Chondroitin sulfate interacts mainly with headgroups in phospholipid monolayers

Autor(es)

Ceridorio, Lucineia F. ^[1] ; Caseli, Luciano ^[1] ; Oliveira, Jr., Osvaldo N. ^[2]

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo, UNIFESP, Inst Environm Chem & Pharmaceut Sci, Diadema, SP - Brazil

^[2] Univ Sao Paulo, Inst Phys Sao Carlos, Sao Carlos, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: COLLOIDS AND SURFACES B-BIOINTERFACES; v. 141, p. 595-601, MAY 1 2016.
• Citações Web of Science: 1

Resumo

Sulfated glycosaminoglycans are precursors of the extracellular matrix used to treat diseases related to blood clotting and degenerative joint diseases. These medical applications have been well established, but the mode of action at the molecular level, which depends on the interaction with cell membranes, is not known in detail. In this study, we investigated the interaction between chondroitin sulfate (CS) and phospholipid monolayers that mimic cell membranes. From surface pressure isotherms and polarization modulated infrared reflection absorption spectroscopy (PM-IRRAS), CS was found to interact mainly with the polar groups of dipalmitoyl phosphatidylcholine (DPPC) and dipalmitoyl phosphatidylglycerol (DPPG), with negligible penetration into the hydrophobic tails and only small changes in monolayer elasticity for the packing corresponding to a real cell membrane. The changes in surface pressure and surface potential isotherms depended on CS concentration and on the time allowed for its adsorption onto the monolayer, which points to a dynamic adsorption-desorption process. The charge of the phospholipid was also relevant, since CS induced order into DPPC monolayers while the opposite occurred for DPPG, according to the PM-IRRAS spectra. In summary, interaction with polar groups is responsible for the CS effects on model cell membranes. (C) 2016 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 13/14262-7 - Filmes nanoestruturados de materiais de interesse biológico
• Beneficiário: Osvaldo Novais de Oliveira Junior
• Modalidade de apoio: Auxílio à Pesquisa - Temático