Kinetics of lipid raft formation at lipid monolayer-bilayer junction probed by surface plasmon resonance

Authors
Ryu, Yong-SangYun, HansikChung, TaerinSuh, Jeng-HunKim, SunghoLee, KyookeunWittenberg, Nathan J.Oh, Sang-HyunLee, ByounghoLee, Sin-Doo
Issue Date
2019-10-01
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Citation
BIOSENSORS & BIOELECTRONICS, v.142
Abstract
A label-free, non-dispruptive, and real-time analytical device to monitor the dynamic features of biomolecules and their interactions with neighboring molecules is an essential prerequisite for biochip- and diagonostic assays. To explore one of the central questions on the lipid-lipid interactions in the course of the liquid-ordered (l(o)) domain formation, called rafts, we developed a method of reconstituting continuous but spatially heterogeneous lipid membrane platforms with molayer-bilayer juntions (MBJs) that enable to form the l(o) domains in a spatiotemporally controlled manner. This allows us to detect the time-lapse dynamics of the lipid-lipid interactions during raft formation and resultant membrane phase changes together with the raft-associated receptor-ligand binding through the surface plasmon resonance (SPR). For cross-validation, using epifluorescence microscopy, we demonstrated the underlying mechanisms for raft formations that the infiltration of cholesterols into the sphingolipid-enriched domains plays a crucial roles in the membrane phase-separation. Our membrane platform, being capable of monitoring dynamic interactions among lipids and performing the systematic optical analysis, will unveil physiological roles of cholesterols in a variety of biological events.
Keywords
MEMBRANE; MODEL; PROTEINS; PHASE; MANIPULATION; DIFFUSION; DOMAINS; SENSORS; BINDING; MEMBRANE; MODEL; PROTEINS; PHASE; MANIPULATION; DIFFUSION; DOMAINS; SENSORS; BINDING; Lipid raft; Lipid monolayer-bilayer junction; Real-time; Surface plasmon resonance; Optical sensors; Lipid-lipid interaction
ISSN
0956-5663
URI
https://pubs.kist.re.kr/handle/201004/119475
DOI
10.1016/j.bios.2019.111568
Appears in Collections:
KIST Article > 2019
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