KINETICS AND MECHANISM OF THE PRESSURE-INDUCED LAMELLAR ORDER-DISORDER TRANSITION IN PHOSPHATIDYLETHANOLAMINE - A TIME-RESOLVED X-RAY-DIFFRACTION STUDY

By using synchrotron radiation, a movie was made of the X-ray scattering pattern from a biological liquid crystal undergoing a phase transition induced by a pressure jump. The system studied includes the fully hydrated phospholipid dihexadecylphosphatidylethanolamine in the lamellar gel (L-beta') phase at a temperature of 68-degrees-C and a pressure of 9.7 MPa (1400 psig). Following the rapid release of pressure to atmospheric the L-beta' phase transforms slowly into the lamellar liquid crystal (L-alpha) phase. The pressure perturbation is applied with the intention of producing a sudden phase disequilibrium followed by monitoring the system as it relaxes to its new equilibrium condition. Remarkably, the proportion of sample in the L-alpha phase grows linearly with time, taking 37 s to totally consume the L-beta' phase. The time dependencies of radius, peak intensity, and width of the powder diffraction ring of the low-angle (001) lamellar reflections were obtained from the movie by image processing. The concept of an "effective pressure" is introduced to account for the temperature variations that accompany the phase transition and to establish that the observed large transit time is indeed intrinsic to the sample and not due to heat exchange with the environment. The reverse transformation, L-alpha to L-beta', induced by a sudden jump from atmospheric pressure to 9.7 MPa, is complete in less than 13 s. These measurements represent a new approach for studying the kinetics of lipid phase transitions and for gaining insights into the mechanism of the lamellar order/disorder transition.