Föreläsningar och seminarier

Immunology and Microbiology seminar: Cationic Intrinsically Disordered Antimicrobial Peptides (CIDAMPs) Represent a New Paradigm of Innate Defense with a Potential for Novel Anti-Infectives

2019-02-1813:00 Biomedicum B0313 3rd floor (Main entrance), Solna Campus.Campus SolnaBiomedicum

Speaker: Jens Schröder, Department of Dermatology, Venereology and Allergology, Kiel, Germany

Host: Katrin Pütsep

 

Abstract

Cationic Intrinsically Disordered Antimicrobial Peptides (CIDAMPs) Represent a New Paradigm of Innate Defense with a Potential for Novel Anti-Infectives
In the search for potential mechanisms underlying the remarkable resistance of healthy skin against infection by soil bacteria like Pseudomonas (P.) aeruginosa we identified fragments of the intrinsically disordered protein hornerin as potent microbicidal agents in the stratum corneum. We found that, independent of the amino acid (AA)-sequence, any tested linear cationic peptide containing a high percentage of disorder-promoting AA and a low percentage of order-promoting AA is a potent microbicidal antimicrobial. We further show that the antimicrobial activity of these cationic intrinsically disordered antimicrobial peptides (CIDAMPs) depends on the peptide chain length, its net charge, lipidation and environmental conditions. The ubiquitous presence of latent CIDAMP sources in nature suggests a common and yet overlooked adapted innate disinfection system of body surfaces. The simple structure and virtually any imaginable sequence or composition of disorder-promoting AA allow the generation of a plethora of CIDAMPs. These are potential novel microbicidal anti-infectives for various bacterial pathogens, including P. aeruginosa, methicillin-resistant Staphylococcus aureus (MRSA) and fungal pathogens like Candida albicans and Cryptococcus neoformans.

Recent publication

Hornerin contains a Linked Series of Ribosome-Targeting Peptide Antibiotics.
Gerstel U, Latendorf T, Bartels J, Becker A, Tholey A, Schröder J
Sci Rep 2018 Nov;8(1):16158

Contact person: Katrin Pütsep