Specific ion effects: why the properties of lysozyme in salt solutions follow a Hofmeister series.

Abstract:

:Protein solubility in aqueous solutions depends in a complicated and not well understood way on pH, salt type, and salt concentration. Why for instance does the use of two different monovalent salts, potassium thiocyanate and potassium chloride, produce such different results? One important and previously neglected source of ion specificity is the ionic dispersion potential that acts between each ion and the protein. This attractive potential is found to be much stronger for SCN(-) than it is for Cl(-). We present model calculations, performed within a modified ion-specific double-layer theory, that demonstrate the large effect of including these ionic dispersion potentials. The results are consistent with experiments performed on hen egg-white lysozymes and on neutral black lipid membranes. The calculated surface pH and net lysozyme charge depend strongly on the choice of anion. We demonstrate that the lysozyme net charge is larger, and the corresponding Debye length shorter, in a thiocyanate salt solution than in a chloride salt solution. Recent experiments have suggested that pK(a) values of histidines depend on salt concentration and on ionic species. We finally demonstrate that once ionic dispersion potentials are included in the theory these results can quantitatively be reinterpreted in terms of a highly specific surface pH (and a salt-independent pK(a)).

journal_name

Biophys J

journal_title

Biophysical journal

authors

Boström M,Williams DR,Ninham BW

doi

10.1016/S0006-3495(03)74512-3

subject

Has Abstract

pub_date

2003-08-01 00:00:00

pages

686-94

issue

2

eissn

0006-3495

issn

1542-0086

pii

S0006-3495(03)74512-3

journal_volume

85

pub_type

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