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H Träuble

Publications and source records attributed to H Träuble.

14 recordsLinked to original sources

Mechanistic interpretation of the influence of lipid phase transitions on transport functions.

In an attempt to understand the mechanism by which a structural change of membrane lipids affects transport functions, the temperature dependence of transport rate has been measured to below the low temperature end of the fluid in equilibrium ordered phase transition of the membrane lipids. The unsaturated fatty acid requiring Escherichia coli strain T105 was supplemented with either trans-delta9-octadecenoate or trans-delta9-hexadecenoate or supplemented with and subsequently starved for cis-delta9-octadecenoate. Fluid in equilibrium ordered phase transitions measured in whole cells using the fluorescence probe N-phenyl-1-naphthylamine were compared with the temperature dependence of beta-glucoside and beta-galactoside transport. In addition to the previously observed downward "break" in the Arrhenius plot of transport rate which occurred near the middle of the phase transition temperature range, a second upward "break" was observed which could be correlated with the low-temperature end of the phase transition. These experiments are interpreted in terms of a partitioning of transport proteins between ordered and fluid domains which is described by a lateral distribution coefficient, k. This distribution coefficient varies with the membrane lipid composition as well as with the transport system. Values for k suggest a 2-20-fold preference for the partitioning of transport proteins into the fluid parts of the membrane.

Biological Transport

Electrostatic effects on lipid phase transitions: membrane structure and ionic environment.

Ordered --> fluid phase transitions in bilayers of charged lipids are accompanied by a decrease in electrostatic free energy mainly as a result of bilayer expansion. For uniform charge distribution the Gouy-Chapman theory of the electrical double layer predicts a decrease of the transition temperature with increasing charge density. We studied the effects of pH and mono- and divalent cations on the phase transition of lecithin, cephalin, phosphatidylserine, and phosphatidic acid bilayers. Phosphatidic acid with two ionizable protons was selected for a systematic investigation. A change in pH from 7 to 9 increases the charge per polar group from one to two elementary charges. This lowers the transition temperature by about 20 degrees C in agreement with the theory. In this pH region rather small changes in pH suffice to induce the phase transition at constant temperature. Divalent cations (Mg(++) and Ca(++)) increase the transition temperature by charge neutralization and thus can be used to induce the fluid --> ordered transition at constant temperature. In contrast, monovalent cations (Li(+), Na(+), K(+)) lower the transition temperature, or fluidize the bilayer structure at a given temperature. Rather small changes in ionic environment can induce gross alterations in bilayer structure; divalent and monovalent cations have antagonistic effects. This result parallels current theories on nerve excitation and sensory transduction where cation-induced structural changes in biomembranes are invoked.

Calcium