Literature DB >> 7806567

Restricted movement of lipid and aqueous dyes through pores formed by influenza hemagglutinin during cell fusion.

J Zimmerberg1, R Blumenthal, D P Sarkar, M Curran, S J Morris.   

Abstract

The fusion of cells by influenza hemagglutinin (HA) is the best characterized example of protein-mediated membrane fusion. In simultaneous measurements of pairs of assays for fusion, we determined the order of detectable events during fusion. Fusion pore formation in HA-triggered cell-cell fusion was first detected by changes in cell membrane capacitance, next by a flux of fluorescent lipid, and finally by flux of aqueous fluorescent dye. Fusion pore conductance increased by small steps. A retardation of lipid and aqueous dyes occurred during fusion pore fluctuations. The flux of aqueous dye depended on the size of the molecule. The lack of movement of aqueous dyes while total fusion pore conductance increased suggests that initial HA-triggered fusion events are characterized by the opening of multiple small pores: the formation of a "sieve".

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Year:  1994        PMID: 7806567      PMCID: PMC2120276          DOI: 10.1083/jcb.127.6.1885

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  39 in total

1.  Observation of single influenza virus-cell fusion and measurement by fluorescence video microscopy.

Authors:  R J Lowy; D P Sarkar; Y Chen; R Blumenthal
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

2.  Patch clamp studies of single cell-fusion events mediated by a viral fusion protein.

Authors:  A E Spruce; A Iwata; J M White; W Almers
Journal:  Nature       Date:  1989-11-30       Impact factor: 49.962

3.  Real-time multi-wavelength fluorescence imaging of living cells.

Authors:  S J Morris
Journal:  Biotechniques       Date:  1990-03       Impact factor: 1.993

4.  Kinetics of pH-dependent fusion between 3T3 fibroblasts expressing influenza hemagglutinin and red blood cells. Measurement by dequenching of fluorescence.

Authors:  S J Morris; D P Sarkar; J M White; R Blumenthal
Journal:  J Biol Chem       Date:  1989-03-05       Impact factor: 5.157

5.  Currents through the fusion pore that forms during exocytosis of a secretory vesicle.

Authors:  L J Breckenridge; W Almers
Journal:  Nature       Date:  1987 Aug 27-Sep 2       Impact factor: 49.962

6.  Simultaneous electrical and optical measurements show that membrane fusion precedes secretory granule swelling during exocytosis of beige mouse mast cells.

Authors:  J Zimmerberg; M Curran; F S Cohen; M Brodwick
Journal:  Proc Natl Acad Sci U S A       Date:  1987-03       Impact factor: 11.205

Review 7.  The structure and function of the hemagglutinin membrane glycoprotein of influenza virus.

Authors:  D C Wiley; J J Skehel
Journal:  Annu Rev Biochem       Date:  1987       Impact factor: 23.643

8.  Capacitance measurements reveal stepwise fusion events in degranulating mast cells.

Authors:  J M Fernandez; E Neher; B D Gomperts
Journal:  Nature       Date:  1984 Nov 29-Dec 5       Impact factor: 49.962

9.  An efficient method for introducing macromolecules into living cells.

Authors:  S J Doxsey; J Sambrook; A Helenius; J White
Journal:  J Cell Biol       Date:  1985-07       Impact factor: 10.539

10.  Initial stages of influenza hemagglutinin-induced cell fusion monitored simultaneously by two fluorescent events: cytoplasmic continuity and lipid mixing.

Authors:  D P Sarkar; S J Morris; O Eidelman; J Zimmerberg; R Blumenthal
Journal:  J Cell Biol       Date:  1989-07       Impact factor: 10.539

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  78 in total

1.  Hemifusion between cells expressing hemagglutinin of influenza virus and planar membranes can precede the formation of fusion pores that subsequently fully enlarge.

Authors:  V I Razinkov; G B Melikyan; F S Cohen
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

2.  A specific point mutant at position 1 of the influenza hemagglutinin fusion peptide displays a hemifusion phenotype.

Authors:  H Qiao; R T Armstrong; G B Melikyan; F S Cohen; J M White
Journal:  Mol Biol Cell       Date:  1999-08       Impact factor: 4.138

3.  Tension of membranes expressing the hemagglutinin of influenza virus inhibits fusion.

Authors:  R M Markosyan; G B Melikyan; F S Cohen
Journal:  Biophys J       Date:  1999-08       Impact factor: 4.033

4.  Minimal aggregate size and minimal fusion unit for the first fusion pore of influenza hemagglutinin-mediated membrane fusion.

Authors:  J Bentz
Journal:  Biophys J       Date:  2000-01       Impact factor: 4.033

5.  A point mutation in the transmembrane domain of the hemagglutinin of influenza virus stabilizes a hemifusion intermediate that can transit to fusion.

Authors:  G B Melikyan; R M Markosyan; M G Roth; F S Cohen
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

6.  Reversible merger of membranes at the early stage of influenza hemagglutinin-mediated fusion.

Authors:  E Leikina; L V Chernomordik
Journal:  Mol Biol Cell       Date:  2000-07       Impact factor: 4.138

7.  Stochastic simulation of hemagglutinin-mediated fusion pore formation.

Authors:  S Schreiber; K Ludwig; A Herrmann; H G Holzhütter
Journal:  Biophys J       Date:  2001-09       Impact factor: 4.033

8.  Amino acid sequence requirements of the transmembrane and cytoplasmic domains of influenza virus hemagglutinin for viable membrane fusion.

Authors:  G B Melikyan; S Lin; M G Roth; F S Cohen
Journal:  Mol Biol Cell       Date:  1999-06       Impact factor: 4.138

9.  Membrane fusion mediated by coiled coils: a hypothesis.

Authors:  J Bentz
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

10.  Bilayers merge even when exocytosis is transient.

Authors:  Justin W Taraska; Wolfhard Almers
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-01       Impact factor: 11.205

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