3zjx

Clostridium perfringens epsilon toxin mutant H149A bound to octyl glucoside

spinqualitylabelsall models 3zjx, resolution 2.40Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 3zjx is a 4 chain structure with sequence from Clostridium perfringens D. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 2.4Å Ligands: BOG, PO4 Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function E7D8R1_CLOPF Publication Abstract from PubMed Clostridium perfringens epsilon toxin (Etx) is a pore-forming toxin responsible for a severe and rapidly fatal enterotoxemia of ruminants. The toxin is classified as a category B bioterrorism agent by the U.S. Government Centres for Disease Control and Prevention (CDC), making work with recombinant toxin difficult. To reduce the hazard posed by work with recombinant Etx, we have used a variant of Etx that contains a H149A mutation (Etx-H149A), previously reported to have reduced, but not abolished, toxicity. The 3D structure of H149A prototoxin shows that the H149A mutation in domain III does not affect organisation of the putative receptor binding loops in domain I of the toxin. Surface exposed tyrosine residues in domain I of Etx-H149A (Y16, Y20, Y29, Y30, Y36 and Y196) were mutated to alanine and mutants Y30A and Y196A showed significantly reduced binding to MDCK.2 cells relative to Etx-H149A that correlated with their reduced cytotoxic activity. Thus, our study confirms the role of surface exposed tyrosine residues in domain I of Etx in binding to MDCK cells and the suitability of Etx-H149A for further receptor binding studies. In contrast, binding of all of the tyrosine mutants to ACHN cells was similar to that of Etx-H149A, suggesting that Etx can recognise different cell surface receptors. In support of this, the crystal structure of Etx-H149A identified a glycan (beta-octyl-glucoside) binding site in domain III of Etx-H149A, which may be a second receptor binding site. These findings have important implications for developing strategies designed to neutralise toxin activity. Clostridium perfringens epsilon toxin H149A mutant as a platform for receptor binding studies.,Bokori-Brown M, Kokkinidou MC, Savva CG, da Costa SP, Naylor CE, Cole AR, Moss DS, Basak AK, Titball RW Protein Sci. 2013 Mar 18. doi: 10.1002/pro.2250. PMID:23504825 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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