| Literature DB >> 26522134 |
Paul J Hensbergen1, Oleg I Klychnikov2, Dennis Bakker3, Irina Dragan2, Michelle L Kelly4, Nigel P Minton4, Jeroen Corver3, Ed J Kuijper3, Jan Wouter Drijfhout5, Hans C van Leeuwen6.
Abstract
The Clostridium difficile cd2830 gene product is a secreted metalloprotease, named Pro-Pro endopeptidase (PPEP-1). PPEP-1 cleaves C. difficile cell surface proteins (e.g. CD2831). Here, we confirmed that PPEP-1 has a unique preference for prolines surrounding the scissile bond. Moreover, we show that it exhibits a high preference for an asparagine at the P2 position and hydrophobic residues at the P3 position. Using a PPEP-1 knockout C. difficile strain, we demonstrate that the removal of the collagen binding protein CD2831 is fully attributable to PPEP-1 activity. The PPEP-1 knockout strain demonstrated higher affinity for collagen type I with attenuated virulence in hamsters.Entities:
Keywords: Adhesion; Bacterial virulence; Collagen binding; Motility; Secreted protease
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Year: 2015 PMID: 26522134 DOI: 10.1016/j.febslet.2015.10.027
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124