Full metadata record

DC Field Value Language
dc.contributor.authorRyu, Yong-Sang-
dc.contributor.authorYun, Hansik-
dc.contributor.authorChung, Taerin-
dc.contributor.authorSuh, Jeng-Hun-
dc.contributor.authorKim, Sungho-
dc.contributor.authorLee, Kyookeun-
dc.contributor.authorWittenberg, Nathan J.-
dc.contributor.authorOh, Sang-Hyun-
dc.contributor.authorLee, Byoungho-
dc.contributor.authorLee, Sin-Doo-
dc.date.accessioned2024-01-19T19:02:43Z-
dc.date.available2024-01-19T19:02:43Z-
dc.date.created2021-09-05-
dc.date.issued2019-10-01-
dc.identifier.issn0956-5663-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/119475-
dc.description.abstractA 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.-
dc.languageEnglish-
dc.publisherELSEVIER ADVANCED TECHNOLOGY-
dc.subjectMEMBRANE-
dc.subjectMODEL-
dc.subjectPROTEINS-
dc.subjectPHASE-
dc.subjectMANIPULATION-
dc.subjectDIFFUSION-
dc.subjectDOMAINS-
dc.subjectSENSORS-
dc.subjectBINDING-
dc.titleKinetics of lipid raft formation at lipid monolayer-bilayer junction probed by surface plasmon resonance-
dc.typeArticle-
dc.identifier.doi10.1016/j.bios.2019.111568-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOSENSORS & BIOELECTRONICS, v.142-
dc.citation.titleBIOSENSORS & BIOELECTRONICS-
dc.citation.volume142-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000487175000088-
dc.identifier.scopusid2-s2.0-85070813812-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.type.docTypeArticle-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusPHASE-
dc.subject.keywordPlusMANIPULATION-
dc.subject.keywordPlusDIFFUSION-
dc.subject.keywordPlusDOMAINS-
dc.subject.keywordPlusSENSORS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordAuthorLipid raft-
dc.subject.keywordAuthorLipid monolayer-bilayer junction-
dc.subject.keywordAuthorReal-time-
dc.subject.keywordAuthorSurface plasmon resonance-
dc.subject.keywordAuthorOptical sensors-
dc.subject.keywordAuthorLipid-lipid interaction-
Appears in Collections:
KIST Article > 2019
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE