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Polymer composition primarily determines the protein recognition characteristics of molecularly imprinted hydrogels

机译:聚合物组合物主要决定分子印迹水凝胶的蛋白质识别特征

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摘要

Synthetic hydrogels with the ability to recognize and bind target proteins are useful for a number of applications, including biosensing and therapeutic agent delivery. One popular method for fabricating recognitive hydrogels is molecular imprinting. A long-standing hypothesis of the field is that these molecularly imprinted polymers (MIPs) retain the chemical and geometric profile of their protein template, resulting in subsequent ability to recognize the template in solution. Here, we systematically determined the influence of network composition, as well as the identity, amount, and extraction of imprinting templates, on the protein binding of MIPs. Network composition (i.e.the relative number of ionizable and hydrophobic groups) explained the extent of protein adsorption in all cases. The identity and amount of imprinting template, albeit a protein or synthetic polymer (PEG) of similar molecular weight, did not significantly influence the amount of protein bound. While the purification method influenced the extent of template adsorption, it did so by chemically modifying the network (acrylamide hydrolysis, increasing the acid content by up to 21%) and not by voiding occupied MIP pores. Therefore, our results indicate that material composition determines the extent to which MIPs bind template and non-template proteins.
机译:具有识别和结合靶蛋白的能力的合成水凝胶可用于许多应用,包括生物传感和治疗剂递送。制造识别水凝胶的一种普遍的方法是分子印迹。该领域的长期假设是这些分子印迹聚合物(MIPS)保留了其蛋白质模板的化学和几何曲线,从而导致随后识别溶液中模板的能力。在这里,我们系统地确定了网络组成的影响,以及印迹模板的身份,量和提取,对MIP的蛋白质结合。网络组成(即电离和疏水基团的相对数量)解释了所有病例中蛋白质吸附的程度。印迹模板的身份和量,尽管类似分子量的蛋白质或合成聚合物(PEG),并未显着影响蛋白质结合的量。虽然纯化方法影响了模板吸附的程度,但它通过化学修饰网络(丙烯酰胺水解,将酸含量增加至多21%)而不是通过空隙占用的壁孔。因此,我们的结果表明,材料组合物决定了MIPS结合模板和非模板蛋白的程度。

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