4.8 Article

Dual-Mechanism Glycolipidpeptide with High Antimicrobial Activity, Immunomodulatory Activity, and Potential Application for Combined Antibacterial Therapy

Journal

ACS NANO
Volume 17, Issue 7, Pages 6292-6316

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c10249

Keywords

antimicrobial peptides; glycolipidpeptide; membrane penetrating activity; SPase I; nanomedicine

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Bacterial drug resistance poses a serious threat, necessitating the development of effective antibacterial drugs. This study focused on the design and synthesis of glycolipidpeptides with excellent antibacterial and immunomodulatory activities, which exhibited sustained-release properties and combined sterilization effects. The results demonstrate the potential applications of this research.
Bacterial drug resistance is becoming increasingly serious, and it is urgent to develop effective antibacterial drugs. Antimicrobial peptides (AMPs), as potential candidates against bacteria, have a broad prospect for development. Herein, a series of AMPs with biological characteristics (net positive charge, amphiphilicity, and alpha-helix), an AXA motif recognized by membrane bound serine protease type I signal peptidases ( SPase I), an FLPII motif to reduce hemolysis, and a monosaccharide motif to improve the stability and activity were designed and synthesized, and among which, the glycolipidpeptide GLP6 (glycosylated LP6 lipopeptide) had excellent antibacterial and immunomodulatory activity, good stability and biocompatibility, and excellent biofilm eradication and membrane penetrating activity. The positively charged spherical aggregates formed by self-assembly of GLP6 could encapsulate tetracycline (TC) to form GLP6@TC with a sustained-release effect, which could enhance the sensitivity of bacteria to the antibiotic and realize combined sterilization. The results of acute peritonitis and bacterial keratitis showed that GLP6@TC had a good combined antibacterial effect and the ability to inhibit interleukin-2 (IL-2), which could significantly reduce the inflammatory response while treating bacterial infection, and it had great potential for application. The results of computer molecular docking showed the AXA motif could effectively bind to SPase I, which was consistent with the results of biological experiments. In general, the study could provide a perspective for the design of AMPs and combined antibacterial therapy.

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