Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/10032
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSalvemini, Iyrrien
dc.contributor.authorReid, Jacquelineen
dc.contributor.authorMoens, Pierreen
dc.date.accessioned2012-05-01T16:22:00Z-
dc.date.issued2010-
dc.identifier.citationProceedings of the Australian Physiological Society, v.41, p. 94-94en
dc.identifier.issn0067-2084en
dc.identifier.urihttps://hdl.handle.net/1959.11/10032-
dc.description.abstractThe use of Giant Unilamellar Vesicles (GUVs) composed of fluorescently labelled lipid analogues has become an increasing popular model to study both structural and complex biophysical properties of bilayers. However, there is a common assumption that the number of probes incorporated into the membrane of the GUVs is proportional to the mole fraction (%) of these lipid molecules in the original solvent solution. A commercial confocal laser scanning microscope (Nikon C1) was used to obtain single point fluorescence correlation spectroscopy (FCS) data. The time dependence of the spontaneous fluctuations and the number of molecules in the detection volume (point spread function) was calculated using the autocorrelation function of the fluorescent signals. From these data, the diffusion coefficient (D1)and the number of fluorescent molecules (N) incorporated into the membrane was obtained. We successfully measured the diffusion coefficient of two different labelled lipid analogues (1,1-dioctadecyl-3,3,3,3-tetramethylindocarbocyanine perchlorate[DiIC18] and BODIPY TMR-phosphatidylinositol (4,5) bisphosphate[TMR-PI(4,5)P2])incorporated into the membrane of GUVs (Moens, Gratton & Salvemini, 2010). The results obtained for these lipid analogs are in good agreement with previously published data (Golebiewska et al.. 2006; Golebiewska et al.. 2008; Gielen et al.. 2009). We also show that the number of DiIC18molecules incorporated into the membrane of the GUVs (formed by the electroformation method) is in agreement with the expected number of molecules calculated from the mole fraction of the organic stock solution. However, we find that the actual proportion of β-BODIPY-HPC,TR-PI(4,5)P2,and TMR-PI(4,5)P2 incorporated into the bilayer is significantly less than the proportion of these lipids in the organic solvent stock solution. These findings draw attention to the need to quantitatively measure the incorporation of these probes for experiments in which the concentration is of importance to the parameter being investigated.en
dc.languageenen
dc.publisherAustralian Physiological Society (AuPS)en
dc.relation.ispartofProceedings of the Australian Physiological Societyen
dc.relation.ispartofseriesProceedings of the Australian Physiological Societyen
dc.titleMeasuring the incorporation of fluorescently labelled lipid analogues into the membrane of giant unilamellar vesiclesen
dc.typeConference Publicationen
dc.relation.conferenceAuPS/ASB 2010: Joint Annual Meeting of the Australian Physiological Society and Australian Society for Biophysicsen
dc.subject.keywordsAnalytical Biochemistryen
dc.subject.keywordsBiological Physicsen
local.contributor.firstnameIyrrien
local.contributor.firstnameJacquelineen
local.contributor.firstnamePierreen
local.subject.for2008029901 Biological Physicsen
local.subject.for2008060101 Analytical Biochemistryen
local.subject.seo2008970110 Expanding Knowledge in Technologyen
local.subject.seo2008970106 Expanding Knowledge in the Biological Sciencesen
local.profile.schoolSchool of Science and Technologyen
local.profile.schoolSchool of Science and Technologyen
local.profile.emailisalvem2@une.edu.auen
local.profile.emailjreid3@une.edu.auen
local.profile.emailpmoens@une.edu.auen
local.output.categoryE3en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.identifier.epublicationsrecordune-20120501-095126en
local.date.conference28th November - 1st December, 2010en
local.conference.placeAdelaide, Australiaen
local.publisher.placeAustraliaen
local.format.startpage94en
local.format.endpage94en
local.series.issn0067-2084en
local.series.number41en
local.identifier.volume41en
local.contributor.lastnameSalveminien
local.contributor.lastnameReiden
local.contributor.lastnameMoensen
dc.identifier.staffune-id:isalvem2en
dc.identifier.staffune-id:jreid3en
dc.identifier.staffune-id:pmoensen
local.profile.orcid0000-0002-5193-3818en
local.profile.orcid0000-0003-3121-5306en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:10223en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleMeasuring the incorporation of fluorescently labelled lipid analogues into the membrane of giant unilamellar vesiclesen
local.output.categorydescriptionE3 Extract of Scholarly Conference Publicationen
local.relation.urlhttp://aups.org.au/Proceedings/41/94P/en
local.relation.grantdescriptionNHMRC/568301en
local.conference.detailsAuPS/ASB 2010: Joint Annual Meeting of the Australian Physiological Society and Australian Society for Biophysics, Adelaide, Australia, 28th November - 1st December, 2010en
local.search.authorSalvemini, Iyrrien
local.search.authorReid, Jacquelineen
local.search.authorMoens, Pierreen
local.uneassociationUnknownen
local.year.published2010-
local.date.start2010-11-28-
local.date.end2010-12-01-
local.profile.affiliationtypeUnknownen
local.profile.affiliationtypeUnknownen
local.profile.affiliationtypeUnknownen
Appears in Collections:Conference Publication
Files in This Item:
2 files
File Description SizeFormat 
Show simple item record

Page view(s)

1,004
checked on Mar 8, 2023
Google Media

Google ScholarTM

Check


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