Probing The Formation And Conformational Relaxation Of Previtamin D-3 And Analogues In Solution And In Lipid Bilayers

The photosynthesis of vitamin D-3 in mammalian skin results from UV-B irradiation of provitamin D-3 (7-dehydro-cholesterol, DHC) at ca. 290 nm. Upon return to the ground state, the hexatriene product, previtamin D-3, undergoes a conformational equilibration between helical gZg and more planar tZg and tZt forms. The helical gZg forms provide a pathway for the formation of vitamin D 3 via a [1,7]-sigmatropic hydrogen shift. Steady state photolysis and UV transient absorption spectroscopy are combined to explore the conformational relaxation of previtamin D-3 formed from DHC in isotropic solution and confined to lipid bilayers chosen to model the biological cell membrane. The results are compared with measurements for two analogues: previtamin D-2 formed from ergosterol (provitamin D-2) and previtamin D-3 acetate formed from DHC acetate. The resulting spectral dynamics are interpreted in the context of simulations of optical excitation energy and oscillator strength as a function of conformation. In solution, the relaxation dynamics and steady state product distributions of the three compounds are nearly identical, favoring tZg forms. When confined to lipid bilayers, the heterogeneity and packing forces alter the conformational distributions and enhance the population of a gZg conformer capable of vitamin D formation.