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Glycolipid–cholesterol monolayers: Towards a better understanding of the interaction between the membrane components

Year: 2011

Journal: Biochimica et Biophysica Acta, 1808 (10), 2466-2476, 20131009

Authors: Beata Korchowiec, Jacek Korchowiec, Masakatsu Hato, Ewa Rogalska

Organizations: Department of Physical Chemistry and Electrochemistry, Faculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland; Department of Theoretical Chemistry, Faculty of Chemistry, Jagiellonian University, ul. R. Ingardena 3, 30-060 Krakow, Poland; RIKEN Systems and Structural Biology Center, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa-230-0045, Japan; Nanotechnology Research Institute, AIST. Tsukuba Central-5, Higashi 1-1-1, Tsukuba, Ibaraki 305-8565, Japan; Equipe GEVSM, Structure et Réactivité des Systèmes Moléculaires Complexes, UMR 7565 Nancy Université/CNRS, BP 239, 54506 Vandoeuvre-lès-Nancy cedex, France

In this work, the interaction between a synthetic analog of archaeal lipids and cholesterol was studied using Langmuir technique. The lipid, β-Mal3O(C16 + 4)2, contained phytanyl chains attached via two ether bonds to the sn-2 carbon of the glycerol backbone. The preliminary studies showed that monolayers formed with the pure lipid have a liquid-like character; here, a hypothesis that admixing cholesterol to β-Mal3O(C16 + 4)2 could confer a higher rigidity on the films was tested. To check this proposal, two-dimensional miscibility of cholesterol and β-Mal3O(C16 + 4)2 in monomolecular films was studied using surface pressure and surface potential measurements, as well as Brewster angle microscopy and polarization-modulation infrared reflection absorption spectroscopy. The stability of the monomolecular films was evaluated based on thermodynamics of mixing of cholesterol and β-Mal3O(C16 + 4)2. Atomic level information concerning the orientation of molecules and the degree of hydration of polar headgroups was obtained from molecular dynamics simulations.