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The mechanism of lamellar-to-inverted hexagonal phase transitions in phosphatidylethanolamine: implications for membrane fusion mechanisms

diterbitkan dalam: Biophysical Journal

tanggal publikasi: 1997-12-01

bahasa: Inggris

Cites articles 64

Date

Judul

Pengarang

1997-01-01

An early stage of membrane fusion mediated by the low pH conformation of influenza hemagglutinin depends upon membrane lipids
1997-06-01

Structural study of the relationship between the rate of membrane fusion and the ability of the fusion peptide of influenza virus to perturb bilayers

Richard M. Epand
1997-06-01

Nonlamellar phases induced by the interaction of gramicidin S with lipid bilayers. A possible relationship to membrane-disrupting activity.

Keir C. Neuman
1996-11-01

Mechanism of alamethicin insertion into lipid bilayers
1996-01-01

Small concentrations of alamethicin induce a cubic phase in bulk phosphatidylethanolamine mixtures

Sarah L. Keller
1996-01-01

Induction of nonbilayer structures in diacylphosphatidylcholine model membranes by transmembrane alpha-helical peptides: importance of hydrophobic mismatch and proposed role of tryptophans
1996-01-01

Structural study of the interaction between the SIV fusion peptide and model membranes

Richard M. Epand
1995-08-01

Bending membranes to the task: structural intermediates in bilayer fusion
1995-09-01

The hemifusion intermediate and its conversion to complete fusion: regulation by membrane composition
1995-07-01

Topological properties of two cubic phases of a phospholipid:cholesterol:diacylglycerol aqueous system and their possible implications in the phospholipase C-induced liposome fusion
1995-11-01

GPI-anchored influenza hemagglutinin induces hemifusion to both red blood cell and planar bilayer membranes
1995-07-01

Lipids in biological membrane fusion
1994-01-01

Phases and phase transitions of the hydrated phosphatidylethanolamines
1994-02-01

The mechanism of lamellar-to-inverted hexagonal phase transitions: a study using temperature-jump cryo-electron microscopy
1994-02-01

Inhibition of membrane fusion by lysophosphatidylcholine
1994-10-01

Bending, hydration and interstitial energies quantitatively account for the hexagonal-lamellar-hexagonal reentrant phase transition in dioleoylphosphatidylethanolamine
1993-03-01

Cryo-crinkling: what happens to carbon films on copper grids at low temperature
1993-11-01

Energetics of intermediates in membrane fusion: comparison of stalk and inverted micellar intermediate mechanisms
1993-12-01

Lysophosphatidylcholine reversibly arrests exocytosis and viral fusion at a stage between triggering and membrane merger
1993-04-01

Tension-stabilized pores in giant vesicles: determination of pore size and pore line tension.
1993-02-01

Lysolipids reversibly inhibit Ca(2+)-, GTP- and pH-dependent fusion of biological membranes.

Steven S. Vogel
1993-10-01

Structural requirements for the inhibition of membrane fusion by carbobenzoxy-D-Phe-Phe-Gly

Philip Yeagle, Richard M. Epand
1992-02-01

Kinetics of the lamellar-inverse hexagonal phase transition determined by time-resolved x-ray diffraction
1992-01-01

Photoinduced destabilization of liposomes
1992-10-01

The exocytotic fusion pore modeled as a lipidic pore
1992-10

1,2-Dioleoylglycerol promotes calcium-induced fusion in phospholipid vesicles

José Villalaín, Carmen San Martín, Juan C. Gómez-Fernández
1992-01-01

Hydrophobic lipid additives affect membrane stability and phase behavior of N-monomethyldioleoylphosphatidylethanolamine

Richard M. Epand
1991-03-01

Phospholipid phase transitions: kinetics and structural mechanisms

Manfred Kriechbaum
1991-02-01

Lipid polymorphism as observed by cryo-electron microscopy
1991-05-01

Effects of the 'fusion peptide' from measles virus on the structure of N-methyl dioleoylphosphatidylethanolamine membranes and their fusion with Sendai virus

Richard M. Epand
1990-07-01

Kinetics of the lamellar and hexagonal phase transitions in phosphatidylethanolamine. Time-resolved x-ray diffraction study using a microwave-induced temperature jump.
1990-01-01

Time-resolved cryotransmission electron microscopy

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