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Purification and Characterization of Yersinia enterocolitica and Yersinia pestis LcrV–Cholera Toxin A2/B Chimeras
Protein Expression and Purification
  • Juliette K. Tinker, Boise State University
  • Chadwick T. Davis, Boise State University
  • Britni M. Arlian, Boise State University
Document Type
Article
Publication Date
11-1-2010
Disciplines
Abstract
Yersinia pestis is a virulent human pathogen and potential biological weapon. Despite a long history of research on this organism, there is no licensed vaccine to protect against pneumonic forms of Y. pestis disease. In the present study, plasmids were constructed to express cholera toxin A2/B chimeric molecules containing the LcrV protective antigen from Yersinia enterocolitica and Y. pestis. These chimeras were expressed and purified to high yields from the supernatant of transformed Escherichia coli. Western and GM1 ELISA assays were used to characterize the composition, receptor-binding and relative stability of the LcrV–CTA2/B chimera in comparison to cholera toxin. In addition, we investigated the ability of the Y. pestis LcrV–CTA2/B chimera to bind to and internalize into cultured epithelial cells and macrophages by confocal microscopy. These studies indicate that the uptake and trafficking of the LcrV antigen from the chimera is comparable to the trafficking of native toxin. Together these findings report that stable, receptor-binding, non-toxic LcrV–cholera toxin A2/B chimeras can be expressed at high levels in E. coli and purified from the supernatant. In addition, the internalization of antigen in vitro reported here supports the development of these molecules as novel mucosal vaccine candidates.
Citation Information
Juliette K. Tinker, Chadwick T. Davis and Britni M. Arlian. "Purification and Characterization of Yersinia enterocolitica and Yersinia pestis LcrV–Cholera Toxin A2/B Chimeras" Protein Expression and Purification (2010)
Available at: http://works.bepress.com/juliette_tinker/2/