Machine learning and genetic algorithm-guided directed evolution for the development of antimicrobial peptides

被引:6
|
作者
Zhang, Heqian [1 ]
Wang, Yihan [1 ]
Zhu, Yanran [1 ]
Huang, Pengtao [1 ]
Gao, Qiandi [1 ]
Li, Xiaojie [1 ]
Chen, Zhaoying [1 ]
Liu, Yu [2 ]
Jiang, Jiakun [3 ]
Gao, Yuan [4 ]
Huang, Jiaquan [1 ]
Qin, Zhiwei [1 ]
机构
[1] Beijing Normal Univ, Adv Inst Nat Sci, Ctr Biol Sci & Technol, Zhuhai 519087, Guangdong, Peoples R China
[2] Beijing Normal Univ, Adv Inst Nat Sci, Int Acad Ctr Complex Syst, Zhuhai 519087, Guangdong, Peoples R China
[3] Beijing Normal Univ, Adv Inst Nat Sci, Ctr Stat & Data Sci, Zhuhai 519087, Guangdong, Peoples R China
[4] Beijing Normal Univ, Instrumentat & Serv Ctr Sci & Technol, Zhuhai 519087, Guangdong, Peoples R China
关键词
Machine learning; Genetic algorithm; Directed evolution; Antimicrobial peptide; BLACK TIGER SHRIMP; ANTILIPOPOLYSACCHARIDE FACTOR ALF; TORSION ANGLE DYNAMICS; PENAEUS-MONODON; NMR STRUCTURE; SEQUENCE; IDENTIFICATION; PROGRAM; MODEL; DERMASEPTINS;
D O I
10.1016/j.jare.2024.02.016
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Antimicrobial peptides (AMPs) are valuable alternatives to traditional antibiotics, possess a variety of potent biological activities and exhibit immunomodulatory effects that alleviate difficult-to- treat infections. Clarifying the structure-activity relationships of AMPs can direct the synthesis of desirable peptide therapeutics. Objectives: In this study, the lipopolysaccharide-binding domain (LBD) was identified through machine learning-guided directed evolution, which acts as a functional domain of the anti-lipopolysaccharide factor family of AMPs identified from Marsupenaeus japonicus. Methods: LBDA-D was identified as an output of this algorithm, in which the original LBDMj sequence was the input, and the three-dimensional solution structure of LBDB was determined using nuclear magnetic resonance. Furthermore, our study involved a comprehensive series of experiments, including morphological studies and in vitro and in vivo antibacterial tests. Results: The NMR solution structure showed that LBDB possesses a circular extended structure with a disulfide crosslink at the terminus and two 310-helices and exhibits a broad antimicrobial spectrum. In addition, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that LBDB induced the formation of a cluster of bacteria wrapped in a flexible coating that ruptured and consequently killed the bacteria. Finally, coinjection of LBDB, Vibrio alginolyticus and Staphylococcus aureus in vivo improved the survival of M. japonicus, demonstrating the promising therapeutic role of LBDB for treating infectious disease. Conclusions: The findings of this study pave the way for the rational drug design of activity-enhanced peptide antibiotics. (c) 2023 The Authors. Published by Elsevier B.V. on behalf of Cairo University This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:415 / 428
页数:14
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