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Silica-based surface molecular imprinting for recognition and separation of lysozymes

机译:基于硅胶的表面分子印迹技术,用于溶菌酶的识别和分离

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A highly selective surface molecularly imprinted inorganic polymer composed of tetraethoxysilane and 3-aminopropyltriethoxysilane has been prepared by a sola€“gel process on silica submicroparticles in aqueous solution under simple and mild conditions. Lysozyme (Lyz, pI 11, MW 14.4 kDa) is used as the template protein. The product polymers were characterized by FT-IR, TEM, and TG techniques to verify the successful synthesis of the MIP on the surface of silica submicroparticles. The adsorption behavior of the MIP was evaluated by adsorption capacity, imprinting factor and adsorption model. It was found that both MIP and NIP could adsorb the template protein quickly and easily owing to the low mass transfer resistance of the thin shell and their adsorption equilibrium could be reached in 5 h. Compared with the NIP, the MIP showed stronger adsorption capacity for template protein Lyz under all experimental conditions. The mechanism for static adsorption of Lyz onto the MIP was found to follow the Langmuir adsorption model which was further used to calculate the maximum adsorption capacity Qmax and gave a result of 90.33 mg ga?’1 in theory. The MIP adsorbent could be reused twice without significant loss in adsorption capacity. The MIP indicated excellent recognition and binding affinity toward Lyz, whose selectivity factor ?2 for Lyz relative to reference proteins bovine serum albumin (BSA, pI 4.9, MW 69.0 kDa), bovine hemoglobin (BHb, pI 6.9, MW 65.0 kDa) and ovalbumin (OVA, pI 4.7, MW 43.0 kDa) were 2.36, 2.22, and 2.24, respectively. It was shown that the shape memory and the size effect were the major factors for the recognition. This imprinted inorganic polymer was used to specifically adsorb the Lyz from the protein mixture, which demonstrated its potential selectivity.
机译:在简单,温和的条件下,通过溶胶凝胶法在水溶液中的二氧化硅亚微粒上制备了由四乙氧基硅烷和3-氨基丙基三乙氧基硅烷组成的高选择性表面分子印迹无机聚合物。溶菌酶(Lyz,pI 11,MW 14.4kDa)用作模板蛋白。通过FT-IR,TEM和TG技术对产物聚合物进行表征,以验证二氧化硅亚微粒表面MIP的成功合成。通过吸附容量,印迹因子和吸附模型评价了MIP的吸附行为。结果发现,由于薄壳的传质阻力小,MIP和NIP都能快速,轻松地吸附模板蛋白,并在5 h内达到吸附平衡。与NIP相比,MIP在所有实验条件下对模板蛋白Lyz的吸附能力均强。发现将Lyz静态吸附在MIP上的机理遵循Langmuir吸附模型,该模型进一步用于计算最大吸附容量Qmax,理论上得出的结果为90.33 mg ga?-1。 MIP吸附剂可以重复使用两次,而不会显着降低吸附能力。 MIP显示出对Lyz的出色识别和结合亲和力,相对于参考蛋白牛血清白蛋白(BSA,pI 4.9,MW 69.0 kDa),牛血红蛋白(BHb,pI 6.9,MW 65.0 kDa)和卵清蛋白,Lyz的选择性因子α2。 (OVA,pI 4.7,MW 43.0 kDa)分别为2.36、2.22和2.24。结果表明,形状记忆和尺寸效应是识别的主要因素。这种印迹的无机聚合物用于从蛋白质混合物中特异性吸附Lyz,这证明了其潜在的选择性。

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