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Increased Protein Sorption in Poly(acrylic acid)-Containing Films Through Incorporation of Comb-like Polymers and Film Adsorption at Low pH and High Ionic Strength

机译:增加的蛋白质吸附在聚(丙烯酸)的膜通过掺入梳状聚合物和薄膜吸附在低pH和高离子强度

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摘要

In principle, incorporation of comb-like block copolymers in multilayer polyelectrolyte films can both increase film thickness relative to coatings containing linear polymers and provide more swollen films for increased sorption of proteins. In the absence of added salt, alternating adsorption of 5 bilayers of protonated poly(allylamine) (PAH) and comb-like poly(2-hydroxyethyl methacrylate)-graft-poly(acrylic acid) (PHEMA-g-PAA) leads to ∼2-fold thicker coatings than adsorption of PAH and linear PAA, and the difference in the thicknesses of the two coatings increases with the number of bilayers. Moreover, the (PAH/PHEMA-g-PAA)n films sorb 2- to 4-fold more protein than corresponding films prepared with linear PAA, and coatings deposited at pH 3.0 sorb more protein than coatings adsorbed at pH 5.0, 7.0, or 9.0. In fact changes in deposition pH and addition of 0.5 M NaCl to polyelectrolyte adsorption solutions alter protein sorption more dramatically than variations in the constituent polymer architecture. When deposited from 0.5 M NaCl at pH 3, both (PAH/PHEMA-g-PAA)5 and (PAH/PAA)5 films increase in thickness more than 400% upon adsorption of lysozyme. These films contain a high concentration of free –COOH groups, and subsequent deprotonation of these groups at neutral pH likely contributes to increased protein binding. Lysozyme sorption stabilizes these films, as without lysozyme films deposited at pH 3 from 0.5 M NaCl desorb at neutral pH. Films deposited at pH 9 from 0.5 M NaCl are more stable and also bind large amounts of lysozyme. The high binding capacities of these films make them attractive for potential applications in protein isolation or immobilization of enzymes.
机译:原则上,在多层聚电解质膜中掺入梳状嵌段共聚物既可以相对于含有线性聚合物的涂层增加膜厚度,又可以提供更溶胀的膜以增加蛋白质的吸收。在没有添加盐的情况下,质子化的聚(烯丙胺)(PAH)和梳状聚(甲基丙烯酸2-羟乙酯)-接枝聚(丙烯酸)(PHEMA-g-PAA)的5个双层交替吸附导致〜涂层的厚度比PAH和线性PAA的吸附厚度大2倍,并且两个涂层的厚度差随着双层数的增加而增加。而且,(PAH / PHEMA-g-PAA)n膜的蛋白质吸附量比线性PAA制备的相应膜高2至4倍,并且在pH 3.0的条件下沉积的涂层比在pH 5.0、7.0或pH值下的涂层吸收的蛋白质更多9.0。实际上,沉积pH的变化以及向聚电解质吸附溶液中添加0.5 M NaCl的影响,与组成聚合物结构的变化相比,对蛋白质的吸附作用要大得多。当从pH值为3的0.5 M NaCl中沉积时,(PAH / PHEMA-g-PAA)5和(PAH / PAA)5膜在吸附溶菌酶后厚度增加超过400%。这些薄膜包含高浓度的游离–COOH基团,随后这些基团在中性pH下的去质子化可能有助于增加蛋白质结合。溶菌酶的吸附使这些膜稳定,因为没有pH值为0.5的0.5 M NaCl在中性pH上解吸的溶菌酶膜。由0.5 M NaCl在pH 9下沉积的薄膜更加稳定,并且还结合了大量的溶菌酶。这些薄膜的高结合能力使其对蛋白质分离或酶固定方面的潜在应用具有吸引力。

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