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Spatiotemporal Kinetics of Supported Lipid Bilayer Formation on Glass via Vesicle Adsorption and Rupture
被引:22
|作者:
Mapar, Mokhtar
[1
]
Yoemetsa, Silver
[1
]
Pace, Hudson
[1
]
Zhdanov, Vladimir P.
[1
,2
]
Agnarsson, Bjorn
[1
]
Hook, Fredrik
[1
]
机构:
[1] Chalmers Univ Technol, Dept Phys, Div Biol Phys, S-41296 Gothenburg, Sweden
[2] Russian Acad Sci, Boreskov Inst Catalysis, Novosibirsk 630090, Russia
来源:
基金:
瑞典研究理事会;
关键词:
QUARTZ-CRYSTAL MICROBALANCE;
ATOMIC-FORCE MICROSCOPY;
PROTEIN MOBILITY;
CELL-MEMBRANES;
QCM-D;
PATCHES;
FUSION;
MICA;
AFM;
D O I:
10.1021/acs.jpclett.8b02092
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Supported lipid bilayers (SLBs) represent one of the most popular mimics of the cell membrane. Herein, we have used total internal reflection fluorescence microscopy for in-depth characterization of the vesicle-mediated SLB formation mechanism on a common silica-rich substrate, borosilicate glass. Fluorescently labeling a subset of vesicles allowed us to monitor the adsorption of individual labeled vesicles, resolve the onset of SLB formation from small seeds of SLB patches, and track their growth via SLB-edge-induced autocatalytic rupture of adsorbed vesicles. This made it possible to perform the first quantitative measurement of the SLB front velocity, which is shown to increase up to 1 order of magnitude with time. This effect can be classified as dramatic because in many other physical, chemical, or biological kinetic processes the front velocity is either constant or decreasing with time. The observation was successfully described with a theoretical model and Monte Carlo simulations implying rapid local diffusion of lipids upon vesicle rupture.
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页码:5143 / 5149
页数:13
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