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Mixed Polymer Brushes for the Selective Capture and Release of Proteins

机译:混合聚合物刷,用于选择性捕获和释放蛋白质

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Selective protein adsorption is a key challenge for the development of biosensors, separation technologies, and smart materials for medicine and biotechnologies. In this work, a strategy was developed for selective proteidadsorption, based on the use of mixed polymer brushes composed of poly(ethylene oxide) (PEO), a protein-repellent polymer, and poly(acrylic acid) (PAA), a weak polyacid whose conformation changes according to the pH and ionic strength of the surrounding medium. A mixture of lysozyme (Lyz), human serum albumin (HSA), and human fibrinogen (Fb) was used to demonstrate the success of this strategy. Polymer brush formation and protein adsorption were monitored by quartz crystal microbalance, whereas protein identification after adsorption from the mixture was performed by time-of-flight secondary ion mass spectrometry (ToF-SIMS) with principal component analysis and gel electrophoresis with silver staining. For the ToF-SIMS measurements, adsorption was first performed from single-protein solutions in order to identify characteristic peaks of each protein. Next, adsorption was performed from the mixture of the three proteins. Proteins were also desorbed from the brushes and analyzed by gel electrophoresis with silver staining for further identification. Selective adsorption of Lyz from a mixture of Lyz/HSA/Fb was successfully achieved at pH 9.0 and ionic strength of 10(-3) M, while Lyz and HSA, but not Fb, were adsorbed at ionic strength 10(-2) M and pH 9.0. The results demonstrate that by controlling the ionic strength, selective adsorption can be achieved from protein mixtures on PEO/PAA mixed brushes, predominantly because of the resulting control on electrostatic interactions. In well-chosen conditions, the selectively adsorbed proteins can also be fully recovered from the brushes by a simple ionic strength stimulus. The developed systems will find applications as responsive biointerfaces in the fields of separation technologies, biosensing, drug delivery, and nanomedicine.
机译:选择性蛋白质吸附是用于制定生物传感器,分离技术和医学和生物技术的智能材料的关键挑战。在这项工作中,基于使用由聚(环氧乙烷),蛋白质避免的聚合物和聚(丙烯酸)(PAA)组成的混合聚合物刷的使用混合聚合物刷来开发一种策略,用于使用由聚(环氧乙烷)(PEO),蛋白质疏扰聚合物和聚(丙烯酸)(PAA),弱多酸其构象根据周围介质的pH和离子强度而变化。使用溶菌酶(LyZ),人血清白蛋白(HSA)和人纤维蛋白原(FB)的混合物来证明该策略的成功。通过石英晶体微稳定监测聚合物刷形成和蛋白质吸附,而通过飞行时间二次离子质谱(TOF-SIMS)与本金成分分析和银染色,蛋白质鉴定从混合物吸附后。对于TOF-SIMS测量,首先从单蛋白质溶液进行吸附,以识别每种蛋白质的特征峰。接下来,从三种蛋白质的混合物中进行吸附。蛋白质也从刷子中解吸并通过凝胶电泳分析,与银染色以进一步鉴定。从Lyz / HSA / Fb的混合物中选择性吸附Lyz,在pH 9.0和10(3)m的离子强度,而Lyz和HSA,但不是Fb,在离子强度下吸附10(-2)m和ph 9.0。结果表明,通过控制离子强度,可以从PEO / PAA混合刷上的蛋白质混合物中获得选择性吸附,主要是因为所得到的静电相互作用对照。在良好的条件下,选择性吸附的蛋白质也可以通过简单的离子强度刺激从刷子完全回收。发达的系统将在分离技术,生物传感,药物递送和纳米医用的响应性生物界面中找到应用。

著录项

  • 来源
    《Nature reviews neuroscience》 |2019年第2期|共12页
  • 作者单位

    Catholic Univ Louvain Inst Condensed Matter &

    Nanosci Pl Louis Pasteur L4-01-10 B-1348 Louvain;

    Catholic Univ Louvain Inst Condensed Matter &

    Nanosci Pl Louis Pasteur L4-01-10 B-1348 Louvain;

    Catholic Univ Louvain Louvain Inst Biomol Sci &

    Technol Croix Sud 4-S L7-07-14 B-1348 Louvain La;

    Catholic Univ Louvain Louvain Inst Biomol Sci &

    Technol Croix Sud 4-S L7-07-14 B-1348 Louvain La;

    Catholic Univ Louvain Louvain Inst Biomol Sci &

    Technol Croix Sud 4-S L7-07-14 B-1348 Louvain La;

    Catholic Univ Louvain Inst Condensed Matter &

    Nanosci Pl Louis Pasteur L4-01-10 B-1348 Louvain;

    Catholic Univ Louvain Inst Condensed Matter &

    Nanosci Pl Louis Pasteur L4-01-10 B-1348 Louvain;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经生理学;
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