Expression of polyoma early gene products in E. coli

Brian Schaffhausen, Thomas L. Benjamin, Jennifer Lodge, David Kaplan, Thomas M. Roberts

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

The three products of the early region of polyoma virus have been cloned for expression in E. coli using the Tac promoter. Although the identical promoter and ribosome binding site are used in each final construction, the observed level of protein expression is different for each protein. While plasmids expressing wild type T antigens as well as a plasmid expressing the truncated Py-1387T middle T antigen lacking the membrane-anchoring sequence give rise to synthesis of proteins readily detectible by 95S-methionine labeling and immunoprecipitation, only small P and the middle T of Py-1387T are made in amounts sufficient for ready detection in total cell protein. Unlike middle T expressed in animal cells, middle T produced in E. coli is not detectibly phosphorylated. Further, the E. coli protein lacks tyrosine kinase activity.

Original languageEnglish
Pages (from-to)501-519
Number of pages19
JournalNucleic acids research
Volume13
Issue number2
DOIs
StatePublished - Jan 25 1985
Externally publishedYes

Fingerprint Dive into the research topics of 'Expression of polyoma early gene products in E. coli'. Together they form a unique fingerprint.

  • Cite this

    Schaffhausen, B., Benjamin, T. L., Lodge, J., Kaplan, D., & Roberts, T. M. (1985). Expression of polyoma early gene products in E. coli. Nucleic acids research, 13(2), 501-519. https://doi.org/10.1093/nar/13.2.501