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{壳聚糖/透明质酸}n层层组装膜对肌红蛋白的负载行为:一项电化学研究。

Loading behavior of {chitosan/hyaluronic acid}n layer-by-layer assembly films toward myoglobin: an electrochemical study.

作者信息

Lu Haiyun, Hu Naifei

机构信息

Department of Chemistry, Beijing Normal University, Beijing 100875, China.

出版信息

J Phys Chem B. 2006 Nov 30;110(47):23710-8. doi: 10.1021/jp063550d.

DOI:10.1021/jp063550d
PMID:17125331
Abstract

When {CS/HA}n layer-by-layer films assembled by oppositely charged chitosan (CS) and hyaluronic acid (HA) were immersed in myoglobin (Mb) solution at pH 5.0, Mb was gradually loaded into the {CS/HA}n films, designated as {CS/HA}n-Mb. The cyclic voltammetric (CV) peak pair of Mb FeIII/FeII redox couple for {CS/HA}n-Mb films on pyrolytic graphite (PG) electrodes was used to investigate the loading behavior of {CS/HA}n films toward Mb. The various influencing factors, such as the number of bilayers (n), the pH of Mb loading solution, and the ionic strength of solution, were investigated by different electrochemical methods and other techniques. The results showed that the main driving force for the bulk loading of Mb was most probably the electrostatic interaction between oppositely charged Mb in solution and HA in the films, while other interactions such as hydrogen bonding and hydrophobic interaction may also play an important role. Other polyelectrolyte multilayer (PEM) films with different components were compared with {CS/HA}n films in permeability and Mb loading, and electroactive probes with different size and surface charge were compared in their incorporation into PEM films. The results suggest that due to the unique structure of CS and HA, {CS/HA}n films with relatively low charge density are packed more loosely and more easily swelled by water, and have better permeability, which may lead to the higher loading amount and shorter loading time for Mb. The protein-loaded PEM films provide a new route to immobilize redox proteins on electrodes and realize the direct electrochemistry of the proteins.

摘要

当由带相反电荷的壳聚糖(CS)和透明质酸(HA)逐层组装而成的{CS/HA}n薄膜在pH 5.0的肌红蛋白(Mb)溶液中浸泡时,Mb会逐渐加载到{CS/HA}n薄膜中,命名为{CS/HA}n-Mb。利用热解石墨(PG)电极上{CS/HA}n-Mb薄膜的Mb FeIII/FeII氧化还原对的循环伏安(CV)峰对来研究{CS/HA}n薄膜对Mb的加载行为。通过不同的电化学方法和其他技术研究了各种影响因素,如双层数(n)、Mb加载溶液的pH值以及溶液的离子强度。结果表明,Mb大量加载的主要驱动力很可能是溶液中带相反电荷的Mb与薄膜中HA之间的静电相互作用,而其他相互作用如氢键和疏水相互作用也可能起重要作用。将具有不同组分的其他聚电解质多层(PEM)薄膜与{CS/HA}n薄膜在渗透性和Mb加载方面进行了比较,并将具有不同尺寸和表面电荷的电活性探针在其掺入PEM薄膜方面进行了比较。结果表明,由于CS和HA的独特结构,电荷密度相对较低的{CS/HA}n薄膜堆积更松散,更易被水膨胀,且具有更好的渗透性,这可能导致Mb的加载量更高且加载时间更短。负载蛋白质的PEM薄膜为将氧化还原蛋白固定在电极上并实现蛋白质的直接电化学提供了一条新途径。

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