The Modification and Design of Antimicrobial Peptide

被引:41
|
作者
Gao, Yidan [1 ]
Fang, Hengtong [1 ]
Fang, Lu [1 ]
Liu, Dawei [2 ]
Liu, Jinsong [1 ]
Su, Menghan [1 ]
Fang, Zhi [3 ]
Ren, Wenzhi [1 ]
Jiao, Huping [1 ]
机构
[1] Jilin Univ, Coll Anim Sci, 5333 Xian Rd, Changchun 130062, Jilin, Peoples R China
[2] Ctr Dis Control & Prevent, Jinan Mil Area, 36 East Wenhua Rd, Jinan, Shandong, Peoples R China
[3] Cadres Sanat Tianjin, 7 Yuhong Rd, Tianjin, Peoples R China
关键词
Amino acids; infectious disease; antibiotics; modification; design; antimicrobial peptide; MOLECULAR-DYNAMICS SIMULATIONS; GOLD-NANOPARTICLES; STAPHYLOCOCCUS-AUREUS; IN-VIVO; ANTIBACTERIAL ACTIVITY; PHAGE DISPLAY; 70S RIBOSOME; PEGYLATION; CELLS; ANTIBIOTICS;
D O I
10.2174/1381612824666180213130318
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The antimicrobial peptides (AMPs) are a group of unique naturally occurring anti-microbial compounds with around 50 amino acids. It represents promising therapeutic agents to the infectious disease without concerning about drug resistance. However, commercial development of these peptides for even the simplest application has been hindered by the limitations of sources, instability, toxicity and bioavailability. To improve the properties of the artificial synthesized AMPs, the modification and design are the hotspots of the AMPs research. In fact, more than half of the known AMPs are naturally modified. In this review, two types of modification strategies, biochemical modification and chemical modification were summarized. Although, the chemical modification is versatile and direct, the manufacturing cost is greatly increased compared to the antibiotics. With the recent progress of the protein modification enzyme, the biochemical modification of the antimicrobial peptide followed by heterologous expression has great application prospects.
引用
收藏
页码:904 / 910
页数:7
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