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Patterned domains of supported phospholipid bilayer using microcontact printing of Pll-g-PEG molecules

Year: 2012

Journal: Colloids and Surfaces B: Biointerfaces, Volume 89, 1 January 2012, Pages 188-195, 20111207

Authors: Chalmeau J. 1 2, le Grimellec C 3, Sternick J 4, Vieu C 1 2

Last authors: Christophe Vieu

Organizations: 1 CNRS; LAAS; 7 Avenue du Colonel Roche, F-31077 Toulouse, France 2 Université de Toulouse; UPS, INSA, INP, ISAE; LAAS; F-31077 Toulouse, France 3 INSERM, Unité 554, 29 rue de Navacelles, 34090 Montpellier, France 4 Mansfield University, Department of Biology, 16933 Mansfield, USA

Country: France, USA, US, United States, United States of America, America

In this work, we propose a reliable microcontact printing (μCP) process for generating Patterned Supported Phospholipids Bilayer (P-SPB) confined by Poly-l-(lysine)-grafted-polyethylene(glycol) (Pll-g-PEG) molecular barriers. The efficiency of Pll-g-PEG for inhibiting the fusion process of incubated liposome was first analyzed by Quartz Micro Balance ( QCM ) measurements. The quality and stability of Pll-g-PEG patterns were then both verified by fluorescence microscopy and Atomic Force Microscopy (AFM) in liquid media. The micro domains of P-SPB produced were stable in liquid environment during several weeks and also during AFM imaging. This exceptional stability is a clear improvement compared to previous studies involving proteins as confinement barriers.