Enhanced binding to origin DNA at low pH enables easy detection of polyomavirus large T antigen by gel mobility shift assay of unfixed complexes-Reference-Cited by-同舟云学术

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Enhanced binding to origin DNA at low pH enables easy detection of polyomavirus large T antigen by gel mobility shift assay of unfixed complexes

Published:1999-03 Issue:1-2 Volume:78 Page:13-19
ISSN:0166-0934
Container-title:Journal of Virological Methods
language:en
Short-container-title:Journal of Virological Methods

Author:

Peng Yu-Cai,Acheson Nicholas H.

Publisher

Elsevier BV

Subject

Virology

Reference33 articles.

1. Stalling by RNA polymerase II in the polyomavirus intergenic region is dependent on functional large T antigen;Bertin;Virology,1992

2. Mutation of large T-antigen-binding site A, but not site B or C, eliminates stalling by RNA polymerase II in the intergenic region of polyomavirus DNA;Bertin;J. Virol.,1993

3. Murine polyomavirus and simian virus 40 large T antigens produce different structural alterations in viral origin DNA;Bhattacharyya;J. Virol.,1995

4. Preferred DNA-binding-sites of polyomavirus large T-antigen;Bondeson;Eur. J. Biochem.,1995

5. DNA binding of polyomavirus large T-antigen: kinetics of interactions with different types of binding sites;Bondeson;FEBS Lett.,1998

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