Literature DB >> 6204863

Monoclonal antibodies against simian virus 40 nuclear large T tumour antigen: epitope mapping, papova virus cross-reaction and cell surface staining.

R K Ball, B Siegl, S Quellhorst, G Brandner, D G Braun.   

Abstract

Thirty six cloned hybridomas have been isolated which produce monoclonal antibodies directed against simian virus 40 (SV40) large T tumour antigen. They have been shown to recognize at least six different epitopes along the T antigen polypeptide according to their reaction with the various truncated forms of T antigen expressed by adenovirus-SV 40 hybrid viruses. Sixteen antibodies cross-react with cells infected by the closely related human BK virus. Only two antibodies, PAb1604 and PAb1614, directed against different epitopes of the SV40 T antigen, cross-react with polyoma large T tumour antigen which has a more limited amino acid sequence homology. This cross-reaction is rarely seen with polyclonal antibodies. Monoclonal antibody PAb1620 gave nuclear immunofluorescence only with murine cells transformed by SV40 and was found to react with a complex of T-antigen and 53 000-dalton host-coded protein. All the monoclonal antibodies react with nuclear T antigen and all but four antibodies stained the surface of SV40-transformed cells. These were four of the five antibodies directed against the central third of the T antigen. Thus the monoclonal antibodies show that cell surface T antigen differs from nuclear T antigen, either in accessibility or structure.

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Year:  1984        PMID: 6204863      PMCID: PMC557548          DOI: 10.1002/j.1460-2075.1984.tb02000.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  45 in total

1.  The nucleotide sequence and genome organization of the polyoma early region: extensive nucleotide and amino acid homology with SV40.

Authors:  T Friedmann; A Esty; P LaPorte; P Deininger
Journal:  Cell       Date:  1979-07       Impact factor: 41.582

2.  Identification and partial characterization of new antigens from simian virus 40-transformed mouse cells.

Authors:  C Chang; D T Simmons; M A Martin; P T Mora
Journal:  J Virol       Date:  1979-08       Impact factor: 5.103

3.  Subcellular Localization of simian virus 40 large tumor antigen.

Authors:  H R Soule; J S Butel
Journal:  J Virol       Date:  1979-05       Impact factor: 5.103

4.  Isolation of simian virus 40 from a newborn child.

Authors:  G Brandner; A Burger; D Neumann-Haefelin; C Reinke; H Helwig
Journal:  J Clin Microbiol       Date:  1977-02       Impact factor: 5.948

5.  Growth of primary plasmacytomas in the mineral oil-conditioned peritoneal environment.

Authors:  M Potter; J G Pumphrey; J L Walters
Journal:  J Natl Cancer Inst       Date:  1972-07       Impact factor: 13.506

6.  Inhibition of SV40-induced cellular DNA synthesis by microinjection of monoclonal antibodies.

Authors:  W E Mercer; D Nelson; J K Hyland; C M Croce; R Baserga
Journal:  Virology       Date:  1983-05       Impact factor: 3.616

7.  A simple cytochemical technique for demonstration of DNA in cells infected with mycoplasmas and viruses.

Authors:  W C Russell; C Newman; D H Williamson
Journal:  Nature       Date:  1975-02-06       Impact factor: 49.962

8.  A better cell line for making hybridomas secreting specific antibodies.

Authors:  M Shulman; C D Wilde; G Köhler
Journal:  Nature       Date:  1978-11-16       Impact factor: 49.962

9.  Simian virus 40-transformed cells express new species of proteins precipitable by anti-simian virus 40 tumor serum.

Authors:  M Kress; E May; R Cassingena; P May
Journal:  J Virol       Date:  1979-08       Impact factor: 5.103

10.  Somatic cell hybrids producing antibodies specific for the tumor antigen of simian virus 40.

Authors:  J Martinis; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1978-05       Impact factor: 11.205

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  42 in total

1.  p53 shares an antigenic determinant with proteins of 92 and 150 kilodaltons that may be involved in senescence of human cells.

Authors:  S J van den Heuvel; S I The; B Klein; A G Jochemsen; A Zantema; A J van der Eb
Journal:  J Virol       Date:  1992-01       Impact factor: 5.103

2.  Repression of the basal c-fos promoter by wild-type p53.

Authors:  N Kley; R Y Chung; S Fay; J P Loeffler; B R Seizinger
Journal:  Nucleic Acids Res       Date:  1992-08-11       Impact factor: 16.971

3.  Anti-CHMP5 single chain variable fragment antibody retrovirus infection induces programmed cell death of AML leukemic cells in vitro.

Authors:  Hai-rong Wang; Zhen-yu Xiao; Miao Chen; Fei-long Wang; Jia Liu; Hua Zhong; Ji-hua Zhong; Ren-rong Ou-Yang; Yan-lin Shen; Shu-ming Pan
Journal:  Acta Pharmacol Sin       Date:  2012-05-21       Impact factor: 6.150

4.  The cellular secretory pathway is not utilized for biosynthesis, modification, or intracellular transport of the simian virus 40 large tumor antigen.

Authors:  D L Jarvis; W K Chan; M K Estes; J S Butel
Journal:  J Virol       Date:  1987-12       Impact factor: 5.103

5.  Antigenic binding sites of monoclonal antibodies specific for simian virus 40 large T antigen.

Authors:  E G Gurney; S Tamowski; W Deppert
Journal:  J Virol       Date:  1986-03       Impact factor: 5.103

6.  Extensive post-translational modification of active and inactivated forms of endogenous p53.

Authors:  Caroline J DeHart; Jasdave S Chahal; S J Flint; David H Perlman
Journal:  Mol Cell Proteomics       Date:  2013-09-20       Impact factor: 5.911

7.  Mammalian p53 can function as a transcription factor in yeast.

Authors:  E Schärer; R Iggo
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

8.  Tumor suppressor p53: analysis of wild-type and mutant p53 complexes.

Authors:  J Milner; E A Medcalf; A C Cook
Journal:  Mol Cell Biol       Date:  1991-01       Impact factor: 4.272

9.  Large T-antigen mutants define multiple steps in the initiation of simian virus 40 DNA replication.

Authors:  I J Mohr; M P Fairman; B Stillman; Y Gluzman
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

10.  P53 mutation in acute T cell lymphoblastic leukemia is of somatic origin and is stable during establishment of T cell acute lymphoblastic leukemia cell lines.

Authors:  J Yeargin; J Cheng; A L Yu; R Gjerset; M Bogart; M Haas
Journal:  J Clin Invest       Date:  1993-05       Impact factor: 14.808

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