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Relationship Between Vesicle Size and Steric Hindrance Influences Vesicle Rupture on Solid Supports Full article

Journal PCCP: Physical Chemistry Chemical Physics
ISSN: 1463-9076 , E-ISSN: 1463-9084
Output data Year: 2016, Volume: 18, Number: 4, Pages: 3065-3072 Pages count : 8 DOI: 10.1039/c5cp06786c
Tags QUARTZ-CRYSTAL MICROBALANCE; ATOMIC-FORCE MICROSCOPY; LIPID-BILAYER FORMATION; SURFACE-PLASMON RESONANCE; UNILAMELLAR VESICLES; OSMOTIC-PRESSURE; ADSORPTION; MEMBRANES; ADHESION; EXTRUSION
Authors Jackman Joshua A. 1,2 , Kim Min Chul 1,2 , Zhdanov Vladimir P. 1,2,4 , Cho Nam-Joon 1,2,3
Affiliations
1 School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue 639798, Singapore
2 Centre for Biomimetic Sensor Science, Nanyang Technological University, 50 Nanyang Drive 637553, Singapore
3 School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive 637459, Singapore
4 Boreskov Institute of Catalysis, Russian Academy of Sciences, Novosibirsk 630090, Russia

Funding (1)

1 National Research Foundation of Singapore NRF-NRFF2011-01

Abstract: Phospholipid assemblies on solid supports mimic the cell membrane, and provide a platform to study membrane biology. Among the different types of model membranes, the planar bilayer is a two-dimensional lipid bilayer sheet that can be formed by the adsorption and spontaneous rupture of vesicles. The formation process is influenced by the interactions between vesicles and the solid support as well as between vesicles. On silicon oxide, which is a commonly used solid support, vesicles typically adsorb until reaching a critical coverage and then spontaneous rupture begins. Although it is generally understood that spontaneous rupture leads to planar bilayer formation, oversaturation of vesicles at the critical coverage can hinder the whole process due to a steric factor. To date, the role of this factor has been scrutinized only in relation to temperature, and the influence of additional parameters remains to be elucidated. In this work, we have investigated how vesicle size and corresponding steric constraints influence the kinetics of vesicle adsorption and rupture and, more specifically, how the state of adsorbed vesicles after fusion depends on the vesicle size. Using quartz crystal microbalance-dissipation (QCM-D) and fluorescence recovery after photobleaching (FRAP), we characterized the adsorption kinetics of vesicles onto silicon oxide and the lateral mobility of solid-supported lipid assemblies. While the vesicle adsorption kinetics were diffusion-limited up to the onset of vesicle rupture, the extent of rupture depended on vesicle size and it was observed that larger vesicles are more prone to steric effects than smaller vesicles. We discuss this finding in terms of the structural transformation from adsorbed vesicles to a planar bilayer, including how the interplay of thermodynamic, kinetic and steric factors can affect vesicle rupture on solid supports
Cite: Jackman J.A. , Kim M.C. , Zhdanov V.P. , Cho N-J.
Relationship Between Vesicle Size and Steric Hindrance Influences Vesicle Rupture on Solid Supports
PCCP: Physical Chemistry Chemical Physics. 2016. V.18. N4. P.3065-3072. DOI: 10.1039/c5cp06786c WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Nov 6, 2015
Accepted: Dec 15, 2015
Published online: Dec 15, 2015
Published print: Jan 28, 2016
Identifiers:
Web of science: WOS:000369506000085
Scopus: 2-s2.0-84955267590
Elibrary: 26728066
Chemical Abstracts: 2015:2010945
Chemical Abstracts (print): 164:207595
OpenAlex: W2199875511
Citing:
DB Citing
Web of science 22
Scopus 22
Elibrary 22
OpenAlex 28
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