感器、分离材料等领域的重要材料。为了获得高的蛋白质识别性能,优化涉及的组成是必不可少的。本工作研究了一种(聚乙二醇二丙烯酸酯/聚乙二醇丙烯酸酯),简称(PEGDA/PEGA),基于靶向细胞色素识别的 MIP 水凝胶。所制备的 MIP 水凝胶和非印迹聚合物(NIP)水凝胶被用作蛋白质吸附的吸附剂,以优化识别性能。研究了包括模板与功能单体比、交联剂长度、PEGDA/PEGA 交联剂比、吸附试验中的离子强度以及吸附试验中存在酸性调节剂等因素。结果表明,较高的模板与功能单体比、较短的交联剂以及在吸附溶剂中添加 20mM 的 NaCl 提供了更高的印迹因子。交联剂比不低于 6/4 可提供更快的模板去除,同时印迹因子仍保持在相当高的水平。在存在优化量的 10mM HCl 作为酸性调节剂的情况下,实现了对细胞色素的高度特异性识别。