Plectasin, a Fungal Defensin, Targets the Bacterial Cell Wall Precursor Lipid II

Author:

Schneider Tanja1,Kruse Thomas2,Wimmer Reinhard3,Wiedemann Imke1,Sass Vera1,Pag Ulrike1,Jansen Andrea1,Nielsen Allan K.4,Mygind Per H.4,Raventós Dorotea S.4,Neve Søren4,Ravn Birthe4,Bonvin Alexandre M. J. J.5,De Maria Leonardo4,Andersen Anders S.24,Gammelgaard Lora K.4,Sahl Hans-Georg1,Kristensen Hans-Henrik4

Affiliation:

1. Pharmaceutical Microbiology Section, Institute for Medical Microbiology, Immunology, and Parasitology, University of Bonn, D-53115 Bonn, Germany.

2. Statens Serum Institut, 2300 Copenhagen S, Denmark.

3. Department of Biotechnology, Chemistry, and Environmental Engineering, Aalborg University, DK-9000 Aalborg, Denmark.

4. Novozymes AS, DK-2880 Bagsvaerd, Denmark.

5. Department of Chemistry, Faculty of Science, Utrecht University, 3584 CH Utrecht, Netherlands.

Abstract

Defining Defensins' Mode of Action Defensins are antimicrobial host defense peptides that play a role in innate immunity. Many such peptides act by disrupting the bacterial membrane; however, Schneider et al. (p. 1168 ) now show that the fungal defensin, plecstasin, targets cell wall biosynthesis. Biochemical studies identified Lipid II as the cellular target of plecstasin and the residues involved in complex formation were identified using NMR spectroscopy and computational modeling. Initial studies identified two defensins from invertebrates that also target Lipid II. Plecstasin is active against some drug-resistant Gram-positive bacteria, and its action against a validated target makes it a promising lead for further drug development.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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