Why pH titration in lysozyme suspensions follow a Hofmeister series

被引:10
|
作者
Bostrom, M. [1 ]
Ninham, B. W.
机构
[1] Linkoping Univ, Dept Phys Chem & Biol, SE-58183 Linkoping, Sweden
[2] Univ Florence, Dept Chem & CSGI, I-50019 Florence, Italy
[3] Australian Natl Univ, Res Sch Phys Sci & Engn, Canberra, ACT 0200, Australia
关键词
Hofmeister effect; polarizability; ionic dispersion potentials; lysozyme; Poisson-Boltzmann equation;
D O I
10.1016/j.colsurfa.2006.06.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present theoretical results that provide new insights into the Hofmeister effects observed in protein suspensions. With a buffered solution at a supposedly fixed pH, measurements of that pH with glass electrodes in protein suspensions depend strongly on both ionic species and concentration of background salt and protein. The observed Hofmeister series cannot be explained with standard electrostatic theories. While purely electrostatic limiting laws can be used to obtain partial understanding of some nonspecific trends in buffer and protein solutions, it has long been clear that they fail to explain such ion specificity. The reasons, as explored in a number of our previous papers, have to do with the neglect in these theories of electrodynamic fluctuation (dispersion) forces between ions and proteins. We here use a Poisson-Boltzmann cell model that takes these ionic dispersion potentials between ions and protein into account. The observed ion specificity can then be accounted for. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:24 / 29
页数:6
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