📝 SummarXiv

Abstract

During the melting transition of dimyristoyl phosphatidylglycerol (DMPG), the order of the lipid chains and the three-dimensional, vesicular structural arrangement change simultaneously. These changes result in peculiar heat capacity profiles extended over a broad temperature range with seven $c_p$-maxima. Here, we present calorimetric, viscosity, and volume expansion coefficient data at various ionic strengths and charges. We propose a simple theory that explains the calorimetric data in terms of the coexistence of two membrane geometries, both of which can melt. During the transition, the equilibrium between these two geometries changes cooperatively. This equilibrium depends on the interactions between the membranes and the solvent, on the membrane's charge and the ionic strength of the buffer. Solvent interactions also contribute to the volume change of the membrane phases. Unlike uncharged membranes, we find that enthalpy changes are no longer proportional to volume changes. Therefore, the pressure dependence of the calorimetric profiles differs from that of uncharged membranes. Our theory explains the pressure dependence of calorimetric profiles qualitatively and quantitatively. Furthermore, we demonstrate that the same theory can be used to describe pretransition and ripple formation in phosphatidylcholines. A key takeaway from this article is that solvent molecules (e.g., H2O) are part of the membrane and, in the case of DMPG, water cannot be considered a separate phase.