Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 117, Issue 32, Pages 19446-19454Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.2005540117
Keywords
antibiotic resistance; nephrotoxicity; NMR; peptide antibiotics; systemic efficacy
Categories
Funding
- National Institutes of Health [AI128230, AI105147]
- Nebraska Research Initiative Proof of Concept
- Agence Nationale de la Recherche [17-CE18-0033-3]
- Agence Nationale de la Recherche (LabEx Chemistry of Complex Systems)
- Reseau Thematique de Recherche Avancee International Center of Frontier Research in Chemistry
- India Raman Postdoctoral Fellowship
- Henan Visiting Scholarship
- China Scholarship Council
- Yangzhou University Scholarship
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Antimicrobial peptides are important candidates for developing new classes of antibiotics because of their potency against antibiotic-resistant pathogens. Current research focuses on topical applications and it is unclear how to design peptides with systemic efficacy. To address this problem, we designed two potent peptides by combining database-guided discovery with structure-based design. When bound to membranes, these two short peptides with an identical amino acid composition can adopt two distinct amphipathic structures: A classic horizontal helix (horine) and a novel vertical spiral structure (verine). Their horizontal and vertical orientations on membranes were determined by solid-state N-15 NMR data. While horine was potent primarily against gram-positive pathogens, verine showed broad-spectrum antimicrobial activity. Both peptides protected greater than 80% mice from infection-caused deaths. Moreover, horine and verine also displayed significant systemic efficacy in different murine models comparable to conventional antibiotics. In addition, they could eliminate resistant pathogens and preformed biofilms. Significantly, the peptides showed no nephrotoxicity to mice after intraperitoneal or intravenous administration for 1 wk. Our study underscores the significance of horine and verine in fighting drug-resistant pathogens.
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