Literature DB >> 2466492

Role of channels in the fusion of vesicles with a planar bilayer.

D J Woodbury1, J E Hall.   

Abstract

Fluorescence microscopy combined with electrical conductance measurements were used to assess fusion of phospholipid vesicles with a planar bilayer. Large unilamellar vesicles (0.5-3 microns diam.) filled with the fluorescent dye, calcein, were made both with or without porin channels. Vesicle-bilayer fusion was induced by increasing the osmolarity of the solution on the side of the bilayer to which the vesicles were added. Fusion was detected optically by the fluorescent flash due to release of vesicular contents. Although both porin-containing and porin-free vesicles give the same kind of flash upon content release, the conditions necessary to induce release are very different. Only 4% of the porin-free vesicles fuse (release their contents) when subjected to 3 M urea. However, the same conditions induce 53% of the porin-containing vesicles to fuse and most of these fusions occur at a lower osmolarity ([urea] less than 400 mM). Thus channels greatly enhance fusion in this model system. A physical model based on the postulate that fusion is induced by an increase in surface tension, predicts that three conditions are necessary for fusion in this system: (a) an open channel in the vesicle membrane, (b) an osmotic gradient across the bilayer, and (c) the vesicle in contact with the planar membrane. These are the conditions that experimentally produce fusion in the model system.

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Year:  1988        PMID: 2466492      PMCID: PMC1330417          DOI: 10.1016/S0006-3495(88)83042-X

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  21 in total

1.  Ca++-induced fusion of proteoliposomes: dependence on transmembrane osmotic gradient.

Authors:  C Miller; P Arvan; J N Telford; E Racker
Journal:  J Membr Biol       Date:  1976       Impact factor: 1.843

2.  Vesicle-membrane fusion. Observation of simultaneous membrane incorporation and content release.

Authors:  D J Woodbury; J E Hall
Journal:  Biophys J       Date:  1988-08       Impact factor: 4.033

3.  Formation of large, ion-permeable membrane channels by the matrix protein (porin) of Escherichia coli.

Authors:  R Benz; K Janko; W Boos; P Läuger
Journal:  Biochim Biophys Acta       Date:  1978-08-17

4.  The planar organization of lecithin-cholesterol bilayers.

Authors:  D M Engelman; J E Rothman
Journal:  J Biol Chem       Date:  1972-06-10       Impact factor: 5.157

5.  The water permeability of artificial bimolecular leaflets: a comparison of radio-tracer and osmotic methods.

Authors:  T Hanai; D A Haydon; W R Redwood
Journal:  Ann N Y Acad Sci       Date:  1966-07-14       Impact factor: 5.691

6.  Thermoelasticity of large lecithin bilayer vesicles.

Authors:  R Kwok; E Evans
Journal:  Biophys J       Date:  1981-09       Impact factor: 4.033

7.  Preparation of cell-size unilamellar liposomes with high captured volume and defined size distribution.

Authors:  S Kim; G M Martin
Journal:  Biochim Biophys Acta       Date:  1981-08-06

8.  Fusion of liposomes containing conductance probes with black lipid films.

Authors:  M R Moore
Journal:  Biochim Biophys Acta       Date:  1976-04-05

9.  A fluorescence assay to monitor vesicle fusion and lysis.

Authors:  D A Kendall; R C MacDonald
Journal:  J Biol Chem       Date:  1982-12-10       Impact factor: 5.157

10.  Fusion of phospholipid vesicles with planar phospholipid bilayer membranes. II. Incorporation of a vesicular membrane marker into the planar membrane.

Authors:  F S Cohen; J Zimmerberg; A Finkelstein
Journal:  J Gen Physiol       Date:  1980-03       Impact factor: 4.086

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  29 in total

1.  Ca(2+)-regulated, neurosecretory granule channel involved in release from neurohypophysial terminals.

Authors:  Yong Yin; Govindan Dayanithi; José R Lemos
Journal:  J Physiol       Date:  2002-03-01       Impact factor: 5.182

2.  Activation and conductance properties of ryanodine-sensitive calcium channels from brain microsomal membranes incorporated into planar lipid bilayers.

Authors:  R H Ashley
Journal:  J Membr Biol       Date:  1989-10       Impact factor: 1.843

3.  The chloroplast protein import channel Toc75: pore properties and interaction with transit peptides.

Authors:  Silke C Hinnah; Richard Wagner; Natalia Sveshnikova; Roswitha Harrer; Jürgen Soll
Journal:  Biophys J       Date:  2002-08       Impact factor: 4.033

4.  Computer detection of the rapid diffusion of fluorescent membrane fusion markers in images observed with video microscopy.

Authors:  W D Niles; Q Li; F S Cohen
Journal:  Biophys J       Date:  1992-09       Impact factor: 4.033

5.  Tension in secretory granule membranes causes extensive membrane transfer through the exocytotic fusion pore.

Authors:  J R Monck; G Alvarez de Toledo; J M Fernandez
Journal:  Proc Natl Acad Sci U S A       Date:  1990-10       Impact factor: 11.205

6.  The role of cavitation in liposome formation.

Authors:  Eric S Richardson; William G Pitt; Dixon J Woodbury
Journal:  Biophys J       Date:  2007-08-31       Impact factor: 4.033

7.  Making synaptic vesicles fuse with lipid bilayers.

Authors:  D J Woodbury
Journal:  Biophys J       Date:  1993-08       Impact factor: 4.033

8.  Reconstitution of a chloroplast protein import channel.

Authors:  S C Hinnah; K Hill; R Wagner; T Schlicher; J Soll
Journal:  EMBO J       Date:  1997-12-15       Impact factor: 11.598

9.  Flickering fusion pores comparable with initial exocytotic pores occur in protein-free phospholipid bilayers.

Authors:  A Chanturiya; L V Chernomordik; J Zimmerberg
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-23       Impact factor: 11.205

10.  Controlled delivery of proteins into bilayer lipid membranes on chip.

Authors:  Michele Zagnoni; Mairi E Sandison; Phedra Marius; Anthony G Lee; Hywel Morgan
Journal:  Lab Chip       Date:  2007-06-27       Impact factor: 6.799

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