F. Lopezgarcia et al., INTERACTION OF SPHINGOSINE AND STEARYLAMNINE WITH PHOSPHATIDYLSERINE AS STUDIED BY DSC AND NMR, Biochimica et biophysica acta, 1153(1), 1993, pp. 1-8
The interaction of sphingosine (SP) and stearylamine (SA) with dipalmi
toylphosphatidylserine (DPPS) has been studied by using differential s
canning calorimetry (DSC) and phosphorus nuclear magnetic resonance (P
-31-NMR). DSC showed that SP and SA rigidified the membranes, forming
an azeotropic mixture with DPPS. The azeotropic mixture which was form
ed between DPPS and SP was found at a DPPS/SP molar ratio of 2:1 where
as SA and DPPS formed an azeotropic mixture at a DPPS/SA molar ratio o
f 1:1. An eutectic point was observed at 85 mol% of SP and 90 mol% of
SA in DPPS. P-31-NMR showed the presence of a lamellar phase at DPPS/S
P and DPPS/SA molar ratios lower than 1:1, whereas at higher molar rat
ios and at high temperatures, besides the lamellar phase, an isotropic
component was detected. It was found that, at physiological pH, both
SP and SA were protonated in a large extent, i.e., positively charged,
since their apparent pK in the membrane were 9.1 and 8.9, respectivel
y. The results reported in this work may be relevant to understand a n
umber of biological effects produced by these positively charged molec
ules, due to their electrostatic interaction with negatively charged p
hospholipids.