Interactions of La³⁺ with phosphatidylserine vesicles Binding, phase transition, leakage, ³¹P-NMR and fusion

The interaction of La³⁺ with phosphatidylserine vesicles is studied by differential scanning calorimetry, ¹⁴⁰La binding, ³¹P-NMR chemical shifts and relaxation rates, carboxyfluorescein and [¹⁴C]sucrose release, X-ray diffraction and freeze-fracture electron microscopy. In the presence of La³⁺ concentrations above 1 mM and an incubation temperature of 38°C, i.e., at the phase transition temperature of the complex La/phosphatidylserine, the binding ratio of La/lipid exceeds a 1 3 ratio, reaching saturation at a 1 2 ratio. Analysis, employing a modified Gouy-Chapman equation, indicates a significant increase in the intrinsic binding constant of La/phosphatidylserine when the La³⁺ concentration exceeds the threshold concentration for leakage. The analysis illustrates that at the molecular level the binding of La³⁺ can be comparable to or even weaker than that of Ca²⁺, but that even when present at smaller concentrations La³⁺ competes with and partially displaces Ca²⁺ from membranes or other negatively charged surfaces. The results suggest that the sequence La³⁺>Ca²⁺>Mg²⁺ reflects both the binding strength of these cations to phosphatidylserine as well as their ability to induce leakage, enhancement of ³¹P spin-lattice relaxation rates, fusion and other structural changes. The leakage, fusion, and other structural changes are more pronounced at the phase transition temperature of the La/lipid complex.