Life requires a delicate balance between cell membrane rigidity and fluidity to define cell boundaries yet enable cell deformation, growth, and division. Here, we bridge the molecular and macroscopic scales with neutron scattering techniques to demonstrate how the material properties of model lipid membranes are readily tuned by the constituent lipid composition. Mixing lipids leads to softer and less viscous membranes than predicted a priori from the pure component membrane properties. Instead, the dynamics are linked to the membrane structure and follow simple scaling relationships with the area per molecule. These results emphasize the importance of lipid packing and reveal the interwoven relationship between lipid membrane structure and dynamics.
The elastic and viscous properties of biological membranes play a vital role in controlling cell functions that require local reorganization of the membrane components as well as dramatic shape changes such as endocytosis, vesicular trafficking, and cell division. These properties are widely acknowledged to depend on the unique composition of lipids within the membrane, yet the effects of lipid mixing on the membrane biophysical properties remain poorly understood. Here, we present a comprehensive characterization of the structural, elastic, and viscous properties of fluid membranes composed of binary mixtures of lipids with different tail lengths. We show that the mixed lipid membrane properties are not simply additive quantities of the single-component analogs. Instead, the mixed membranes are more dynamic than either of their constituents, quantified as a decrease in their bending modulus, area compressibility modulus, and viscosity. While the enhanced dynamics are seemingly unexpected, we show that the measured moduli and viscosity for both the mixed and single-component bilayers all scale with the area per lipid and collapse onto respective master curves. This scaling links the increase in dynamics to mixing-induced changes in the lipid packing and membrane structure. More importantly, the results show that the membrane properties can be manipulated through lipid composition the same way bimodal blends of surfactants, liquid crystals, and polymers are used to engineer the mechanical properties of soft materials, with broad implications for understanding how lipid diversity relates to biomembrane function.