2016
DOI: 10.1016/j.bpj.2015.11.1143
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Characterization of CEACAM1 and Lipid Raft Nanoclustering, Association and Structure by dSTORM and homo-FRET Imaging

Abstract: Using an agarose hydration technique for protein incorporation into vesicular bilayers, we elucidate the effects of membrane composition and ordering on G Protein Coupled Receptors (GPRCs). We successfully incorporate GPCRs into model membranes in the form of giant unilamellar proteinvesicles (GUPs). Using this completely in vitro platform we observe that the functional rate of the human serotonin receptor, GPCR 5-HT 1A , and the A 2 a Adenosine GPCR is dependent on membrane composition and ordering. We use BO… Show more

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“…Furthermore, through increasing the local concentration of CEACAM1 monomers, clustering is promoted. Thus, the presence of lipid raft regions in the Cell4D models creates a spatial dynamic that matches the known observation of CEACAM1 clusters being primarily monomeric within lipid rafts, and dimeric CEACAM1 being localized in lipid-disordered regions outside of rafts [33].…”
Section: Discussionsupporting
confidence: 71%
“…Furthermore, through increasing the local concentration of CEACAM1 monomers, clustering is promoted. Thus, the presence of lipid raft regions in the Cell4D models creates a spatial dynamic that matches the known observation of CEACAM1 clusters being primarily monomeric within lipid rafts, and dimeric CEACAM1 being localized in lipid-disordered regions outside of rafts [33].…”
Section: Discussionsupporting
confidence: 71%
“…Furthermore, through increasing the local concentration of CEACAM1 monomers, clustering is promoted. Thus, the presence of lipid raft regions in the Cell4D models creates a spatial dynamic that matches the known observation of CEACAM1 clusters being primarily monomeric within lipid rafts, and dimeric CEACAM1 being localized in lipid-disordered regions outside of rafts [32].…”
Section: Discussionsupporting
confidence: 71%