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• W2048953765 endingPage "254" @default.
• W2048953765 startingPage "249" @default.
• W2048953765 abstract "Lipid rafts are plasma membrane microdomains enriched in sphingolipids and cholesterol. These domains have been suggested to serve as platforms for various cellular events, such as signaling and membrane trafficking. However, little is known about the distribution and dynamics of lipids in these microdomains. Here we report investigations carried out using recently developed probes for the lipid components of lipid rafts: lysenin, a sphingomyelin-binding protein obtained from the coelomic fluid of the earthworm Eisenia foetida; and the fluorescein ester of poly(ethyleneglycol) cholesteryl ether (fPEG-Chol), which partitions into cholesterol-rich membranes. Lysenin reveals that the organization of sphingomyelin differs between different cell types and even between different membrane domains within the same cell. When added to live cells, fPEG-Chol is distributed exclusively on the outer leaflet of the plasma membrane and is clustered dynamically upon activation of receptor signaling. The surface-bound fPEG-Chol is slowly internalized via a clathrin-independent pathway into endosomes with lipid raft markers." @default.
• W2048953765 created "2016-06-24" @default.
• W2048953765 creator A5085926636 @default.
• W2048953765 date "2005-03-01" @default.
• W2048953765 modified "2023-09-23" @default.
• W2048953765 title "Imaging Lipid Rafts" @default.
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• W2048953765 doi "https://doi.org/10.1093/jb/mvi041" @default.
• W2048953765 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/15809325" @default.
• W2048953765 hasPublicationYear "2005" @default.
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