Cantù L, Corti M, Del Favero E, Digirolamo E, Sonnino S, Tettamanti G
Department of Medical Chemistry and Biochemistry, Medical School, University of Milan, Italy.
Chem Phys Lipids. 1996 Mar 29;79(2):137-45. doi: 10.1016/0009-3084(96)02521-2.
The present paper reports the experimental observation of an interesting thermodynamic process which could be biologically important: such behaviour, shown by some gangliosides, is likely to be peculiar of these glycosidic compounds as it has never been observed for other membrane-type amphiphilic molecules. In water solution, gangliosides have been found to present a bistable behaviour between two stable states (called A and B) which does not involve any change in the primary structure of the molecule. The interconversion between state A and state B, and vice versa, does not occur spontaneously, but has to be triggered by some external agent, which makes this system a potentially regulated process with important biological correlations. In the present experiments, state B is reached from state A with a temperature rise in the range 30-55 degrees C. The new state is stable regardless of any possible temperature cycle. The initial state A is then regained when the ganglioside solution is dried and the solute is redissolved. The two states are believed to correspond to two different conformations of the hydrophilic portion of the molecule. The bistable behaviour is shown by the gangliosides GM2, GM1, GD1a, GD1b and Fuc-GD1b, GT1b, however, does not show such an effect.
