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PMID: 6169662 Published · ppublish English Journal Article

Surface proteins of simian-virus-40-transformed cells.

International journal of cancer ·Vol. 27 ·No. 3 ·1981-03-15 ·Pages 397-407

Chandrasekaran K, Winterbourne DJ, Luborsky SW, Mora PT

Abstract

Mammalian cells transformed in tissue culture by SV40 were shown to contain, in addition to the SV40-coded 94,000 d large T antigen and the 20,000 d small t antigen, a approximately 56,000 d cellular protein, which specifically precipitates with sera of animals bearing SV40-induced tumor(s) (tumor or T serum). We investigated the presence of these three proteins at the surface of logarithmically growing SV40-transformed cloned mouse cells, after metabolic labelling with [35S]-methionine for 3 h. The 56,000 d protein was found to be susceptible to digestion by trypsin under conditions which did not disrupt the cells, while no small t antigen was found to be digested. Both the 56,000 d cellular protein and the SV40 large T antigen were susceptible to lactoperoxidase-catalyzed iodination from the outside of intact cells. Trypsin treatment removed both the iodinated 56,000 d protein and the iodinated SV40 large T antigen. These experiments indicated that (a certain amount of) the 56,000 d protein and a relatively small amount of the large T antigen (which is present mainly in the nucleus) are present on the cell surface. The results confirm and extend independent experiments using subcellular fractionation techniques (Luborsky and Chandrasekaran, 1980; Soule and Butel, 1979). After heat treatment (at 50 degrees C for 30 min) of the whole-cell extract the 56,000 d cellular protein was precipitated by the tumor serum in the absence of precipitation of SV40 large T antigen. This result showed that the 56,000 d protein is more (thermo)stable (in the whole-cell extract) than the SV40 large T antigen, and also indicated that the tumor serum employed had antibodies against the 56,000 d cellular antigen. The heat-treated whole-cell extract of Sv40-transformed mouse cells was able to immunize and fully protect mice against a lethal tumorigenic dose of SV40-transformed cells. These results suggest the need for further experiments to characterize the chemical and immunologic properties of the 56,000 d protein.

MeSH Terms
Animals Antibodies, Neoplasm/immunology Antigens, Neoplasm/analysis Antigens, Viral Cell Line Cell Transformation, Viral Epitopes Membrane Proteins/analysis,immunology Mice Molecular Weight Neoplasms, Experimental/immunology Simian virus 40/immunology
Chemicals
Antibodies, Neoplasm Antigens, Neoplasm Antigens, Viral Epitopes Membrane Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chandrasekaran K
Winterbourne D J
Luborsky S W
Mora P T
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1981-03-15
Pages
397-407
Language
English
Region
United States
NLM ID
0042124
Subset
IM
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