Literature DB >> 6314100

Subcellular location of the major protein antigens of paramyxoviruses revealed by immunoperoxidase cytochemistry.

Y Nagai, T Yoshida, M Hamaguchi, H Nagura, H Hasegawa, S Yoshimura, K Watanabe.   

Abstract

The major structural proteins of Newcastle disease virus and Sendai virus were localized in infected BHK-21 and MDBK cells by ultrastructural immunoperoxidase cytochemistry using antibodies against the individual viral protein antigens. The intracellular glycoproteins were strictly membrane bound, being localized in the rough endoplasmic reticulum (RER), perinuclear spaces, smooth membrane vesicles, and presumed Golgi apparatus. The nucleocapsid proteins were detected exclusively in membrane free cytosol and accumulated there, forming inclusions. The membrane (M) protein was found both in cytosol and on RER. The viral proteins on RER exhibited a distinct site specificity; the glycoproteins were facing the lumen of RER whereas M protein was present at the outer cytoplasmic surface. All the viral proteins were detectable at the plasma membrane where virus assembly takes place. However, their modes of distribution differed remarkably. The glycoproteins were spread widely over the entire cell surface including the areas of virus budding and those of normal morphology, whereas M protein was localized in restricted areas of the membrane, frequently forming a patch of virus specific membrane. The presence of nucleocapsids was confined to the virus particles budding from the plasma membrane. These results complement and extend the earlier morphological and biochemical data on the assembly or morphogenesis of paramyxoviruses.

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Year:  1983        PMID: 6314100     DOI: 10.1111/j.1348-0421.1983.tb00614.x

Source DB:  PubMed          Journal:  Microbiol Immunol        ISSN: 0385-5600            Impact factor:   1.955


  7 in total

1.  A temperature-sensitive mutant of Newcastle disease virus defective in intracellular processing of fusion protein.

Authors:  H Matsumura; Y Futaesaku; S Kohno; A Sugiura; M Kohase
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

2.  Versatility of the accessory C proteins of Sendai virus: contribution to virus assembly as an additional role.

Authors:  M K Hasan; A Kato; M Muranaka; R Yamaguchi; Y Sakai; I Hatano; M Tashiro; Y Nagai
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

3.  The ultrastructural changes of S-100 protein localization during lipolysis in adipocytes. An immunoelectron-microscopic study.

Authors:  H Haimoto; K Kato; F Suzuki; H Nagura
Journal:  Am J Pathol       Date:  1985-11       Impact factor: 4.307

4.  Nucleotide sequence of a Sendai virus genome region covering the entire M gene and the 3' proximal 1013 nucleotides of the F gene.

Authors:  Y Hidaka; T Kanda; K Iwasaki; A Nomoto; T Shioda; H Shibuta
Journal:  Nucleic Acids Res       Date:  1984-11-12       Impact factor: 16.971

5.  Monoclonal antibodies against avian paramyxovirus-3: antigenic mapping and functional analysis of the haemagglutinin-neuraminidase protein and the characterization of nonspecific monoclonal antibodies.

Authors:  C L Anderson; P H Russell
Journal:  Arch Virol       Date:  1988       Impact factor: 2.574

Review 6.  Virological applications of the grid-cell-culture technique.

Authors:  A D Hyatt; B T Eaton
Journal:  Electron Microsc Rev       Date:  1990

7.  Inhibition of the assembly of Newcastle disease virus by monensin.

Authors:  T Yoshida; Y Nakayama; H Nagura; T Toyoda; K Nishikawa; M Hamaguchi; Y Nagai
Journal:  Virus Res       Date:  1986-02       Impact factor: 3.303

  7 in total

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