Literature DB >> 1705483

Fusion of enveloped viruses with cells and liposomes. Activity and inactivation.

S Nir1, N Düzgünes, M C de Lima, D Hoekstra.   

Abstract

The fusion of viruses with cells and liposomes is reviewed with focus on the analysis of the final extents and kinetics of fusion. Influenza virus and Sendai virus exhibit 100% of fusion capacity with cells at pH 5 and pH 7.5, respectively. On the other hand, there may be in certain cases, a limit on the number of virions that can fuse with a single cell, that is significantly below the limit on binding. It still remains to be resolved whether this limit reflects a limited number of possible fusion sites, or a saturation limit on the amount of viral glycoproteins that can be incorporated in the cellular membrane, like the case of virus fusion with pure phospholipid vesicles, in which the fusion products were shown to consist of a single virus and several liposomes. Both viruses demonstrate incomplete fusion activity towards liposomes of a variety of compositions. In the case of Sendai virus, fusion inactive virions bind essentially irreversibly to liposomes. Yet, preliminary results revealed that such bound, unfused virions can be released by sucrose gradient centrifugation. The separated unfused virions subsequently fuse when incubated with a "fresh" batch of liposomes. We conclude, therefore, that the fraction of initially bound unfused virions does not consist of dective particles, but rather of particles bound to liposomes via "inactive" sites. Details of the low pH inactivation of fusion capacity of influenza virus towards cells and liposomes are presented. This inactivation is caused by protonation and exposure of the hydrophobic segment of HA2, and affects primarily the fusion rate constants. Some degree of inactivation also occurs when virions are bound to cellular membranes.

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Year:  1990        PMID: 1705483     DOI: 10.1007/bf02990496

Source DB:  PubMed          Journal:  Cell Biophys        ISSN: 0163-4992


  57 in total

1.  Sequence determination of the Sendai virus fusion protein gene.

Authors:  B M Blumberg; C Giorgi; K Rose; D Kolakofsky
Journal:  J Gen Virol       Date:  1985-02       Impact factor: 3.891

2.  Effect of synexin on aggregation and fusion of chromaffin granule ghosts at pH 6.

Authors:  S Nir; A Stutzin; H B Pollard
Journal:  Biochim Biophys Acta       Date:  1987-10-02

3.  Identification of biological activities of paramyxovirus glycoproteins. Activation of cell fusion, hemolysis, and infectivity of proteolytic cleavage of an inactive precursor protein of Sendai virus.

Authors:  A Scheid; P W Choppin
Journal:  Virology       Date:  1974-02       Impact factor: 3.616

4.  Effect of cholesterol on Ca2+-induced aggregation and fusion of sonicated phosphatidylserine/cholesterol vesicles.

Authors:  G Braun; P I Lelkes; S Nir
Journal:  Biochim Biophys Acta       Date:  1985-02-14

5.  Ca2+-induced fusion of large unilamellar phosphatidylserine/cholesterol vesicles.

Authors:  M Bental; J Wilschut; J Scholma; S Nir
Journal:  Biochim Biophys Acta       Date:  1987-04-09

6.  Sendai virus membrane fusion: time course and effect of temperature, pH, calcium, and receptor concentration.

Authors:  A M Haywood; B P Boyer
Journal:  Biochemistry       Date:  1982-11-23       Impact factor: 3.162

7.  Mechanism of fusion of Sendai virus: role of hydrophobic interactions and mobility constraints of viral membrane proteins. Effects of polyethylene glycol.

Authors:  D Hoekstra; K Klappe; H Hoff; S Nir
Journal:  J Biol Chem       Date:  1989-04-25       Impact factor: 5.157

8.  Pyrene phospholipid as a biological fluorescent probe for studying fusion of virus membrane with liposomes.

Authors:  R Pal; Y Barenholz; R R Wagner
Journal:  Biochemistry       Date:  1988-01-12       Impact factor: 3.162

9.  Role of synexin in membrane fusion. Enhancement of calcium-dependent fusion of phospholipid vesicles.

Authors:  K Hong; N Düzgüneş; D Papahadjopoulos
Journal:  J Biol Chem       Date:  1981-04-25       Impact factor: 5.157

10.  Electron microscopy of the low pH structure of influenza virus haemagglutinin.

Authors:  R W Ruigrok; N G Wrigley; L J Calder; S Cusack; S A Wharton; E B Brown; J J Skehel
Journal:  EMBO J       Date:  1986-01       Impact factor: 11.598

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  16 in total

1.  Kinetics of influenza virus fusion with the endosomal and plasma membranes of cultured cells. Effect of temperature.

Authors:  I Nunes-Correia; S Nir; M C Pedroso de Lima
Journal:  J Membr Biol       Date:  2003-09-01       Impact factor: 1.843

2.  Evidence that rabies virus forms different kinds of fusion machines with different pH thresholds for fusion.

Authors:  Stéphane Roche; Yves Gaudin
Journal:  J Virol       Date:  2004-08       Impact factor: 5.103

3.  Two distinct low-pH steps promote entry of vaccinia virus.

Authors:  Alan C Townsley; Bernard Moss
Journal:  J Virol       Date:  2007-06-06       Impact factor: 5.103

4.  Measuring pKa of activation and pKi of inactivation for influenza hemagglutinin from kinetics of membrane fusion of virions and of HA expressing cells.

Authors:  Aditya Mittal; Tong Shangguan; Joe Bentz
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

5.  Aggregation of hapten-bearing liposomes mediated by specific antibodies.

Authors:  K D Lee; A B Kantor; S Nir; J C Owicki
Journal:  Biophys J       Date:  1993-03       Impact factor: 4.033

6.  Analysis of delay times of hemagglutinin-mediated fusion between influenza virus and cell membranes.

Authors:  K Ludwig; T Korte; A Herrmann
Journal:  Eur Biophys J       Date:  1995       Impact factor: 1.733

7.  pH-dependent binding of the fluorophore bis-ANS to influenza virus reflects the conformational change of hemagglutinin.

Authors:  T Korte; A Herrmann
Journal:  Eur Biophys J       Date:  1994       Impact factor: 1.733

8.  Fusion between Newcastle disease virus and erythrocyte ghosts using octadecyl Rhodamine B fluorescence assay produces dequenching curves that fit the sum of two exponentials.

Authors:  C Cobaleda; A García-Sastre; E Villar
Journal:  Biochem J       Date:  1994-06-01       Impact factor: 3.857

9.  The Murray Valley encephalitis virus prM protein confers acid resistance to virus particles and alters the expression of epitopes within the R2 domain of E glycoprotein.

Authors:  F Guirakhoo; R A Bolin; J T Roehrig
Journal:  Virology       Date:  1992-12       Impact factor: 3.616

10.  Intermediates and kinetics of membrane fusion.

Authors:  J Bentz
Journal:  Biophys J       Date:  1992-08       Impact factor: 4.033

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