Literature DB >> 8636231

Membrane fusion mediated by the influenza virus hemagglutinin requires the concerted action of at least three hemagglutinin trimers.

T Danieli1, S L Pelletier, Y I Henis, J M White.   

Abstract

In this study we tested the hypothesis that fusion mediated by the influenza virus hemagglutinin (HA) is a cooperative event. To so this we characterized 3T3 cell lines that express HA at nine different defined surface densities. HA densities ranged from 1.0 to 12.6 x 10(3) HA trimers/microns2 as determined by quantitative fluorescent antibody binding. The lateral mobility and percent mobile fraction of HA did not vary significantly among these cells, nor did the contact area between HA-expressing cells and target RBCs. The fusion reaction of each HA-expressing cell line was analyzed using a fluorescence dequenching assay that uses octadecylrhodamine (R18)-labeled RBCs. For each cell line we measured the lag time preceding the onset of fusion, the initial rate of fusion, and final extent of fusion. The final extent of fusion was similar for all cell lines, and the initial rate of fusion as a function of HA surface density displayed a Michaelis-Menten-type dependence. However, the dependence of the lag time preceding the onset of fusion on HA surface density was clearly sigmoidal. Kinetic analysis of the data for the reciprocal lag time vs HA surface density, by both a log/log plot and a Hill plot, suggested that the observed sigmoidicity does not reflect cooperativity at the level of formation of HA aggregates as a prerequisite to fusion. Rather, the cooperativity of the process(es) that occur(s) during the lag time arises at a later step and involves a minimum of three, and most likely four, HA trimers. A model is proposed to explain HA cooperativity during fusion.

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Year:  1996        PMID: 8636231      PMCID: PMC2120819          DOI: 10.1083/jcb.133.3.559

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


  64 in total

1.  An architecture for the fusion site of influenza hemagglutinin.

Authors:  J Bentz; H Ellens; D Alford
Journal:  FEBS Lett       Date:  1990-12-10       Impact factor: 4.124

Review 2.  Protein-mediated membrane fusion.

Authors:  T Stegmann; R W Doms; A Helenius
Journal:  Annu Rev Biophys Biophys Chem       Date:  1989

3.  Phospholipid interactions of synthetic peptides representing the N-terminus of HIV gp41.

Authors:  M Rafalski; J D Lear; W F DeGrado
Journal:  Biochemistry       Date:  1990-08-28       Impact factor: 3.162

4.  Delay time for influenza virus hemagglutinin-induced membrane fusion depends on hemagglutinin surface density.

Authors:  M J Clague; C Schoch; R Blumenthal
Journal:  J Virol       Date:  1991-05       Impact factor: 5.103

5.  Conformational changes and fusion activity of influenza virus hemagglutinin of the H2 and H3 subtypes: effects of acid pretreatment.

Authors:  A Puri; F P Booy; R W Doms; J M White; R Blumenthal
Journal:  J Virol       Date:  1990-08       Impact factor: 5.103

6.  Orientation into the lipid bilayer of an asymmetric amphipathic helical peptide located at the N-terminus of viral fusion proteins.

Authors:  R Brasseur; M Vandenbranden; B Cornet; A Burny; J M Ruysschaert
Journal:  Biochim Biophys Acta       Date:  1990-11-16

7.  Fusion activity of influenza virus PR8/34 correlates with a temperature-induced conformational change within the hemagglutinin ectodomain detected by photochemical labeling.

Authors:  J Brunner; C Zugliani; R Mischler
Journal:  Biochemistry       Date:  1991-03-05       Impact factor: 3.162

8.  Fusion of influenza hemagglutinin-expressing fibroblasts with glycophorin-bearing liposomes: role of hemagglutinin surface density.

Authors:  H Ellens; J Bentz; D Mason; F Zhang; J M White
Journal:  Biochemistry       Date:  1990-10-16       Impact factor: 3.162

9.  Intermediates in influenza induced membrane fusion.

Authors:  T Stegmann; J M White; A Helenius
Journal:  EMBO J       Date:  1990-12       Impact factor: 11.598

10.  Lines of BPV-transformed murine cells that constitutively express influenza virus hemagglutinin.

Authors:  J Sambrook; L Rodgers; J White; M J Gething
Journal:  EMBO J       Date:  1985-01       Impact factor: 11.598

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  158 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.  Evolution of intermediates of influenza virus hemagglutinin-mediated fusion revealed by kinetic measurements of pore formation.

Authors:  R M Markosyan; G B Melikyan; F S Cohen
Journal:  Biophys J       Date:  2001-02       Impact factor: 4.033

3.  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

4.  Soluble receptor-induced retroviral infection of receptor-deficient cells.

Authors:  R Damico; P Bates
Journal:  J Virol       Date:  2000-07       Impact factor: 5.103

5.  Role of hemagglutinin surface density in the initial stages of influenza virus fusion: lack of evidence for cooperativity.

Authors:  S Günther-Ausborn; P Schoen; I Bartoldus; J Wilschut; T Stegmann
Journal:  J Virol       Date:  2000-03       Impact factor: 5.103

6.  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

7.  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

8.  Identification of a receptor-binding pocket on the envelope protein of friend murine leukemia virus.

Authors:  R A Davey; Y Zuo; J M Cunningham
Journal:  J Virol       Date:  1999-05       Impact factor: 5.103

9.  Crystal structure of human T cell leukemia virus type 1 gp21 ectodomain crystallized as a maltose-binding protein chimera reveals structural evolution of retroviral transmembrane proteins.

Authors:  B Kobe; R J Center; B E Kemp; P Poumbourios
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-13       Impact factor: 11.205

10.  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

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