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首页> 外文期刊>Analytical chemistry >Enhanced Lysozyme Imprinting Over Nanoparticles Functionalized with Carboxyl Groups for Noncovalent Template Sorption
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Enhanced Lysozyme Imprinting Over Nanoparticles Functionalized with Carboxyl Groups for Noncovalent Template Sorption

机译:增强的溶菌酶印迹在功能化羧基基团的非共价模板吸附纳米粒子上。

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摘要

Surface molecular imprinting, in particular over nanosized support materials, is very suitable for a template of bulky structure like protein. Inspired by the surface template immobilization method reported previously, we herein demonstrate an alternative strategy for enhancing specific recognition of core-shell protein-imprinted nanoparticles through pre-functionalizing the cores with noncovalent template sorption groups. For proof of this concept, silica nanoparticles chosen as the core materials were modified consecutively with 3-aminopropyltrimethoxysilane and maleic anhydride to introduce polymerizable double bonds and terminal carboxyl groups, hence capable of physically adsorbing the print protein. With lysozyme as a template, thin protein-imprinted shells were fabricated according to our newly developed approach for surface protein imprinting over nanoparticles. The rebinding experiments confirmed that the introduction of the carboxyl groups could remarkably improve the imprinting effect in relation to a significantly increased imprinting factor and specific rebinding capacity. Moreover, in contrast to the harsh template removal conditions required for the covalent template coupling approach, the template removal during the imprinted particle synthesis as well as desorption after rebinding could be mildly achieved via washing with salt solution.
机译:表面分子印迹,特别是在纳米级载体材料上的印迹,非常适合像蛋白质这样的大结构模板。受先前报道的表面模板固定方法的启发,我们在本文中演示了通过使用非共价模板吸附基团对核进行预功能化来增强对核-壳蛋白印迹纳米颗粒的特异性识别的替代策略。为了证明这一概念,选择了用作核心材料的二氧化硅纳米粒子,分别用3-氨丙基三甲氧基硅烷和马来酸酐进行改性,以引入可聚合的双键和末端羧基,从而能够物理吸附印刷蛋白质。以溶菌酶为模板,根据我们新开发的表面蛋白印迹在纳米颗粒上的方法,制备了薄蛋白印迹的外壳。结合实验证实,与显着增加的印迹因子和比结合能力相比,引入羧基可以显着改善印迹效果。而且,与共价模板偶联方法所要求的苛刻的模板去除条件相反,可以通过用盐溶液洗涤温和地实现印迹颗粒合成过程中的模板去除以及重新结合后的脱附。

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