Bacterial protein toxins inhibiting low-molecular-mass GTP-binding proteins

Citation
I. Just et al., Bacterial protein toxins inhibiting low-molecular-mass GTP-binding proteins, INT J MED M, 291(4), 2001, pp. 243-250
Citations number
59
Categorie Soggetti
Microbiology
Journal title
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY
ISSN journal
14384221 → ACNP
Volume
291
Issue
4
Year of publication
2001
Pages
243 - 250
Database
ISI
SICI code
1438-4221(200109)291:4<243:BPTILG>2.0.ZU;2-J
Abstract
The Rho GTPases, which belong to the Ras superfamily of low-molecular-mass GTP-binding proteins, are the preferred intracellular targets of bacterial protein toxins. The Rho GTPases RhoA/B/C, Rac1/2 and Cdc42 are the master r egulators of the actin cytoskeleton. Clostridium difficile toxins A and B, the causative agents of the antibiotic-associated pseudomembranous colitis, are intracellularly acting cytotoxins which mono-glucosylate the Rho GTPas es. Clostridium botulinum C3 toxin, which is not related to the clostridial neurotoxins, catalyses ADP-ribosylation of RhoA/B/C but not of other Rho G TPases. Glucosylation as well as ADP-ribosylation result in functional inac tivation of Rho causing disassembly of the actin cytoskeleton.