Literature DB >> 10837758

Lipid vesicles and membrane fusion.

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Abstract

Membrane fusion is essential for cell survival and has attracted a great deal of both theoretical and experimental interest. Fluorescence (de)quenching measurements were designed to distinguish between bilayermerging and vesicle-mixing. Theoretical studies and various microscopic and diffraction methods have elucidated the mechanism of membrane fusion. These have revealed that membrane proximity and high defect density in the adjacent bilayers are the only prerequisites for fusion. Intermediates, such as stalk or inverse micellar structures can, but need not, be involved in vesicle fusion. Nonlamellar phase creation is accompanied by massive membrane fusion although it is not a requirement for bilayer merging. Propensity for membrane fusion is increased by increasing the local membrane disorder as well by performing manipulations that bring bilayers closer together. Membrane rigidification and enlarged bilayer separation opposes this trend. Membrane fusion is promoted by defects created in the bilayer due to the vicinity of lipid phase transition, lateral phase separation or domain generation, high local membrane curvature, osmotic or electric stress in or on the membrane; the addition of amphiphats or macromolecules which insert themselves into the membrane, freezing or other mechanical membrane perturbation have similar effects. Lowering the water activity by the addition of water soluble polymers or by partial system dehydration invokes membrane aggregation and hence facilitates fusion; as does the membrane charge neutralization after proton or other ion binding to the lipids and intermembrane scaffolding by proteins or other macromolecules. The alignment of defect rich domains and polypeptides or protein binding is pluripotent: not only does it increase the number of proximal defects in the bilayers, it triggers the vesicle aggregation and is fusogenic. Exceptions are the bound molecules that create steric or electrical barriers between the membranes which prevent fusion. Membrane fusion can be non-leaky but it is very common to lose material from the vesicle interior during the later stages of membrane unification, that is, after a few hundred microseconds following the induction of fusion.

Entities:  

Year:  1999        PMID: 10837758     DOI: 10.1016/s0169-409x(99)00030-7

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  46 in total

1.  A theoretical analysis of low-frequency sonophoresis: dependence of transdermal transport pathways on frequency and energy density.

Authors:  Ahmet Tezel; Ashley Sens; Samir Mitragotri
Journal:  Pharm Res       Date:  2002-12       Impact factor: 4.200

2.  Hydration-driven transport of deformable lipid vesicles through fine pores and the skin barrier.

Authors:  Gregor Cevc; Dieter Gebauer
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

3.  Field theoretic study of bilayer membrane fusion: II. Mechanism of a stalk-hole complex.

Authors:  K Katsov; M Müller; M Schick
Journal:  Biophys J       Date:  2005-11-04       Impact factor: 4.033

4.  Reverse hexagonal phase nanodispersion of monoolein and oleic acid for topical delivery of peptides: in vitro and in vivo skin penetration of cyclosporin A.

Authors:  Luciana B Lopes; Denise A Ferreira; Daniel de Paula; M Tereza J Garcia; José A Thomazini; Márcia C A Fantini; M Vitória L B Bentley
Journal:  Pharm Res       Date:  2006-05-25       Impact factor: 4.200

5.  A new mechanism of model membrane fusion determined from Monte Carlo simulation.

Authors:  M Müller; K Katsov; M Schick
Journal:  Biophys J       Date:  2003-09       Impact factor: 4.033

6.  Domain formation in DODAB-cholesterol mixed systems monitored via Nile Red anisotropy.

Authors:  Graham Hungerford; Elisabete M S Castanheira; Adelina L F Baptista; Paulo J G Coutinho; M Elisabete C D Real Oliveira
Journal:  J Fluoresc       Date:  2005-11       Impact factor: 2.217

7.  A simple method for the reconstitution of membrane proteins into giant unilamellar vesicles.

Authors:  Armelle Varnier; Frédérique Kermarrec; Iulia Blesneac; Christophe Moreau; Lavinia Liguori; Jean Luc Lenormand; Nathalie Picollet-D'hahan
Journal:  J Membr Biol       Date:  2010-02-05       Impact factor: 1.843

8.  Helical conformation of the SEVI precursor peptide PAP248-286, a dramatic enhancer of HIV infectivity, promotes lipid aggregation and fusion.

Authors:  Jeffrey R Brender; Kevin Hartman; Lindsey M Gottler; Marchello E Cavitt; Daniel W Youngstrom; Ayyalusamy Ramamoorthy
Journal:  Biophys J       Date:  2009-11-04       Impact factor: 4.033

9.  Membrane phase transition during heating and cooling: molecular insight into reversible melting.

Authors:  Liping Sun; Rainer A Böckmann
Journal:  Eur Biophys J       Date:  2017-07-19       Impact factor: 1.733

Review 10.  Hydrogen bonding interactions of liposomes simulating cell-cell recognition. A review.

Authors:  Constantinos M Paleos; Dimitris Tsiourvas; Zili Sideratou
Journal:  Orig Life Evol Biosph       Date:  2004-02       Impact factor: 1.950

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