Literature DB >> 1648895

An unusual transmissible agent--MaTu.

J Závada1, Z Závadová.   

Abstract

MaTu is an agent, believed to be derived from a human mammary carcinoma, which displayed several extraordinary properties. These were: RIP and PAGE revealed in MaTu-infected cells only a single protein band of Mr 58 k, the gp 58. This gp 58 was immunoprecipitated by antibodies present in some human sera as well as in some sera of rabbits, sheep, and cattle. MaTu had an extremely restricted host range: it was transmissible only to HeLa cells, but not to human embryo fibroblasts, to three human tumour cell lines (T 47 D, T 24, and HMB 2) or to monkey Vero and rabbit SIRC cells. A retrovirus with a broad host range, used as a helper (X-MLV) enabled the transmission of MaTu to human fibroblasts, but not to Vero or SIRC, which are also permissive for X-MLV. These observations, together with our previous reports, support the view that MaTu might either be a novel type of defective virus, or even a non-viral autonomous genetic element.

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Year:  1991        PMID: 1648895     DOI: 10.1007/bf01314029

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  15 in total

1.  Rapid isolation of antigens from cells with a staphylococcal protein A-antibody adsorbent: parameters of the interaction of antibody-antigen complexes with protein A.

Authors:  S W Kessler
Journal:  J Immunol       Date:  1975-12       Impact factor: 5.422

2.  Pseudotypes of vesicular stomatitis virus with envelope antigens provided by murine mammary tumor virus.

Authors:  J Závada; C Dickson; R Weiss
Journal:  Virology       Date:  1977-10-01       Impact factor: 3.616

3.  Pseudotypes of vesicular stomatitis virus determined by exogenous and endogenous avian RNA tumor viruses.

Authors:  D N Love; R A Weiss
Journal:  Virology       Date:  1974-01       Impact factor: 3.616

4.  A transmissible antigen detected in two cell lines derived from human tumours.

Authors:  J Závada; Z Závadová; R Widmaier; J Bubeník; M Indrová; C Altaner
Journal:  J Gen Virol       Date:  1974-08       Impact factor: 3.891

5.  [A new infinite cell line, MaTu, of human mammary tumor-cells (author's transl)].

Authors:  R Widmaier; G P Wildner; G Papsdorf; I Graffi
Journal:  Arch Geschwulstforsch       Date:  1974

6.  Established cell line of urinary bladder carcinoma (T24) containing tumour-specific antigen.

Authors:  J Bubeník; M Baresová; V Viklický; J Jakoubková; H Sainerová; J Donner
Journal:  Int J Cancer       Date:  1973-05       Impact factor: 7.396

7.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

Review 8.  Viral pseudotypes and phenotypic mixing.

Authors:  J Závada
Journal:  Arch Virol       Date:  1976       Impact factor: 2.574

Review 9.  The pseudotypic paradox.

Authors:  J Závada
Journal:  J Gen Virol       Date:  1982-11       Impact factor: 3.891

10.  Humans have antibodies capable of recognizing oncoviral glycoproteins: demonstration that these antibodies are formed in response to cellular modification of glycoproteins rather than as consequence of exposure to virus.

Authors:  M Barbacid; D Bolognesi; S A Aaronson
Journal:  Proc Natl Acad Sci U S A       Date:  1980-03       Impact factor: 11.205

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  1 in total

1.  Molecular characterization of the genes coding for glycoprotein and L protein of lymphocytic choriomeningitis virus strain MX.

Authors:  Jana Tomaskova; Martina Labudova; Juraj Kopacek; Silvia Pastorekova; Jaromir Pastorek
Journal:  Virus Genes       Date:  2008-05-21       Impact factor: 2.332

  1 in total

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