Abstract
Simian virus 40 small-t and large-T antigen were synthesized in vitro and labeled with methionine donated by initiator tRNA. Tryptic peptide fingerprinting was used to identify the amino-terminal peptide of the two proteins. Similar fingerprint analysis of small-t and large-T made in vitro in the absence of acetyl coenzyme A showed that the mobility of the amino-terminal peptide was changed under these conditions and suggested that it is acetylated. These data establish that the amino-terminal methionine residue of simian virus 40 small-t and large-T results from an initiation event, not post-translational cleavage, and provides additional evidence that the amino terminus of both proteins is acetylated. The identification of the amino-terminal peptide provides a useful marker for further studies on different forms of T-antigen from cells infected with and transformed by simian virus 40 and related viruses.
Original language | English (US) |
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Pages (from-to) | 992-996 |
Number of pages | 5 |
Journal | Journal of Virology |
Volume | 28 |
Issue number | 3 |
DOIs | |
State | Published - 1978 |
ASJC Scopus subject areas
- Microbiology
- Immunology
- Insect Science
- Virology