<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao J</submitter><funding>NIGMS NIH HHS</funding><pagination>2764-76</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2701629</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>1768(11)</volume><pubmed_abstract>We have undertaken a series of experiments to examine the behavior of individual components of cell membranes. Here we report an initial stage of these experiments, in which the properties of a chemically simple lipid mixture are carefully mapped onto a phase diagram. Four different experimental methods were used to establish the phase behavior of the 3-component mixture DSPC/DOPC/chol: (1) confocal fluorescence microscopy observation of giant unilamellar vesicles, GUVs; (2) FRET from perylene to C20:0-DiI; (3) fluorescence of dilute dyes C18:2-DiO and C20:0-DiI; and (4) wide angle X-ray diffraction. This particular 3-component mixture was chosen, in part, for a high level of immiscibility of the components in order to facilitate solving the phase behavior at all compositions. At 23 degrees C, a large fraction of the possible compositions for this mixture give rise to a solid phase. A region of 3-phase coexistence of {Lalpha+Lbeta+Lo} was detected and defined based on a combination of fluorescence microscopy of GUVs, FRET, and dilute C20:0-DiI fluorescence. At very low cholesterol concentrations, the solid phase is the tilted-chain phase Lbeta'. Most of the phase boundaries have been determined to be within a few percent of the composition. Measurements of the perturbations of the boundaries of this accurate phase diagram could serve as a means to understand the behaviors of a range of added lipids and proteins.</pubmed_abstract><journal>Biochimica et biophysica acta</journal><pubmed_title>Phase studies of model biomembranes: complex behavior of DSPC/DOPC/cholesterol.</pubmed_title><pmcid>PMC2701629</pmcid><funding_grant_id>T32 GM008267</funding_grant_id><funding_grant_id>T32 GM008267-17</funding_grant_id><funding_grant_id>1 T32 GM08267</funding_grant_id><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Feigenson GW</pubmed_authors><pubmed_authors>Mills TT</pubmed_authors><pubmed_authors>Costanza G</pubmed_authors><pubmed_authors>Huang G</pubmed_authors><pubmed_authors>Klawitter P</pubmed_authors><pubmed_authors>Heberle FA</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase studies of model biomembranes: complex behavior of DSPC/DOPC/cholesterol.</name><description>We have undertaken a series of experiments to examine the behavior of individual components of cell membranes. Here we report an initial stage of these experiments, in which the properties of a chemically simple lipid mixture are carefully mapped onto a phase diagram. Four different experimental methods were used to establish the phase behavior of the 3-component mixture DSPC/DOPC/chol: (1) confocal fluorescence microscopy observation of giant unilamellar vesicles, GUVs; (2) FRET from perylene to C20:0-DiI; (3) fluorescence of dilute dyes C18:2-DiO and C20:0-DiI; and (4) wide angle X-ray diffraction. This particular 3-component mixture was chosen, in part, for a high level of immiscibility of the components in order to facilitate solving the phase behavior at all compositions. At 23 degrees C, a large fraction of the possible compositions for this mixture give rise to a solid phase. A region of 3-phase coexistence of {Lalpha+Lbeta+Lo} was detected and defined based on a combination of fluorescence microscopy of GUVs, FRET, and dilute C20:0-DiI fluorescence. At very low cholesterol concentrations, the solid phase is the tilted-chain phase Lbeta'. Most of the phase boundaries have been determined to be within a few percent of the composition. Measurements of the perturbations of the boundaries of this accurate phase diagram could serve as a means to understand the behaviors of a range of added lipids and proteins.</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Nov</publication><modification>2020-10-29T14:32:47Z</modification><creation>2019-03-27T00:23:10Z</creation></dates><accession>S-EPMC2701629</accession><cross_references><pubmed>17825247</pubmed><doi>10.1016/j.bbamem.2007.07.008</doi></cross_references></HashMap>