Membrane mechanics can account for fusion pore dilation in stages
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Cholesterol promotes hemifusion and pore widening in membrane fusion induced by influenza hemagglutinin.Effects of spontaneous bilayer curvature on influenza virus-mediated fusion pores.Fusion-pore expansion during syncytium formation is restricted by an actin networkDilation of fusion pores by crowding of SNARE proteinsMinimum membrane bending energies of fusion pores.Sphingomyelin metabolism controls the shape and function of the Golgi cisternae.Pressure is proinflammatory in lung venular capillaries.Membrane bending energy and fusion pore kinetics in Ca(2+)-triggered exocytosisIt's what's inside that mattersAre the curves in all the right places?Dynamics of fusion pores connecting membranes of different tensionsMembrane permeability changes at early stages of influenza hemagglutinin-mediated fusion.Artificial cells: unique insights into exocytosis using liposomes and lipid nanotubes.A continuum model of docking of synaptic vesicle to plasma membrane.Teardrop shapes minimize bending energy of fusion pores connecting planar bilayers.Elastic energy of polyhedral bilayer vesicles.Membranes of the world unite!Biochemical and functional studies of cortical vesicle fusion: the SNARE complex and Ca2+ sensitivity.The Nanomechanics of Lipid Multibilayer Stacks Exhibits Complex Dynamics.A comparison of coarse-grained and continuum models for membrane bending in lipid bilayer fusion pores.Calculating Transition Energy Barriers and Characterizing Activation States for Steps of FusionCholesterol Increases the Openness of SNARE-Mediated Flickering Fusion PoresInitial size and dynamics of viral fusion pores are a function of the fusion protein mediating membrane fusionIncreased catecholamine secretion from single adrenal chromaffin cells in DOCA-salt hypertension is associated with potassium channel dysfunction.Palmitoylation contributes to membrane curvature in Influenza A virus assembly and hemagglutinin-mediated membrane fusion.Fusion pores and their control of neurotransmitter and hormone release.Membrane fusion: stalk model revisited.The gaussian curvature elastic modulus of N-monomethylated dioleoylphosphatidylethanolamine: relevance to membrane fusion and lipid phase behavior.SNARE complex zipping as a driving force in the dilation of proteinaceous fusion pores.Adhesion energy can regulate vesicle fusion and stabilize partially fused states.v-SNARE transmembrane domains function as catalysts for vesicle fusionCurvature-driven pore growth in charged membranes during charge-pulse and voltage-clamp experiments.Asymmetric Phosphatidylethanolamine Distribution Controls Fusion Pore Lifetime and Probability.
P2860
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P2860
Membrane mechanics can account for fusion pore dilation in stages
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Membrane mechanics can account for fusion pore dilation in stages
@ast
Membrane mechanics can account for fusion pore dilation in stages
@en
Membrane mechanics can account for fusion pore dilation in stages
@nl
type
label
Membrane mechanics can account for fusion pore dilation in stages
@ast
Membrane mechanics can account for fusion pore dilation in stages
@en
Membrane mechanics can account for fusion pore dilation in stages
@nl
prefLabel
Membrane mechanics can account for fusion pore dilation in stages
@ast
Membrane mechanics can account for fusion pore dilation in stages
@en
Membrane mechanics can account for fusion pore dilation in stages
@nl
P2093
P2860
P1433
P1476
Membrane mechanics can account for fusion pore dilation in stages
@en
P2093
A Shcherbakov
J Zimmerberg
Y A Chizmadzhev
P2860
P304
P356
10.1016/S0006-3495(95)80119-0
P407
P577
1995-12-01T00:00:00Z