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Novel inhibitors of surface layer processing in Clostridium difficile.

Research paper by T H TH Tam Dang, Robert P RP Fagan, Neil F NF Fairweather, Edward W EW Tate

Indexed on: 15 Jul '11Published on: 15 Jul '11Published in: Bioorganic & Medicinal Chemistry



Abstract

Clostridium difficile, a leading cause of hospital-acquired bacterial infection, is coated in a dense surface layer (S-layer) that is thought to provide both physicochemical protection and a scaffold for host-pathogen interactions. The key structural components of the S-layer are two proteins derived from a polypeptide precursor, SlpA, via proteolytic cleavage by the protease Cwp84. Here, we report the design, synthesis and in vivo characterization of a panel of protease inhibitors and activity-based probes (ABPs) designed to target S-layer processing in live C. difficile cells. Inhibitors based on substrate-mimetic peptides bearing a C-terminal Michael acceptor warhead were found to be promising candidates for further development.