Electrophoretic mobilities of neutral analytes and electroosmotic flow markers in aqueous solutions of Hofmeister salts
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24338984
DOI
10.1002/elps.201300544
Knihovny.cz E-zdroje
- Klíčová slova
- EOF markers, Ion-specific effects, Ion-specific mobilization, Molecular dynamics simulations, Neutral analytes,
- MeSH
- acetamidy chemie MeSH
- cesium chemie MeSH
- dimethylsulfoxid chemie MeSH
- elektroforéza kapilární metody MeSH
- elektroosmóza MeSH
- lithium chemie MeSH
- osmolární koncentrace MeSH
- roztoky MeSH
- simulace molekulární dynamiky MeSH
- soli MeSH
- thiomočovina chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetamidy MeSH
- cesium MeSH
- dimethylsulfoxid MeSH
- lithium MeSH
- N-methylacetamide MeSH Prohlížeč
- roztoky MeSH
- soli MeSH
- thiomočovina MeSH
Small neutral organic compounds have traditionally the role of EOF markers in electrophoresis, as they are expected to have zero electrophoretic mobility in external electric fields. The BGE contains, however, ions that have unequal affinities to the neutral molecules, which in turn results in their mobilization. In this study we focused on two EOF markers-thiourea and DMSO, as well as on N-methyl acetamide (NMA) as a model of the peptide bond. By means of CE and all atom molecular dynamics simulations we explored mobilization of these neutral compounds in large set of Hofmeister salts. Employing a statistical mechanics approach, we were able to reproduce by simulations the experimental electrophoretic mobility coefficients. We also established the role of the chemical composition of marker and the BGE on the measured electrophoretic mobility coefficient. For NMA, we interpreted the results in terms of the relative affinities of cations versus anions to the peptide bond.
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