Aggregational behavior of aqueous dispersions of the antifungal lipopeptide iturin A

• Published in: Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2001, Vol.22 (1), p.1-5
• Main Authors: Grau, Alicia, Gómez-Fernández, Juan C., Peypoux, Françoise, Ortiz, Antonio
• Format: Article
• Language: English
• Subjects: Anti-Bacterial Agents - chemistry; Anti-Bacterial Agents - pharmacology; Antifungal Agents - chemistry; Antifungal Agents - pharmacology; Bacillus subtilis; Interdigitated bilayers; Iturin; Lipopeptides; Peptides; Peptides, Cyclic; Protein Binding
• ISSN: 0196-9781; 1873-5169
• DOI: 10.1016/S0196-9781(00)00350-8

Iturin A, a lipopeptide isolated from Bacillus subtilis, posses a strong antifungal activity, and has been devoted to a great deal of attention. Since iturin is an amphiphilic compound with a great propensity to self-associate in solution as well as inside the membrane, the question arises to whether its aggregational behavior is dependent on the concentration of the lipopeptide. In order to test this, the ability of iturin suspensions to encapsulate water-soluble molecules has been examined. Iturin was dispersed at different concentrations above its critical micellar concentration, in a buffer containing the water-soluble dye 5,6-carboxyfluorescein. For iturin A micelles, a Stokes radius of 1.3 nm and an aggregational number of 7 was obtained. The results shown in this work clearly demonstrate that iturin dispersions in water, at concentrations of 0.7, 1.4 and 3 mM, i.e. far above the critical micellar concentration (40 μM), are capable of encapsulating carboxyfluorescein, probably by adopting a type of aggregate different from the micelle. Negative-staining electron microscopy shows the presence of vesicles with an average size of 150 nm. By using 14C-iturin, it is shown that, at 3 mM concentration, 40% of the iturin molecules adopt this vesicular state. It is proposed that iturin molecules form a fully interdigitated bilayer, where each hydrocarbon tail span the entire hydrocarbon width of the bilayer, resulting in multilamellar vesicles capable of encapsulating an aqueous compartment. The possible implications of these results to the membrane destabilizing effect of iturin A, are discussed according to the dynamic cone-shape of the iturin molecule.