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Layer-by-Layer PMIRRAS Characterization of DMPC Bilayers Deposited on a Au(111) Electrode Surface

Year: 2006

Journal: Langmuir, 2006, 22 (25), pp 10365–10371, 20111221

Authors: Nuria Garcia-Araez, Christa L. Brosseau, Paramaconi Rodriguez, and Jacek Lipkowski

Organizations: Department of Chemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1, and Departamento de Química Física, Universidad de Alicante, Apart 99, E-03080 Alicante, Spain

A combination of Langmuir−Blodgett and Langmuir−Schaefer techniques was employed to deposit 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) bilayers at a gold electrode surface. One leaflet consisted of hydrogen-substituted acyl chains, and the second leaflet was composed of molecules with deuterium-substituted acyl chains. This architecture allowed for layer-by-layer analysis of the structure of the bilayer. Photon polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS) was used to determine the conformation and orientation of the acyl chains of DMPC molecules in the individual leaflets as a function of the potential applied to the gold electrode. The bilayer is adsorbed onto the metal surface when the field applied to the membrane does not exceed 108 V/m. When adsorbed, the bottom leaflet is in contact with a hydrophobic metal surface, and the top leaflet is interacting with the aqueous solution. The asymmetry of the environment has an effect on the orientation of the DMPC molecules in each leaflet. The tilt angle of the acyl chains of the DMPC molecules in the bottom leaflet that is in contact with the gold is 10° smaller than that observed for the top leaflet that is exposed to the solution. These studies provide direct evidence that the structure of a phospholipid bilayer deposited at an electrode surface is affected by interaction with the metal.