High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes
about
B cell activation involves nanoscale receptor reorganizations and inside-out signaling by SykThe role of insulin-like growth factor binding protein-3 in the breast cancer cell response to DNA-damaging agentsPartitioning of Thy-1, GM1, and cross-linked phospholipid analogs into lipid rafts reconstituted in supported model membrane monolayers.Lipid rafts, cholesterol, and the brainDetergent-resistant membranes and the protein composition of lipid raftsTetraspanins and Transmembrane Adaptor Proteins As Plasma Membrane Organizers-Mast Cell CaseA critical survey of methods to detect plasma membrane raftsA fluorescent glycolipid-binding peptide probe traces cholesterol dependent microdomain-derived trafficking pathwaysProbing membrane protein interactions with their lipid raft environment using single-molecule tracking and Bayesian inference analysisLipids and membrane microdomains in HIV-1 replicationHeterotrimeric G proteins precouple with G protein-coupled receptors in living cells.Human connexin26 and connexin30 form functional heteromeric and heterotypic channelsCross-species sequence analysis reveals multiple charged residue-rich domains that regulate nuclear/cytoplasmic partitioning and membrane localization of a kinase anchoring protein 12 (SSeCKS/Gravin)Characterization of cholesterol-sphingomyelin domains and their dynamics in bilayer membranesCaveolae/lipid rafts in fibroblast-like synoviocytes: ectopeptidase-rich membrane microdomainsBinding of cross-linked glycosylphosphatidylinositol-anchored proteins to discrete actin-associated sites and cholesterol-dependent domainsGPI anchoring leads to sphingolipid-dependent retention of endocytosed proteins in the recycling endosomal compartment.Cholesterol decreases the interfacial elasticity and detergent solubility of sphingomyelinsCooperation between engulfment receptors: the case of ABCA1 and MEGF10Nanosecond fluorescence resonance energy transfer-fluorescence lifetime imaging microscopy to localize the protein interactions in a single living cell.Confocal FRET microscopy to measure clustering of ligand-receptor complexes in endocytic membranes.Automated selection of regions of interest for intensity-based FRET analysis of transferrin endocytic trafficking in normal vs. cancer cellsDopamine D3 receptor inhibits the ubiquitin-specific peptidase 48 to promote NHE3 degradation.Non-invasive in vivo imaging of near infrared-labeled transferrin in breast cancer cells and tumors using fluorescence lifetime FRET.Three-Color FRET expands the ability to quantify the interactions of several proteins involved in actin filament nucleation.Intensity range based quantitative FRET data analysis to localize protein molecules in live cell nuclei.Issues in confocal microscopy for quantitative FRET analysis.Cholesterol promotes hemifusion and pore widening in membrane fusion induced by influenza hemagglutinin.Differently anchored influenza hemagglutinin mutants display distinct interaction dynamics with mutual rafts.Receptor complexes cotransported via polarized endocytic pathways form clusters with distinct organizations.PIP2 signaling in lipid domains: a critical re-evaluation.Raft composition at physiological temperature and pH in the absence of detergents.R-Ras regulates beta1-integrin trafficking via effects on membrane ruffling and endocytosis.Triggering role of acid sphingomyelinase in endothelial lysosome-membrane fusion and dysfunction in coronary arteries.Membrane raft organization is more sensitive to disruption by (n-3) PUFA than nonraft organization in EL4 and B cells.Dynamic caveolae exclude bulk membrane proteins and are required for sorting of excess glycosphingolipids.Exclusion of lipid rafts and decreased mobility of CD94/NKG2A receptors at the inhibitory NK cell synapse.Role of cholesterol in human immunodeficiency virus type 1 envelope protein-mediated fusion with host cellsZipper-like internalization of Dr-positive Escherichia coli by epithelial cells is preceded by an adhesin-induced mobilization of raft-associated molecules in the initial step of adhesion.Protein interaction quantified in vivo by spectrally resolved fluorescence resonance energy transfer
P2860
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P2860
High-resolution FRET microscopy of cholera toxin B-subunit and GPI-anchored proteins in cell plasma membranes
description
2000 nî lūn-bûn
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2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
High-resolution FRET microscop ...... teins in cell plasma membranes
@ast
High-resolution FRET microscop ...... teins in cell plasma membranes
@en
High-resolution FRET microscop ...... teins in cell plasma membranes
@nl
type
label
High-resolution FRET microscop ...... teins in cell plasma membranes
@ast
High-resolution FRET microscop ...... teins in cell plasma membranes
@en
High-resolution FRET microscop ...... teins in cell plasma membranes
@nl
prefLabel
High-resolution FRET microscop ...... teins in cell plasma membranes
@ast
High-resolution FRET microscop ...... teins in cell plasma membranes
@en
High-resolution FRET microscop ...... teins in cell plasma membranes
@nl
P2093
P2860
P356
P1476
High-resolution FRET microscop ...... teins in cell plasma membranes
@en
P2093
A K Kenworthy
N Petranova
P2860
P304
P356
10.1091/MBC.11.5.1645
P577
2000-05-01T00:00:00Z