Related Experiment Video
Updated: Jun 5, 2026

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
Published on: January 3, 2012
Cholera- and anthrax-like toxins are among several new ADP-ribosyltransferases
Robert J Fieldhouse1, Zachari Turgeon, Dawn White
1Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.
Abstract:
Chelt, a cholera-like toxin from Vibrio cholerae, and Certhrax, an anthrax-like toxin from Bacillus cereus, are among six new bacterial protein toxins we identified and characterized using in silico and cell-based techniques. We also uncovered medically relevant toxins from Mycobacterium avium and Enterococcus faecalis. We found agriculturally relevant toxins in Photorhabdus luminescens and Vibrio splendidus. These toxins belong to the ADP-ribosyltransferase family that has conserved structure despite low sequence identity. Therefore, our search for new toxins combined fold recognition with rules for filtering sequences--including a primary sequence pattern--to reduce reliance on sequence identity and identify toxins using structure. We used computers to build models and analyzed each new toxin to understand features including: structure, secretion, cell entry, activation, NAD+ substrate binding, intracellular target binding and the reaction mechanism. We confirmed activity using a yeast growth test. In this era where an expanding protein structure library complements abundant protein sequence data--and we need high-throughput validation--our approach provides insight into the newest toxin ADP-ribosyltransferases.
Related Concept Videos
Bacterial Toxins
Bacterial Gastroenteritis
GPCRs Regulate Adenylyl Cylase Activity
Two...
Cholera
Gram-negative Bacterial Protein Secretion Systems
Tail-anchoring of Proteins in the ER Membrane

