Engineering Approaches for the Development of Antimicrobial Peptide-Based Antibiotics

被引:28
作者
Kang, Su-Jin [1 ]
Nam, So Hee [1 ]
Lee, Bong-Jin [2 ]
机构
[1] Dongduk Womens Univ, Coll Pharm, Seoul 02748, South Korea
[2] Seoul Natl Univ, Coll Pharm, Res Inst Pharmaceut Sci, Seoul 08826, South Korea
来源
ANTIBIOTICS-BASEL | 2022年 / 11卷 / 10期
基金
新加坡国家研究基金会;
关键词
antimicrobial peptides (AMPs); multidrug-resistant (MDR) bacteria; antibiotics; engineering approaches; C-TERMINAL AMIDATION; ANTIBACTERIAL PEPTIDES; MODEL; NANOPARTICLES; CYTOTOXICITY; STABILITY; BACTERIA; DESIGN;
D O I
10.3390/antibiotics11101338
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Antimicrobial peptides (AMPs) have received increasing attention as potential alternatives for future antibiotics because of the rise of multidrug-resistant (MDR) bacteria. AMPs are small cationic peptides with broad-spectrum antibiotic activities and different action mechanisms to those of traditional antibiotics. Despite the desirable advantages of developing peptide-based antimicrobial agents, the clinical applications of AMPs are still limited because of their enzymatic degradation, toxicity, and selectivity. In this review, structural modifications, such as amino acid substitution, stapling, cyclization of peptides, and hybrid AMPs with conventional antibiotics or other peptides, will be presented. Additionally, nanodelivery systems using metals or lipids to deliver AMPs will be discussed based on the structural properties and action mechanisms of AMPs.
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页数:12
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