AbstractThe Hofmeister effect consists in changes of protein solubility triggered by neutral electrolyte cosolutes. Based on the assumption that salts cause stochastic fluctuations of the free energy barrier profiles, a kinetic theory of this phenomenon is proposed. An exponentially correlated noise, of amplitude proportional to the salt concentration, is added to each energy level, and the time-dependence of the mean protein concentration is calculated. It is found that the theory yields the well-known Setschenow equation if the noise correlation time is low in comparison to the aggregation time constant. Experimental data on salting-in agents are well fitted, whereas, in the case of salting-out cosolutes, two independent dichotomic fluctu...
ABSTRACT Model compound studies in the literature show how Hofmeister ion interactions affect protei...
Protein interactions in solution are conveniently analysed with small angle X-ray scattering (SAXS)....
We performed molecular dynamics simulations on the tryptophane-cage miniprotein using a nonpolarizab...
In order to understand the origin of the Hofmeister series, a statistical-mechanical analysis, based...
Protein solubility, protein charge and acid-base titration in protein solutions depend strongly on t...
We present theoretical results that provide new insights into the Hofmeister effects observed in pro...
Protein solubility studies below the isoelectric point exhibit a direct Hofmeister series at high sa...
Protein solubility studies below the isoelectric point exhibit a direct Hofmeister series at high sa...
Measurements of pH in single-phase cytochrome c suspensions are reported. The pH, as determined by a...
Specific effects of electrolytes have posed a challenge since the 1880's. The pioneering work was th...
Model compound studies in the literature show how Hofmeister ion interactions affect protein stabili...
<div><p>Hofmeister effects have been recognized as important as Mendel’s work was to genetics while ...
The salting-out effect of simple electrolytes on lysozyme has been studied by measuring the second v...
Protein aggregation via liquid–liquid phase separation (LLPS) is ubiquitous in nature and is intimat...
AbstractUnderstanding the screening by salts of charge-charge interactions in proteins is important ...
ABSTRACT Model compound studies in the literature show how Hofmeister ion interactions affect protei...
Protein interactions in solution are conveniently analysed with small angle X-ray scattering (SAXS)....
We performed molecular dynamics simulations on the tryptophane-cage miniprotein using a nonpolarizab...
In order to understand the origin of the Hofmeister series, a statistical-mechanical analysis, based...
Protein solubility, protein charge and acid-base titration in protein solutions depend strongly on t...
We present theoretical results that provide new insights into the Hofmeister effects observed in pro...
Protein solubility studies below the isoelectric point exhibit a direct Hofmeister series at high sa...
Protein solubility studies below the isoelectric point exhibit a direct Hofmeister series at high sa...
Measurements of pH in single-phase cytochrome c suspensions are reported. The pH, as determined by a...
Specific effects of electrolytes have posed a challenge since the 1880's. The pioneering work was th...
Model compound studies in the literature show how Hofmeister ion interactions affect protein stabili...
<div><p>Hofmeister effects have been recognized as important as Mendel’s work was to genetics while ...
The salting-out effect of simple electrolytes on lysozyme has been studied by measuring the second v...
Protein aggregation via liquid–liquid phase separation (LLPS) is ubiquitous in nature and is intimat...
AbstractUnderstanding the screening by salts of charge-charge interactions in proteins is important ...
ABSTRACT Model compound studies in the literature show how Hofmeister ion interactions affect protei...
Protein interactions in solution are conveniently analysed with small angle X-ray scattering (SAXS)....
We performed molecular dynamics simulations on the tryptophane-cage miniprotein using a nonpolarizab...