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    Interaction of isolinderanolide E obtained from Nectandra oppositifolia with biomembrane models

    Year: 2021

    Journal: Biochim. Biophys. Acta-Biomembr., Volume 1863, OCT

    Authors: Rosa, Matheus Elias; Alves Conserva, Geanne A.; Lago, Joao Henrique G.; Caseli, Luciano

    Organizations: FAPESP [2019/03239-0, 2018/22214-6, 2019/04407-4, 2016/07885-1, 2016/20633-6]; CNPq [301354/2019-7]; CAPES [001]

    Keywords: Lactone; Isolinderanolide E; DPPE; Monolayers; Air-water interface

    A long-tail lactone, named isolinderanolide E, was obtained from Nectandra oppositifolia and incorporated in Langmuir monolayers of dipalmitoyl-phosphoethanolamine (DPPE) as a model of microbial membranes. The compound was dissolved in chloroform and mixed with DPPE to provide mixed solutions spread on the air-water interface. After solvent evaporation, mixed monolayers were formed, and surface pressure-area isotherms, dilatational rheology, Brewster angle microscopy (BAM), and infrared spectroscopy were employed to characterize the prodrug-membrane interactions. Isolinderanolide E expanded DPPE monolayers, denoting repulsive interactions. At 30 mN/m, the monolayer presented higher viscoelastic and in-plane elasticity parameters and an increased ratio of all-trans/gauche conformers of the alkyl chains, confirming molecular order. Morphology of the monolayer was analyzed by BAM, which revealed a more homogeneous distribution of Isolinderanolide E along the DPPE monolayer than the prodrug directly spread at the interface, which tends to aggregate. A molecular model proposing the molecular orientation of the amphiphilic drug is presented and explained by the distortion of the alkyl chains as well as by viscoelastic changes. In conclusion, the prodrug changes the thermodynamic, rheological, morphological, and structural properties of the DPPE monolayer, which may be essential to understand, at the molecular level, the action of bioactives in selected membrane models.
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