Solution structure and antibacterial mechanism of two synthetic antimicrobial peptides.
- Author:
Lin YANG
1
;
Meihua FAN
;
Xuezhu LIU
;
Mei WU
;
Ge SHI
;
Zhi LIAO
Author Information
1. Laboratory of Marine Biology and Molecular Engineering, College of Marine Science, Zhejiang Ocean University, Zhoushan 316004, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Anti-Infective Agents;
chemical synthesis;
pharmacology;
Antimicrobial Cationic Peptides;
chemical synthesis;
chemistry;
pharmacology;
Cell Wall;
drug effects;
Escherichia coli;
drug effects;
Mytilus;
chemistry;
Sarcina;
drug effects
- From:
Chinese Journal of Biotechnology
2011;27(11):1564-1573
- CountryChina
- Language:Chinese
-
Abstract:
Mytilin-derived-peptide-1 (MDP-1) and mytilin-derived-peptide-2 (MDP-2) are two truncated decapeptides with reversed sequence synthesized corresponding to the residues 20-29 of mytilin-1 (GenBank Accession No. FJ973154) from M. coruscus. The objective of this study is to characterize the structural basis of these two peptides for their antimicrobial activities and functional differences, and to investigate the inhibitory mechanism of MDPs on Escherichia coli and Sarcina lutea. The structures of MDP-1 and MDP-2 in solution were determined by 1H 2D NMR methods; the antibactericidal effects of MDPs on E. coli and S. lutea were observed by transmitted electron microscopy (TEM). Both MDP-1 and MDP-2 have a well-defined loop structure stabilized by two additional disulfide bridges, which resemble the-hairpin structure of mytilin-1 model. The surface profile of MDPs' structures was characterized by protruding charged residues surrounded by hydrophobic residues. TEM analysis showed that MDPs destroyed cytoplasmic membrane and cell wall of bacteria and the interface between the cell wall and membrane was blurred. Furthermore, some holes were observed in treated bacteria, which resulted in cell death. Structural comparison between MDP-1 and MDP-2 shows that the distribution of positively charged amino acids on the loop of MDPs is topologically different significantly, which might be the reason why MDP-2 has higher activity than MDP-1. Furthermore, TEM results suggested that the bactericidal mechanisms of MDPs against E. coli and S. lutea were similar. Both MDP-1 and MDP-2 could attach to the negatively charged bacterial wall by positively charged amino acid residues and destroy the bacteria membrane in a pore-forming manner, thus cause the contents of the cells to release and eventually cell death.
