Electrophoretic mobilities of neutral analytes and electroosmotic flow markers in aqueous solutions of Hofmeister salts
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- Keywords
- EOF markers, Ion-specific effects, Ion-specific mobilization, Molecular dynamics simulations, Neutral analytes,
- MeSH
- Acetamides chemistry MeSH
- Cesium chemistry MeSH
- Dimethyl Sulfoxide chemistry MeSH
- Electrophoresis, Capillary methods MeSH
- Electroosmosis MeSH
- Lithium chemistry MeSH
- Osmolar Concentration MeSH
- Solutions MeSH
- Molecular Dynamics Simulation MeSH
- Salts MeSH
- Thiourea chemistry MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acetamides MeSH
- Cesium MeSH
- Dimethyl Sulfoxide MeSH
- Lithium MeSH
- N-methylacetamide MeSH Browser
- Solutions MeSH
- Salts MeSH
- Thiourea 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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