Literature DB >> 3041004

Difference in capacities for virion-to-virion fusion of young and aged HVJ (Sendai virus): a model of membrane fusion.

J Kim, Y Okada.   

Abstract

Young and aged HVJ virions differ structurally and morphologically due to changes that occur during aging in vitro or in ovo. Young virions soon after their budding off are rod-shaped, rigid and relatively uniform in size, whereas virions that have aged in vitro after their formation are round, nonrigid and variable in size. These changes during aging seem to be due to the variation of M protein, a "skeletal" protein that is associated with both the envelope membrane proteins and nucleocapsid strands in the virions. The capacities for virion-to-virion fusion of young and aged virions were compared to clarify the relation between the membrane fusion and membrane-associating skeletal proteins. On treatment with polyethylene glycol (PEG), aged virions readily fused, forming large virion vesicles, but young virions were resistant to fusion. Further, aged virions fused even on incubation at 37 degrees C without the fusogen. Thus the capacity for virion-to-virion fusion evidently increases during aging of virions. This result suggests that skeletal proteins associating with the biological membrane are important for preventing membrane fusion, and that virion-to-virion fusion is a good model system for use in studies on the mechanism of membrane fusion.

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Year:  1987        PMID: 3041004     DOI: 10.1007/BF01869226

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  13 in total

1.  The structure of HVJ. II. The fine structure of the subunits.

Authors:  Y HOSAKA; Y NISHI; K FUKAI
Journal:  Biken J       Date:  1961-12

2.  Transformation of intramembrane particles of HVJ (Sendai virus) envelopes from an invisible to visible form on aging of virions.

Authors:  J Kim; K Hama; Y Miyake; Y Okada
Journal:  Virology       Date:  1979-06       Impact factor: 3.616

3.  Studies on the role of M protein in virus assembly using a ts mutant of HVJ (Sendai virus).

Authors:  T Yoshida; Y Nagai; K Maeno; M Iinuma; M Hamaguchi; T Matsumoto; S Nagayoshi; M Hoshino
Journal:  Virology       Date:  1979-01-15       Impact factor: 3.616

4.  Membrane (M) protein of HVJ (Sendai virus): its role in virus assembly.

Authors:  T Yoshida; S Nagai Y'Yoshii; K Maeno; T Matsumoto
Journal:  Virology       Date:  1976-05       Impact factor: 3.616

5.  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

6.  Trypsin action on the growth of Sendai virus in tissue culture cells. 3. Structural difference of Sendai viruses grown in eggs and tissue culture cells.

Authors:  M Homma; M Ouchi
Journal:  J Virol       Date:  1973-12       Impact factor: 5.103

7.  Parainfluenza virus surface projections: glycoproteins with haemagglutinin and neuraminidase activities.

Authors:  C Chen; R W Compans; P W Choppin
Journal:  J Gen Virol       Date:  1971-04       Impact factor: 3.891

8.  Proteins and glycoproteins of paramyxoviruses: a comparison of simian virus 5, Newcastle disease virus, and Sendai virus.

Authors:  W E Mountcastle; R W Compans; P W Choppin
Journal:  J Virol       Date:  1971-01       Impact factor: 5.103

9.  Intramembrane structural differentiation in Sendai virus maturation.

Authors:  T Bächi
Journal:  Virology       Date:  1980-10-15       Impact factor: 3.616

10.  Membrane alterations and other morphological features associated with polyethylene glycol-induced cell fusion.

Authors:  J M Robinson; D S Roos; R L Davidson; M J Karnovsky
Journal:  J Cell Sci       Date:  1979-12       Impact factor: 5.285

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  2 in total

1.  Human adipose tissue-derived stem cells exhibit proliferation potential and spontaneous rhythmic contraction after fusion with neonatal rat cardiomyocytes.

Authors:  Roxana Metzele; Christopher Alt; Xiaowen Bai; Yasheng Yan; Zhi Zhang; Zhizhong Pan; Michael Coleman; Jody Vykoukal; Yao-Hua Song; Eckhard Alt
Journal:  FASEB J       Date:  2010-11-08       Impact factor: 5.191

2.  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

  2 in total

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