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Biomimetic liposomes and planar supported bilayers for the assessment of glycodendrimeric porphyrins interaction with an immobilized lectin

Year: 2011

Journal: Biochimica et Biophysica Acta (BBA) - Biomembranes, Volume 1808, Issue 3, March 2011, Pages 656-666, 20110317

Authors: Makky A. 1 2 6, Michel J.P. 1 2 6, Maillard Ph. 3 4 5 6, Rosilio V. 1 3 6

Last authors: V. Rosilio

Organizations: a Univ Paris-Sud 11, UMR 8612, Laboratoire de Physico-chimie des Surfaces, 5 rue Jean-Baptiste Clément, F-92296 Châtenay-Malabry, France b CNRS, UMR 8612, F-92296 Châtenay-Malabry, France c Institut Curie, Centre de Recherche, Bât 110-112, F-91405, Orsay, France d CNRS, UMR 176, F-91405 Orsay, France e Univ Paris-Sud 11, centre universitaire, F-91405 Orsay, France f CNRS GDR 3049 PHOTOMED, France

Country: France

Photodynamic therapy is a potentially efficient treatment for various solid tumours, among which retinoblastoma. Its efficacy depends on the preferential accumulation of photosensitizers in the malignant tissues and their accessibility to light. The specificity of drugs for retinoblastoma cells can be improved by targeting a mannose receptor overexpressed at their surface. With the aim of assessing the recognition of newly synthesized glycodendrimeric porphyrins by such receptors, we have built and characterized an original synthetic biomimetic membrane having similar lipidic composition to that of the retinal cell membranes and bearing Concanavalin A, as a model of the mannose receptor. The interaction of the porphyrin derivatives with liposomes and supported planar bilayers has been studied by dynamic light scattering and quartz crystal microbalance with dissipation monitoring (QCM -D). Only mannosylated porphyrins interacted significantly with the membrane model. The methodology used proved to be efficient for the selection of potentially active compounds.