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Determination of stability constants of valinomycin complexes with ammonium and alkali metal ions by capillary affinity electrophoresis
S Ehala, V Kasicka, E Makrlik
Jazyk angličtina Země Německo
PubMed
18200647
DOI
10.1002/elps.200700583
Knihovny.cz E-zdroje
- MeSH
- alkálie chemie MeSH
- antibakteriální látky chemie MeSH
- elektroforéza kapilární metody MeSH
- financování organizované MeSH
- ionofory chemie MeSH
- kationty jednomocné chemie MeSH
- kvartérní amoniové sloučeniny chemie MeSH
- stabilita léku MeSH
- valinomycin analogy a deriváty chemie MeSH
Capillary affinity electrophoresis (CAE) has been employed to investigate quantitatively the interactions of valinomycin, macrocyclic depsipeptide antibiotic ionophore, with univalent cations, ammonium and alkali metal ions, K(+), Cs(+), Na(+), and Li(+), in methanol. The study involved measuring the change in effective electrophoretic mobility of valinomycin while the cation concentrations in the BGE were increased. The corresponding apparent stability (binding) constants of the valinomycin-univalent cation complexes were obtained from the dependence of valinomycin effective mobility on the cation concentration in BGE using a nonlinear regression analysis. The calculated apparent stability constants of the above-mentioned complexes show the substantially higher selectivity of valinomycin for K(+) and Cs(+) ions over Li(+), Na(+), and NH(4)(+) ions. CAE proved to be a suitable method for the investigation of both weak and strong interactions of valinomycin with small ions.
Citace poskytuje Crossref.org
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- $a Capillary affinity electrophoresis (CAE) has been employed to investigate quantitatively the interactions of valinomycin, macrocyclic depsipeptide antibiotic ionophore, with univalent cations, ammonium and alkali metal ions, K(+), Cs(+), Na(+), and Li(+), in methanol. The study involved measuring the change in effective electrophoretic mobility of valinomycin while the cation concentrations in the BGE were increased. The corresponding apparent stability (binding) constants of the valinomycin-univalent cation complexes were obtained from the dependence of valinomycin effective mobility on the cation concentration in BGE using a nonlinear regression analysis. The calculated apparent stability constants of the above-mentioned complexes show the substantially higher selectivity of valinomycin for K(+) and Cs(+) ions over Li(+), Na(+), and NH(4)(+) ions. CAE proved to be a suitable method for the investigation of both weak and strong interactions of valinomycin with small ions.
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