Cationic Intrinsically Disordered Antimicrobial Peptides (CIDAMPs) Represent a New Paradigm of Innate Defense with a Potential for Novel Anti-Infectives.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
04 03 2019
Historique:
received: 18 10 2018
accepted: 19 12 2018
entrez: 6 3 2019
pubmed: 6 3 2019
medline: 21 10 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 30833614
doi: 10.1038/s41598-019-39219-w
pii: 10.1038/s41598-019-39219-w
pmc: PMC6399351
doi:

Substances chimiques

Anti-Infective Agents 0
Antimicrobial Cationic Peptides 0
Intrinsically Disordered Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3331

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom

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Auteurs

Ties Latendorf (T)

Department of Dermatology, University-Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Ulrich Gerstel (U)

Department of Dermatology, University-Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Zhihong Wu (Z)

Department of Dermatology, University-Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Institute of Biochemistry and Cell Biology, Zhejiang University of Science and Technology, 310023, Hangzhou, China.

Joachim Bartels (J)

Department of Dermatology, University-Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Alexander Becker (A)

Institute for Experimental Medicine-AG Systematic Proteomics & Bioanalytics, Kiel University (CAU), Kiel, Germany.

Andreas Tholey (A)

Institute for Experimental Medicine-AG Systematic Proteomics & Bioanalytics, Kiel University (CAU), Kiel, Germany.

Jens-Michael Schröder (JM)

Department of Dermatology, University-Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany. jschroeder@dermatology.uni-kiel.de.

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