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Bicellar model membranes composed of 1,2-dimyristoylphosphatidylcholine (DMPC) and 1,2-dihexanoylphosphatidylcholine (DHPC), with a DMPC/DHPC molar ratio of 5, and doped with the negatively charged lipid 1,2-dimyristoylphosphatidylglycerol (DMPG), at DMPG/DMPC molar ratios of 0.02 or 0.1, were examined using small angle neutron scattering (SANS), 31 P NMR, and 1 H pulsed field gradient (PFG) diffusion NMR with the goal of understanding temperature effects on the DHPC-dependent perforations in these self-assembled membrane mimetics. Over the temperature range studied via SANS (300À330 K), these bicellar lipid mixtures exhibited a well-ordered lamellar phase. The interlamellar spacing d increased with increasing temperature, in direct contrast to the decrease in d observed upon increasing temperature with otherwise identical lipid mixtures lacking DHPC. 31 P NMR measurements on magnetically aligned bicellar mixtures of identical composition indicated a progressive migration of DHPC from regions of high curvature into planar regions with increasing temperature, and in accord with the "mixed bicelle model" (Triba, M. N.; Warschawski, D. E.; Devaux, P. E. Biophys. J. 2005, 88, 1887À1901). Parallel PFG diffusion NMR measurements of transbilayer water diffusion, where the observed diffusion is dependent on the fractional surface area of lamellar perforations, showed that transbilayer water diffusion decreased with increasing temperature. A model is proposed consistent with the SANS, 31 P NMR, and PFG diffusion NMR data, wherein increasing temperature drives the progressive migration of DHPC out of highcurvature regions, consequently decreasing the fractional volume of lamellar perforations, so that water occupying these perforations redistributes into the interlamellar volume, thereby increasing the interlamellar spacing.

Diffusion coefficients of hydrophobically modified alkali-swellable (HASE) associating polymers (APs) in aqueous solution were measured using pulsed gradient spin-echo (PGSE) nuclear magnetic resonance (NMR). HASE APs consist of a copolymer of methacrylic acid and ethyl acrylate to which hydrophobic “sticker groups” are attached through a poly(ethylene oxide) (PEO) “spacer arm”. Two series of HASE APs were investigated:  one in which the length of the hydrophobic alkyl chain was varied (C x E35) and another in which the length of the PEO spacer arm was varied (C20E y ). With increasing hydrophobe or PEO spacer arm length the average diffusion coefficient decreased, reflecting the viscosity enhancement produced by the associating network formed by HASE polymers. The effect of external variables such as concentration, pH, and temperature mirrored established rheological properties for such systems. The average diffusion behavior, however, was the result of a superposition of two contributions, one slow (D 0 < 1 × 10-11 m2 s-1) and one fast (D 0 ≈ 1 × 10-10 m2 s-1) diffusing. Changing the hydrophobe chain length or the PEO spacer arm length modulated the proportion of the fast and slow diffusing populations but had relatively little effect on the diffusion coefficients of the two populations. Precipitation of the HASE AP from THF−HClaq produced two fractions, one enriched with hydrophobe and the other correspondingly depleted relative to the global average. The fractions enriched and depleted with respect to hydrophobe exhibited diffusion coefficients similar to the fast and slow diffusing populations. We conclude that the hydrophobe is inhomogeneously distributed among the HASE AP chains, that the population enriched with hydrophobe forms more compact structures capable of faster diffusion, and that the effects of hydrophobe chain length and PEO spacer arm length on HASE AP solution viscosity are mediated by their influence on the coupling of the hydrophobe enriched population into the slow-diffusing hydrophobe-depleted population.

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