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带相反电荷纳米颗粒混合物的相行为:应用于溶菌酶和琥珀酰化溶菌酶的非均匀泊松-玻尔兹曼池模型

Phase behavior of mixtures of oppositely charged nanoparticles: heterogeneous Poisson-Boltzmann cell model applied to lysozyme and succinylated lysozyme.

作者信息

Biesheuvel P Maarten, Lindhoud Saskia, de Vries Renko, Cohen Stuart Martien A

机构信息

Laboratory of Physical Chemistry and Colloid Science, Wageningen University, Dreijenplein 6, 6703 HB Wageningen, The Netherlands.

出版信息

Langmuir. 2006 Jan 31;22(3):1291-300. doi: 10.1021/la052334d.

Abstract

We study the phase behavior of mixtures of oppositely charged nanoparticles, both theoretically and experimentally. As an experimental model system we consider mixtures of lysozyme and lysozyme that has been chemically modified in such a way that its charge is nearly equal in magnitude but opposite in sign to that of unmodified lysozyme. We observe reversible macroscopic phase separation that is sensitive not only to protein concentration and ionic strength, but also to temperature. We introduce a heterogeneous Poisson-Boltzmann cell model that generally applies to mixtures of oppositely charged nanoparticles. To account for the phase behavior of our experimental model system, in addition to steric and electrostatic interactions, we need to include a temperature-dependent short-ranged interaction between the lysozyme molecules, the exact origin of which is unknown. The strength and temperature dependence of the short-ranged attraction is found to be of the same order of magnitude as that between unmodified lysozyme molecules. The presence of a rather strong short-ranged attraction in our model system precludes the formation of colloidal liquid phases (or complex coacervates) such as those typically found in mixtures of globular protein molecules and oppositely charged polyelectrolytes.

摘要

我们从理论和实验两方面研究了带相反电荷的纳米颗粒混合物的相行为。作为一个实验模型系统,我们考虑了溶菌酶与经过化学修饰的溶菌酶的混合物,其修饰方式使得修饰后的溶菌酶电荷大小与未修饰的溶菌酶几乎相等,但符号相反。我们观察到了可逆的宏观相分离,这种相分离不仅对蛋白质浓度和离子强度敏感,对温度也敏感。我们引入了一种异质泊松 - 玻尔兹曼细胞模型,该模型普遍适用于带相反电荷的纳米颗粒混合物。为了解释我们实验模型系统的相行为,除了空间位阻和静电相互作用外,我们还需要考虑溶菌酶分子之间一种与温度有关的短程相互作用,其确切来源尚不清楚。发现这种短程吸引力的强度和温度依赖性与未修饰的溶菌酶分子之间的短程吸引力处于同一数量级。我们模型系统中存在相当强的短程吸引力,这排除了胶体液相(或复合凝聚层)的形成,而在球状蛋白质分子与带相反电荷的聚电解质的混合物中通常会出现这种胶体液相。

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