Phase Separation of Lipid Microdomains Controlled by Polymerized Lipid Bilayer Matrices

• Published in: Langmuir Vol. 26; no. 6; pp. 4126 - 4129
• Main Authors: Okazaki, Takashi, Tatsu, Yoshiro, Morigaki, Kenichi
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 16.03.2010
• Subjects: Biological Interfaces: Biocolloids, Biomolecular and Biomimetic Materials; Chemistry; Colloidal state and disperse state; Exact sciences and technology; General and physical chemistry; Lipid Bilayers; Membranes; Microscopy, Fluorescence; Phospholipids - chemistry; Polymers - chemistry; Surface physical chemistry; Vesicle; Self assembly; Growth; Ternary mixture; Phospholipid; Polymerization; Lipids; Polymer; Bilayer; Cholesterol; Protein; Solid; Design; Thickness; Geometry; Substrate; Liquid; Phase separation; Membrane; Models
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la9032892

We developed a micropatterned model biological membrane on a solid substrate that can induce phase separation of lipid microdomains in a designed geometry. Micropatterned lipid bilayers were generated by the photolithographic polymerization of a diacetylene phospholipid, 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DiynePC). By changing the UV dose for the photopolymerization, we could modulate the coverage of the surface by the polymeric bilayer domains. After removing nonpolymerized DiynePC, natural phoshoplipid membranes were incorporated into the micropatterned polymeric bilayer matrix by a self-assembly process (vesicle fusion). As we incorporated a ternary lipid mixture of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), sphingomyelin (SM), and cholesterol (Chol) (1:1:1), liquid ordered domains (Lo: rich in SM and Chol) were accumulated in the polymer free regions, whereas liquid disordered domains (Ld: rich in DOPC) preferentially participated into the partially polymeric bilayer regions. It was postulated that Ld domains preferentially came in contact with the polymeric bilayer boundaries because of their lower elastic moduli and a smaller thickness mismatch at the boundary. The effect of polymeric bilayer matrix to hinder the size growth of Lo domains should also be playing an important role. The controlled phase separation should open new possibilities to locally concentrate membrane proteins and other nanometer-sized materials on the substrate by associating them with the lipid microdomains.