Colloid supported lipid bilayers for self-assembly. Issue 6 (19th December 2018)

• Record Type: Journal Article
• Authors: Rinaldin, Melissa; Verweij, Ruben W.; Chakraborty, Indrani; Kraft, Daniela J.
• Is Part Of: Soft matter. Volume 15:Issue 6(2019)
• Page Start: 1345
• Page End: 1360
• Publication Date: 2018-12-19
• Subjects: Soft condensed matter -- Periodicals; 530.413
• DOI: 10.1039/c8sm01661e
• Languages: English
• ISSNs: 1744-683X

Abstract

Abstract : Careful tuning of the experimental parameters involved in preparing colloid supported lipid bilayers enables the self-assembly of flexible structures. Abstract : The use of colloid supported lipid bilayers (CSLBs) has recently been extended to create colloidal joints, that enable the assembly of structures with internal degrees of flexibility, and to study lipid membranes on curved and closed geometries. These novel applications of CSLBs rely on previously unappreciated properties: the simultaneous fluidity of the bilayer, lateral mobility of inserted (linker) molecules and colloidal stability. Here we characterize every step in the manufacturing of CSLBs in view of these requirements using confocal microscopy and fluorescence recovery after photobleaching (FRAP). Specifically, we have studied the influence of different particle properties (roughness, surface charge, chemical composition, polymer coating) on the quality and mobility of the supported bilayer. We find that the insertion of lipopolymers in the bilayer can affect its homogeneity and fluidity. We improve the colloidal stability by inserting lipopolymers or double-stranded inert DNA into the bilayer. We include surface-mobile DNA linkers and use FRAP to characterize their lateral mobility both in their freely diffusive and bonded state. Finally, we demonstrate the self-assembly of flexibly linked structures from the CSLBs modified with surface-mobile DNA linkers. Our work offers a collection of experimental tools for working with CSLBs in applications ranging from controlled bottom-up self-assembly to model membrane studies.