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溶菌酶在阳离子交换剂上的吸附:基于保留色谱数据分析的相互作用机制研究

Lysozyme adsorption onto a cation-exchanger: mechanism of interaction study based on the analysis of retention chromatographic data.

作者信息

Marques F S, Silva G L, Thrash M E, Dias-Cabral A C

机构信息

CICS-UBI - Health Sciences Research Centre, University of Beira Interior, 6200-506 Covilhã, Portugal; Department of Chemistry, University of Beira Interior, 6201-001 Covilhã, Portugal.

Department of Water Resources Management and Environmental Engineering, College of Science and Engineering, Central State University, Wilberforce, OH, USA.

出版信息

Colloids Surf B Biointerfaces. 2014 Oct 1;122:801-807. doi: 10.1016/j.colsurfb.2014.08.024. Epub 2014 Aug 26.

Abstract

In this study, based on the analysis of retention chromatographic data, we examined the adsorption of lysozyme onto carboxymethyl cellulose. Lysozyme retention data was collected at pH 5 and pH 8. The sodium chloride (NaCl) concentration in the mobile phase ranged from 300mM to 500mM and the temperature for this study varied from 288K to 308K. The retention measurements generated from these experimental conditions were analyzed with the Van't Hoff method, the preferential interaction model and the stoichiometric displacement model. Endothermic heats-of-adsorption and increases in entropy were observed under certain experimental conditions. These data suggest the presence of entropic driving forces such as the release of water and/or possibly structural changes in lysozyme molecules adsorbed to the surface of carboxymethyl cellulose. The modest observed exergonic adsorption ΔG° and the preferential interaction analysis corroborate the presence of water-release for this study. Additional analysis with the stoichiometric displacement model method revealed negligible changes in the structure of lysozyme molecules in contact with the surface of carboxymethyl cellulose.

摘要

在本研究中,基于保留色谱数据的分析,我们研究了溶菌酶在羧甲基纤维素上的吸附情况。在pH 5和pH 8条件下收集了溶菌酶保留数据。流动相中氯化钠(NaCl)浓度范围为300mM至500mM,本研究的温度范围为288K至308K。利用范特霍夫方法、优先相互作用模型和化学计量置换模型对这些实验条件下产生的保留测量值进行了分析。在某些实验条件下观察到了吸热吸附热和熵增加。这些数据表明存在熵驱动力,如吸附在羧甲基纤维素表面的溶菌酶分子释放水和/或可能发生的结构变化。观察到的适度放能吸附ΔG°和优先相互作用分析证实了本研究中存在水释放现象。用化学计量置换模型方法进行的额外分析表明,与羧甲基纤维素表面接触的溶菌酶分子结构变化可忽略不计。

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