This item is only available for download by members of the University of Illinois community. Students, faculty, and staff at the U of I may log in with your NetID and password to view the item. If you are trying to access an Illinois-restricted dissertation or thesis, you can request a copy through your library's Inter-Library Loan office or purchase a copy directly from ProQuest.
Permalink
https://hdl.handle.net/2142/67414
Description
Title
Characterization of Tumorigenic Proteins
Author(s)
Stitt, David Thomas
Issue Date
1981
Department of Study
Biochemistry
Discipline
Biochemistry
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Chemistry, Biochemistry
Language
eng
Abstract
The 17K, 84K, and 94K SV40 T antigens from SV40 permissive and transformed cells were analyzed by tryptic peptide mapping on ion exchange columns. The tryptic peptides were mapped relative to the SV40 DNA and to their known functions. The aminotermini of the 17K, 84K and 94K T antigens are identical. The 84K protein probably arises from the 94K T antigen by proteolytic cleavage of the 94K T antigen carboxyterminus. The 48K and 55K nonviral antigens, proteins immunoprecipitable by SV40 T antibody from SV40 permissive and transformed cells, were compared to the SV40 large T antigen and to each other by tryptic peptide mapping. The 48K and 55K nonviral antigens are not degradation products of the SV40 T antigens and at most are only slightly related to the SV40 T antigens. The 48K and 55K nonviral antigens are slightly related to each other, sharing about 3 methionine containing tryptic peptides. Four SV40 transformed human cell lines, one SV40 transformed mouse cell line, and eight SV40 transformed human/mouse somatic cell hybrid cell lines were examined for the expression of nonviral antigens. Differences were found in the patterns of expression of the nonviral antigens among the human cell lines, between the human and the mouse cell lines, and between the human/mouse somatic cell hybrid cell lines and the human lines from which they were derived. Two of the human cell lines expressed only a 55K nonviral antigen; two expressed both 55K nonviral antigen; two expressed both 55K and 52K nonviral antigens. The mouse cell line expressed both a 55K and a 48K nonviral antigen, except for one. The Balb IV-8 cell line expressed 55K and 52K nonviral antigens. By comparing the tryptic peptides fractionated on cation exchange columns of the nonviral antigens it was determined that: (1) The 48K nonviral antigen in human/mouse hybrids is encoded by a mouse chromosome. (2) The 52K nonviral antigen in the Balb IV-8 human/mouse hybrid is encoded by a mouse chromosome and is probably a precursor to the mouse 48K nonviral antigen. (3) The 55K nonviral antigen in the C57-VII-6 human/mouse hybrid is encoded by a human chromosome; while in the Balb IV-8 human/mouse hybrid the 55K protein band is encoded by a human chromosome and probably by a mouse chromosome also. (4) If the gene encoding the human nonviral antigen is located on a single chromosome, it is located on human chromosome 7.
Use this login method if you
don't
have an
@illinois.edu
email address.
(Oops, I do have one)
IDEALS migrated to a new platform on June 23, 2022. If you created
your account prior to this date, you will have to reset your password
using the forgot-password link below.