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Postnatal expression pattern of calcium-binding proteins in organotypic thalamic cultures and in the dorsal thalamus in vivo
Authors:F Sieg  K Obst  T Gorba  B Riederer  HC Pape  P Wahle
Affiliation:Fachbereich Chemie, Universit?t Kaiserslautern, D-67653 Kaiserslautern, Germany.
Abstract:We have investigated the influence of the chemical structure and charge of the hydrophillic headgroup on the miscibility of saturated phospholipids with acyl chain lengths differing by two methylene units, namely DMPA/DPPA, DMPC/DPPC, DMPE/DPPE and DMPG/DPPG (0.1 M NaCl). All four mixtures were analysed by DSC at pH 7. To study the influence of a change in headgroup charge, we additionally investigated DMPA/DPPA mixtures at pH 4 and 12, and DMPG/DPPG mixtures at pH 2. The experimental DSC thermograms were fitted using methods described before [Johann et al., Biophys. J. 71 (1996), 3215-3228] to obtain the temperatures of onset and end of melting and first approximations for the non-ideality parameters as a function of composition. The resulting phase diagrams were then fitted using a four non-ideality parameter model for non-ideal, non-symmetric mixing in both phases. The phase diagram of the system DMPG/DPPG has a lens-like shape, the non-ideality parameters rhog and rhol for the gel and the liquid-crystalline phase, respectively, are zero, indicating ideal mixing in both phases. For the other mixtures, differences in miscibility are observed depending on the structure of the headgroup. At pH 7, rhog > rhol, i.e., the miscibility in the liquid-crystalline phase is more ideal than in the gel state. All rhog values are positive and the sequence for rhog observed is PA>PE>PC>PG. Partial protonation of PA at pH 4 or complete deprotonation at pH 12 leads to negative non-ideality parameters for both phases, indicating a preference for mixed pair formation. Protonation of PG in DMPG/DPPG mixtures at pH 2 leads to positive non-ideality parameters for both phases, indicating a tendency for demixing. The results show, that the miscibility of phospholipids with identical headgroups but chain lengths differing by two methylene groups is dependent on headgroup structure and on headgroup charge.
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