Cholesterol is required for surface transport of influenza virus hemagglutinin.
about
Cholesterol binds to synaptophysin and is required for biogenesis of synaptic vesiclesAssociation of gamma-secretase with lipid rafts in post-Golgi and endosome membranes.Partitioning of Thy-1, GM1, and cross-linked phospholipid analogs into lipid rafts reconstituted in supported model membrane monolayers.Oxysterol binding protein-related Protein 9 (ORP9) is a cholesterol transfer protein that regulates Golgi structure and functionExtraction of cholesterol with methyl-beta-cyclodextrin perturbs formation of clathrin-coated endocytic vesiclesVirus entry, assembly, budding, and membrane raftsRole of KIFC3 motor protein in Golgi positioning and integrationGalectin-4 and sulfatides in apical membrane trafficking in enterocyte-like cellsCritical role for cholesterol in Lyn-mediated tyrosine phosphorylation of FcepsilonRI and their association with detergent-resistant membranesKIFC3, a microtubule minus end-directed motor for the apical transport of annexin XIIIb-associated Triton-insoluble membranesSpatial partitioning of secretory cargo from Golgi resident proteins in live cells.MHC class II association with lipid rafts on the antigen presenting cell surfaceBinding Dynamics of Hepatitis C Virus' NS5A Amphipathic Peptide to Cell and Model MembranesDissecting the role of the golgi complex and lipid rafts in biosynthetic transport of cholesterol to the cell surface.Influenza virus hemagglutinin concentrates in lipid raft microdomains for efficient viral fusion.Membrane accumulation of influenza A virus hemagglutinin triggers nuclear export of the viral genome via protein kinase Calpha-mediated activation of ERK signaling.Plasma membrane proton ATPase Pma1p requires raft association for surface delivery in yeast.Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast.Saccharomyces cerevisiae Na+/H+ antiporter Nha1p associates with lipid rafts and requires sphingolipid for stable localization to the plasma membrane.Multi-Omics Studies towards Novel Modulators of Influenza A Virus-Host InteractionSNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosisNa+-H+ exchanger 3 (NHE3) is present in lipid rafts in the rabbit ileal brush border: a role for rafts in trafficking and rapid stimulation of NHE3Cholesterol depletion reduces apical transport capacity in epithelial Madin-Darby canine kidney cellsNanotechnology-Based Drug Delivery Systems for Melanoma Antitumoral Therapy: A ReviewIntegrin leukocyte function-associated antigen-1-mediated cell binding can be activated by clustering of membrane raftsRole of Src-induced dynamin-2 phosphorylation in caveolae-mediated endocytosis in endothelial cellsP2X3 receptor localizes into lipid rafts in neuronal cellsLipid domain structure of the plasma membrane revealed by patching of membrane componentsCholesterol promotes hemifusion and pore widening in membrane fusion induced by influenza hemagglutinin.Cholesterol is required for efficient endoplasmic reticulum-to-Golgi transport of secretory membrane proteins.Lipid rafts enriched in monosialylGb5Cer carrying the stage-specific embryonic antigen-4 epitope are involved in development of mouse preimplantation embryos at cleavage stage.Human cytomegalovirus glycoprotein B contains autonomous determinants for vectorial targeting to apical membranes of polarized epithelial cells.Effects of methylcyclodextrin on lysosomes.Cell polarity and PIN protein positioning in Arabidopsis require STEROL METHYLTRANSFERASE1 function.Complex gangliosides are apically sorted in polarized MDCK cells and internalized by clathrin-independent endocytosis.Lipid rafts and clathrin cooperate in the internalization of PrP in epithelial FRT cellsA clathrin independent macropinocytosis-like entry mechanism used by bluetongue virus-1 during infection of BHK cells.Golgi sorting regulates organization and activity of GPI proteins at apical membranesInward cholesterol gradient of the membrane system in P. falciparum-infected erythrocytes involves a dilution effect from parasite-produced lipids.Membrane raft association is a determinant of plasma membrane localization
P2860
Q22011017-AF8707FE-66DD-4A6E-AD2D-5D2D2BA53BAAQ24532064-FBEDA08B-DADC-4549-BC8C-C8441C912B1EQ24555205-0CDD082B-BA5D-4E91-8813-4B6E1EFAF34CQ24647008-B51DF126-AAA2-4471-8AD1-B9D47AA6687AQ24657869-1ABBE81F-835E-4669-A6AE-C9963FE1587EQ24673161-6FE43C74-02CC-4FCB-BC0E-D51C29CB7D3EQ24673774-13A3A59D-0884-4EC3-842E-7434C694DCE4Q24678274-DA0E8F3F-A4C0-437E-B167-9FA9F96F4757Q24681993-C97C321A-358C-4C68-B805-BC3285F2D396Q24685497-D9EF4C98-F9E1-447C-9BE0-5924FA454EA2Q24794775-179D1B07-73F5-4A5B-92C3-5EB27B07166EQ27008954-21F20463-31A9-4B4F-8527-DA140764277CQ27480337-CF004741-4242-44CA-9C63-0D8BCBB7FA29Q27863672-79A2AA61-D23D-49BD-847F-9F94FDF6885EQ27863777-FDE8E84C-267F-4681-A6EB-E1B566FEE02EQ27863918-C344D999-C206-49C9-B131-9DDACA69CAC5Q27932251-1F292554-BDCC-4371-B22D-7AE568B280D6Q27932650-FB195C0A-077C-4E33-A09E-28920612AEC5Q27939067-6886C0D7-2599-4A7A-B5FF-EBB641A3C19EQ28073474-E68D12BD-F089-4D17-8256-9DDFA4BDDAF4Q28364095-56A4007C-ABB0-4FE0-9D9B-BC8D4EFCCDC5Q28365699-BE079849-DF02-470A-996A-A4FE09A5A94EQ28367183-B5F5A5D6-9714-4FE7-9EFD-FD3A65886BA8Q28394719-6E12FFF9-BC6B-4575-A9CA-F749923D3280Q28509937-C3D344FC-9AE7-402F-AF67-1FB7537005F6Q28566471-5603F1F4-0586-4EF2-9698-754C1C0EAD31Q28572892-6161754E-DFB4-4C5F-8760-2B97A499EBEEQ29620204-5C2E0DD5-1EB5-43F6-9651-21281C282706Q30440963-9358472E-78FE-447E-AF18-F4CF9653A853Q30477065-8CBA4C45-FF5C-476E-A9D7-E446C04D3290Q30500139-4714DE6E-101D-4370-AA66-A943FDAFEA21Q32041819-7AD99BC6-D650-42DE-883E-24C702700DF1Q32081444-7B644929-ACD0-453C-8E66-1C35CA5009E3Q33338156-ED0DE73A-F887-4B67-B174-683F23D2AAD6Q33385837-99F5662B-10E1-40ED-A033-86642DA17D99Q33463351-DE39444A-99BD-4676-BE39-1049897E6675Q33627567-DAE9CDE4-8F11-4E1F-BC6C-5371B75126EAQ33637196-89B5CFDE-0D9D-4FB9-B668-2F24E7F09E55Q33757276-C3DDF389-7F1C-4F73-8627-1321E9ABF587Q33767581-FA6B1A27-AFB6-41B2-B183-CAD19D8DCF22
P2860
Cholesterol is required for surface transport of influenza virus hemagglutinin.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Cholesterol is required for surface transport of influenza virus hemagglutinin.
@en
type
label
Cholesterol is required for surface transport of influenza virus hemagglutinin.
@en
prefLabel
Cholesterol is required for surface transport of influenza virus hemagglutinin.
@en
P2860
P356
P1476
Cholesterol is required for surface transport of influenza virus hemagglutinin.
@en
P2093
P2860
P304
P356
10.1083/JCB.140.6.1357
P407
P50
P577
1998-03-01T00:00:00Z