Published in Biophys J on May 01, 2000
Membrane fusion: stalk model revisited. Biophys J (2002) 2.83
The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement. J Membr Biol (2004) 2.59
Multiple roles for the actin cytoskeleton during regulated exocytosis. Cell Mol Life Sci (2012) 1.35
Time-resolved imaging of HIV-1 Env-mediated lipid and content mixing between a single virion and cell membrane. Mol Biol Cell (2005) 1.32
Osmotic and curvature stress affect PEG-induced fusion of lipid vesicles but not mixing of their lipids. Biophys J (2002) 1.21
Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion. J Cell Biol (2005) 1.19
Artificial cells: unique insights into exocytosis using liposomes and lipid nanotubes. Proc Natl Acad Sci U S A (2003) 1.15
SNARE complex zipping as a driving force in the dilation of proteinaceous fusion pores. J Membr Biol (2010) 1.11
Correlation between vesicle quantal size and fusion pore release in chromaffin cell exocytosis. Biophys J (2005) 1.08
Minimum membrane bending energies of fusion pores. J Membr Biol (2009) 1.00
Effects of membrane potential and sphingolipid structures on fusion of Semliki Forest virus. J Virol (2002) 0.97
Synaptotagmin IV modulation of vesicle size and fusion pores in PC12 cells. Biophys J (2010) 0.95
Temperature-dependent differences between readily releasable and reserve pool vesicles in chromaffin cells. Biochim Biophys Acta (2007) 0.92
Functional involvement of Annexin-2 in cAMP induced AQP2 trafficking. Pflugers Arch (2008) 0.90
Membrane tension and membrane fusion. Curr Opin Struct Biol (2015) 0.88
Initiation and dynamics of hemifusion in lipid bilayers. Biophys J (2003) 0.87
Linking differences in membrane tension with the requirement for a contractile actomyosin scaffold during exocytosis in salivary glands. Commun Integr Biol (2012) 0.83
Teardrop shapes minimize bending energy of fusion pores connecting planar bilayers. Phys Rev E Stat Nonlin Soft Matter Phys (2013) 0.82
Cdc42 controls the dilation of the exocytotic fusion pore by regulating membrane tension. Mol Biol Cell (2014) 0.81
Modeling excess retrieval in rat melanotroph membrane capacitance records. Biophys J (2002) 0.81
Molecular dynamics simulation analysis of membrane defects and pore propensity of hemifusion diaphragms. Biophys J (2013) 0.80
pH-Dependent Formation and Disintegration of the Influenza A Virus Protein Scaffold To Provide Tension for Membrane Fusion. J Virol (2015) 0.79
Hyperosmolarity reduces facilitation by a Ca(2+)-independent mechanism at the lobster neuromuscular junction: possible depletion of the releasable pool. J Physiol (2001) 0.78
Domain formation in membranes caused by lipid wetting of protein. Phys Rev E Stat Nonlin Soft Matter Phys (2008) 0.77
Increased catecholamine secretion from single adrenal chromaffin cells in DOCA-salt hypertension is associated with potassium channel dysfunction. ACS Chem Neurosci (2013) 0.76
Cholesterol Alters the Dynamics of Release in Protein Independent Cell Models for Exocytosis. Sci Rep (2016) 0.75
Dilation of fusion pores by crowding of SNARE proteins. Elife (2017) 0.75
Elastic properties of lipid bilayers: theory and possible experiments. Z Naturforsch C (1974) 19.89
Virus-cell and cell-cell fusion. Annu Rev Cell Dev Biol (1996) 5.83
Golgi tubule traffic and the effects of brefeldin A visualized in living cells. J Cell Biol (1997) 3.91
Energetics of intermediates in membrane fusion: comparison of stalk and inverted micellar intermediate mechanisms. Biophys J (1993) 3.82
Deformation and flow of membrane into tethers extracted from neuronal growth cones. Biophys J (1996) 3.42
Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells. Proc Natl Acad Sci U S A (1987) 3.37
Structural basis for membrane fusion by enveloped viruses. Mol Membr Biol (1999) 3.26
Final steps in exocytosis observed in a cell with giant secretory granules. Proc Natl Acad Sci U S A (1987) 3.01
Biomembrane fusion: a new concept derived from model studies using two interacting planar lipid bilayers. Biochim Biophys Acta (1987) 2.91
Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. II. Incorporation of a vesicular membrane marker into the planar membrane. J Gen Physiol (1980) 2.86
The hemifusion intermediate and its conversion to complete fusion: regulation by membrane composition. Biophys J (1995) 2.55
Measured effects of diacylglycerol on structural and elastic properties of phospholipid membranes. Biophys J (1996) 2.50
Physical measurements of bilayer-skeletal separation forces. Ann Biomed Eng (1995) 2.30
Flickering fusion pores comparable with initial exocytotic pores occur in protein-free phospholipid bilayers. Proc Natl Acad Sci U S A (1997) 2.25
On the theory of membrane fusion. The stalk mechanism. Gen Physiol Biophys (1984) 2.22
The exocytotic fusion pore modeled as a lipidic pore. Biophys J (1992) 1.99
Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. I. Discharge of vesicular contents across the planar membrane. J Gen Physiol (1980) 1.97
Tension in secretory granule membranes causes extensive membrane transfer through the exocytotic fusion pore. Proc Natl Acad Sci U S A (1990) 1.95
Video fluorescence microscopy studies of phospholipid vesicle fusion with a planar phospholipid membrane. Nature of membrane-membrane interactions and detection of release of contents. J Gen Physiol (1987) 1.71
Parameters affecting the fusion of unilamellar phospholipid vesicles with planar bilayer membranes. J Cell Biol (1984) 1.71
Lectins as chaperones in glycoprotein folding. Curr Opin Struct Biol (1998) 1.71
Exocytotic fusion pores exhibit semi-stable states. J Membr Biol (1993) 1.62
Regulation of exocytotic fusion by cell inflation. Biophys J (1998) 1.59
Regulation of endocytosis, exocytosis, and shape by membrane tension. Cold Spring Harb Symp Quant Biol (1995) 1.50
Is swelling of the secretory granule matrix the force that dilates the exocytotic fusion pore? Biophys J (1991) 1.40
The fusion kinetics of influenza hemagglutinin expressing cells to planar bilayer membranes is affected by HA density and host cell surface. J Gen Physiol (1995) 1.36
Effects of spontaneous bilayer curvature on influenza virus-mediated fusion pores. J Gen Physiol (1998) 1.36
Membrane mechanics can account for fusion pore dilation in stages. Biophys J (1995) 1.33
The role of the cytoplasmic tail region of influenza virus hemagglutinin in formation and growth of fusion pores. Virology (1997) 1.31
Ionic control of the size of the vesicle matrix of beige mouse mast cells. J Gen Physiol (1991) 1.29
Accelerated interleaflet transport of phosphatidylcholine molecules in membranes under deformation. Biophys J (1996) 1.28
Tension of membranes expressing the hemagglutinin of influenza virus inhibits fusion. Biophys J (1999) 1.24
Kinetics of release of serotonin from isolated secretory granules. II. Ion exchange determines the diffusivity of serotonin. Biophys J (1997) 1.17
Lipid flow through fusion pores connecting membranes of different tensions. Biophys J (1999) 1.13
Atomic force microscopy study of the secretory granule lumen. Biophys J (1996) 1.07
Resonance energy transfer imaging of phospholipid vesicle interaction with a planar phospholipid membrane: undulations and attachment sites in the region of calcium-mediated membrane--membrane adhesion. J Gen Physiol (1996) 1.03
High molecular weight polymers block cortical granule exocytosis in sea urchin eggs at the level of granule matrix disassembly. J Cell Biol (1989) 0.99
Reconstituting channels into planar membranes: a conceptual framework and methods for fusing vesicles to planar bilayer phospholipid membranes. Methods Enzymol (1993) 0.94
Evidence that the transition of HIV-1 gp41 into a six-helix bundle, not the bundle configuration, induces membrane fusion. J Cell Biol (2000) 5.71
The pathway of membrane fusion catalyzed by influenza hemagglutinin: restriction of lipids, hemifusion, and lipidic fusion pore formation. J Cell Biol (1998) 4.07
Membrane dipole potentials, hydration forces, and the ordering of water at membrane surfaces. Biophys J (1992) 3.98
Polymer inaccessible volume changes during opening and closing of a voltage-dependent ionic channel. Nature (1986) 3.89
Characterization of cholesterol-sphingomyelin domains and their dynamics in bilayer membranes. Biophys J (2001) 3.68
Lipids in biological membrane fusion. J Membr Biol (1995) 3.40
Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells. Proc Natl Acad Sci U S A (1987) 3.37
GPI-anchored influenza hemagglutinin induces hemifusion to both red blood cell and planar bilayer membranes. J Cell Biol (1995) 3.34
A voltage-dependent channel involved in nutrient uptake by red blood cells infected with the malaria parasite. Nature (2000) 3.14
A quantitative model for membrane fusion based on low-energy intermediates. Proc Natl Acad Sci U S A (2001) 3.01
Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. II. Incorporation of a vesicular membrane marker into the planar membrane. J Gen Physiol (1980) 2.86
An early stage of membrane fusion mediated by the low pH conformation of influenza hemagglutinin depends upon membrane lipids. J Cell Biol (1997) 2.73
Toxoplasma invasion: the parasitophorous vacuole is formed from host cell plasma membrane and pinches off via a fission pore. Proc Natl Acad Sci U S A (1996) 2.63
The hemifusion intermediate and its conversion to complete fusion: regulation by membrane composition. Biophys J (1995) 2.55
Inner but not outer membrane leaflets control the transition from glycosylphosphatidylinositol-anchored influenza hemagglutinin-induced hemifusion to full fusion. J Cell Biol (1997) 2.47
Osmotic swelling of phospholipid vesicles causes them to fuse with a planar phospholipid bilayer membrane. Science (1982) 2.43
Antimycin A mimics a cell-death-inducing Bcl-2 homology domain 3. Nat Cell Biol (2001) 2.43
Initial stages of influenza hemagglutinin-induced cell fusion monitored simultaneously by two fluorescent events: cytoplasmic continuity and lipid mixing. J Cell Biol (1989) 2.40
A specific point mutant at position 1 of the influenza hemagglutinin fusion peptide displays a hemifusion phenotype. Mol Biol Cell (1999) 2.34
Bax, but not Bcl-xL, decreases the lifetime of planar phospholipid bilayer membranes at subnanomolar concentrations. Proc Natl Acad Sci U S A (1999) 2.32
Infection of human tonsil histocultures: a model for HIV pathogenesis. Nat Med (1995) 2.31
Flickering fusion pores comparable with initial exocytotic pores occur in protein-free phospholipid bilayers. Proc Natl Acad Sci U S A (1997) 2.25
PB1-F2, an influenza A virus-encoded proapoptotic mitochondrial protein, creates variably sized pores in planar lipid membranes. J Virol (2004) 2.12
Lysolipids reversibly inhibit Ca(2+)-, GTP- and pH-dependent fusion of biological membranes. FEBS Lett (1993) 2.11
Amino acid sequence requirements of the transmembrane and cytoplasmic domains of influenza virus hemagglutinin for viable membrane fusion. Mol Biol Cell (1999) 2.10
Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. I. Discharge of vesicular contents across the planar membrane. J Gen Physiol (1980) 1.97
Osmotic swelling of vesicles: its role in the fusion of vesicles with planar phospholipid bilayer membranes and its possible role in exocytosis. Annu Rev Physiol (1986) 1.93
Structure-function of the channel-forming colicins. Annu Rev Biophys Biomol Struct (1995) 1.89
Electrical properties of skin at moderate voltages: contribution of appendageal macropores. Biophys J (1998) 1.87
The initial fusion pore induced by baculovirus GP64 is large and forms quickly. J Cell Biol (1996) 1.84
Experimental HIV infection of human lymphoid tissue: correlation of CD4+ T cell depletion and virus syncytium-inducing/non-syncytium-inducing phenotype in histocultures inoculated with laboratory strains and patient isolates of HIV type 1. AIDS Res Hum Retroviruses (1997) 1.72
Video fluorescence microscopy studies of phospholipid vesicle fusion with a planar phospholipid membrane. Nature of membrane-membrane interactions and detection of release of contents. J Gen Physiol (1987) 1.71
Parameters affecting the fusion of unilamellar phospholipid vesicles with planar bilayer membranes. J Cell Biol (1984) 1.71
Implications of lipid microdomains for membrane curvature, budding and fission. Curr Opin Cell Biol (2001) 1.67
Bending membranes to the task: structural intermediates in bilayer fusion. Curr Opin Struct Biol (1995) 1.62
Evidence for the HIV-1 phenotype switch as a causal factor in acquired immunodeficiency. Nat Med (1998) 1.62
Exocytotic fusion pores exhibit semi-stable states. J Membr Biol (1993) 1.62
Irreversible swelling of secretory granules during exocytosis caused by calcium. Nature (1985) 1.60
An amphipathic peptide from the C-terminal region of the human immunodeficiency virus envelope glycoprotein causes pore formation in membranes. J Virol (1994) 1.59
The lipid-anchored ectodomain of influenza virus hemagglutinin (GPI-HA) is capable of inducing nonenlarging fusion pores. Mol Biol Cell (2000) 1.59
Role of the cytoplasmic tail of ecotropic moloney murine leukemia virus Env protein in fusion pore formation. J Virol (2000) 1.56
Low pH is required for avian sarcoma and leukosis virus Env-induced hemifusion and fusion pore formation but not for pore growth. J Virol (2004) 1.52
Control of baculovirus gp64-induced syncytium formation by membrane lipid composition. J Virol (1995) 1.51
Multiple local contact sites are induced by GPI-linked influenza hemagglutinin during hemifusion and flickering pore formation. Traffic (2000) 1.50
Studies on the mechanism of action of channel-forming colicins using artificial membranes. J Membr Biol (1984) 1.45
Membrane permeability changes at early stages of influenza hemagglutinin-mediated fusion. Biophys J (2003) 1.43
Human immunodeficiency virus type 1 Env with an intersubunit disulfide bond engages coreceptors but requires bond reduction after engagement to induce fusion. J Virol (2003) 1.43
A point mutation in the transmembrane domain of the hemagglutinin of influenza virus stabilizes a hemifusion intermediate that can transit to fusion. Mol Biol Cell (2000) 1.43
Pro-apoptotic cleavage products of Bcl-xL form cytochrome c-conducting pores in pure lipid membranes. J Biol Chem (2001) 1.43
Synchronized activation and refolding of influenza hemagglutinin in multimeric fusion machines. J Cell Biol (2001) 1.42
Biochemical and functional studies of cortical vesicle fusion: the SNARE complex and Ca2+ sensitivity. J Cell Biol (1998) 1.42
The fusion kinetics of influenza hemagglutinin expressing cells to planar bilayer membranes is affected by HA density and host cell surface. J Gen Physiol (1995) 1.36
Effects of spontaneous bilayer curvature on influenza virus-mediated fusion pores. J Gen Physiol (1998) 1.36
"Entropic traps" in the kinetics of phase separation in multicomponent membranes stabilize nanodomains. Biophys J (2006) 1.34
The anti-influenza virus agent 4-GU-DANA (zanamivir) inhibits cell fusion mediated by human parainfluenza virus and influenza virus HA. J Virol (2000) 1.34
Membrane mechanics can account for fusion pore dilation in stages. Biophys J (1995) 1.33
Separation of the osmotically driven fusion event from vesicle-planar membrane attachment in a model system for exocytosis. J Cell Biol (1984) 1.33
Exocytosis of sea urchin egg cortical vesicles in vitro is retarded by hyperosmotic sucrose: kinetics of fusion monitored by quantitative light-scattering microscopy. J Cell Biol (1985) 1.32
Transanal hemorrhoidal dearterialization is an alternative to operative hemorrhoidectomy. Am J Surg (2001) 1.32
The role of the cytoplasmic tail region of influenza virus hemagglutinin in formation and growth of fusion pores. Virology (1997) 1.31
Influenza hemagglutinin-mediated fusion pores connecting cells to planar membranes: flickering to final expansion. J Gen Physiol (1993) 1.31
Acidic pH induces fusion of cells infected with baculovirus to form syncytia. FEBS Lett (1992) 1.26
A discrete stage of baculovirus GP64-mediated membrane fusion. Mol Biol Cell (1999) 1.25
Tension of membranes expressing the hemagglutinin of influenza virus inhibits fusion. Biophys J (1999) 1.24
Mechanism of electroinduced ionic species transport through a multilamellar lipid system. Biophys J (1995) 1.22
Comparison of transient and successful fusion pores connecting influenza hemagglutinin expressing cells to planar membranes. J Gen Physiol (1995) 1.21
An analysis of the role of the target membrane on the Gp64-induced fusion pore. Virology (1999) 1.21
A lipid/protein complex hypothesis for exocytotic fusion pore formation. Ann N Y Acad Sci (1991) 1.20
Single cell fusion events induced by influenza hemagglutinin: studies with rapid-flow, quantitative fluorescence microscopy. Exp Cell Res (1991) 1.20
Voltage-dependent translocation of R18 and DiI across lipid bilayers leads to fluorescence changes. Biophys J (1996) 1.19
Structure and dynamics of the colicin E1 channel. Mol Microbiol (1990) 1.19
Fusion pore conductance: experimental approaches and theoretical algorithms. Biophys J (1998) 1.19
Influenza virus hemagglutinin-induced cell-planar bilayer fusion: quantitative dissection of fusion pore kinetics into stages. J Gen Physiol (1993) 1.16
Sterols and sphingolipids strongly affect the growth of fusion pores induced by the hemagglutinin of influenza virus. Biochemistry (2000) 1.16
Structural intermediates in influenza haemagglutinin-mediated fusion. Mol Membr Biol (1999) 1.16
Hydrostatic pressures developed by osmotically swelling vesicles bound to planar membranes. J Gen Physiol (1989) 1.15
Calcium can disrupt the SNARE protein complex on sea urchin egg secretory vesicles without irreversibly blocking fusion. J Biol Chem (1998) 1.14
Micromolar Ca2+ stimulates fusion of lipid vesicles with planar bilayers containing a calcium-binding protein. Science (1980) 1.13
Lipid flow through fusion pores connecting membranes of different tensions. Biophys J (1999) 1.13
Membrane topography of ColE1 gene products: the hydrophobic anchor of the colicin E1 channel is a helical hairpin. J Bacteriol (1991) 1.11
Behavior of cells in rotating electric fields with account to surface charges and cell structures. Biophys J (1986) 1.09
Glutamine-enriched diets support muscle glutamine metabolism without stimulating tumor growth. J Surg Res (1990) 1.06
Poisson-distributed active fusion complexes underlie the control of the rate and extent of exocytosis by calcium. J Cell Biol (1996) 1.06
Completion of trimeric hairpin formation of influenza virus hemagglutinin promotes fusion pore opening and enlargement. Virology (2003) 1.06