Calcium Triggered Lα-H2 Phase Transition Monitored by Combined Rapid Mixing and Time-Resolved Synchrotron SAXSReportar como inadecuado




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Background

Awad et al. 1 reported on the Ca2+-induced transitions of dioleoyl-phosphatidylglycerol DOPG-monoolein MO vesicles to bicontinuous cubic phases at equilibrium conditions. In the present study, the combination of rapid mixing and time-resolved synchrotron small-angle X-ray scattering SAXS was applied for the in-situ investigations of fast structural transitions of diluted DOPG-MO vesicles into well-ordered nanostructures by the addition of low concentrated Ca2+ solutions.

Methodology-Principal Findings

Under static conditions and the in absence of the divalent cations, the DOPG-MO system forms large vesicles composed of weakly correlated bilayers with a d-spacing of ∼140 Å Lα-phase. The utilization of a stopped-flow apparatus allowed mixing these DOPG-MO vesicles with a solution of Ca2+ ions within 10 milliseconds ms. In such a way the dynamics of negatively charged PG to divalent cation interactions, and the kinetics of the induced structural transitions were studied. Ca2+ ions have a very strong impact on the lipidic nanostructures. Intriguingly, already at low salt concentrations DOPG-Ca2+>2, Ca2+ ions trigger the transformation from bilayers to monolayer nanotubes inverted hexagonal phase, H2. Our results reveal that a binding ratio of 1 Ca2+ per 8 DOPG is sufficient for the formation of the H2 phase. At 50°C a direct transition from the vesicles to the H2 phase was observed, whereas at ambient temperature 20°C a short lived intermediate phase possibly the cubic Pn3m phase coexisting with the H2 phase was detected.

Conclusions-Significance

The strong binding of the divalent cations to the negatively charged DOPG molecules enhances the negative spontaneous curvature of the monolayers and causes a rapid collapsing of the vesicles. The rapid loss of the bilayer stability and the reorganization of the lipid molecules within ms support the argument that the transition mechanism is based on a leaky fusion of the vesicles.



Autor: Anan Yaghmur , Peter Laggner, Barbara Sartori, Michael Rappolt

Fuente: http://plos.srce.hr/



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