deep-AMPpred: A Deep Learning Method for Identifying Antimicrobial Peptides and Their Functional Activities.

IF 5.6 2区 化学 Q1 CHEMISTRY, MEDICINAL
Jun Zhao, Hangcheng Liu, Leyao Kang, Wanling Gao, Quan Lu, Yuan Rao, Zhenyu Yue
{"title":"deep-AMPpred: A Deep Learning Method for Identifying Antimicrobial Peptides and Their Functional Activities.","authors":"Jun Zhao, Hangcheng Liu, Leyao Kang, Wanling Gao, Quan Lu, Yuan Rao, Zhenyu Yue","doi":"10.1021/acs.jcim.4c01913","DOIUrl":null,"url":null,"abstract":"<p><p>Antimicrobial peptides (AMPs) are small peptides that play an important role in disease defense. As the problem of pathogen resistance caused by the misuse of antibiotics intensifies, the identification of AMPs as alternatives to antibiotics has become a hot topic. Accurately identifying AMPs using computational methods has been a key issue in the field of bioinformatics in recent years. Although there are many machine learning-based AMP identification tools, most of them do not focus on or only focus on a few functional activities. Predicting the multiple activities of antimicrobial peptides can help discover candidate peptides with broad-spectrum antimicrobial ability. We propose a two-stage AMP predictor deep-AMPpred, in which the first stage distinguishes AMP from other peptides, and the second stage solves the multilabel problem of 13 common functional activities of AMP. deep-AMPpred combines the ESM-2 model to encode the features of AMP and integrates CNN, BiLSTM, and CBAM models to discover AMP and its functional activities. The ESM-2 model captures the global contextual features of the peptide sequence, while CNN, BiLSTM, and CBAM combine local feature extraction, long-term and short-term dependency modeling, and attention mechanisms to improve the performance of deep-AMPpred in AMP and its function prediction. Experimental results demonstrate that deep-AMPpred performs well in accurately identifying AMPs and predicting their functional activities. This confirms the effectiveness of using the ESM-2 model to capture meaningful peptide sequence features and integrating multiple deep learning models for AMP identification and activity prediction.</p>","PeriodicalId":44,"journal":{"name":"Journal of Chemical Information and Modeling ","volume":" ","pages":"997-1008"},"PeriodicalIF":5.6000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Information and Modeling ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.jcim.4c01913","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Antimicrobial peptides (AMPs) are small peptides that play an important role in disease defense. As the problem of pathogen resistance caused by the misuse of antibiotics intensifies, the identification of AMPs as alternatives to antibiotics has become a hot topic. Accurately identifying AMPs using computational methods has been a key issue in the field of bioinformatics in recent years. Although there are many machine learning-based AMP identification tools, most of them do not focus on or only focus on a few functional activities. Predicting the multiple activities of antimicrobial peptides can help discover candidate peptides with broad-spectrum antimicrobial ability. We propose a two-stage AMP predictor deep-AMPpred, in which the first stage distinguishes AMP from other peptides, and the second stage solves the multilabel problem of 13 common functional activities of AMP. deep-AMPpred combines the ESM-2 model to encode the features of AMP and integrates CNN, BiLSTM, and CBAM models to discover AMP and its functional activities. The ESM-2 model captures the global contextual features of the peptide sequence, while CNN, BiLSTM, and CBAM combine local feature extraction, long-term and short-term dependency modeling, and attention mechanisms to improve the performance of deep-AMPpred in AMP and its function prediction. Experimental results demonstrate that deep-AMPpred performs well in accurately identifying AMPs and predicting their functional activities. This confirms the effectiveness of using the ESM-2 model to capture meaningful peptide sequence features and integrating multiple deep learning models for AMP identification and activity prediction.

Deep - amppred:一种识别抗菌肽及其功能活性的深度学习方法。
抗菌肽是一种在疾病防御中起重要作用的小肽。随着抗生素滥用引起的病原菌耐药问题的加剧,抗菌肽作为抗生素替代品的鉴定已成为研究热点。近年来,利用计算方法准确识别amp已成为生物信息学领域的一个关键问题。虽然有很多基于机器学习的AMP识别工具,但大多数都不关注或只关注少数功能活动。预测抗菌肽的多种活性有助于发现具有广谱抗菌能力的候选肽。我们提出了一个两阶段的AMP预测器deep-AMPpred,其中第一步将AMP与其他肽区区分,第二阶段解决AMP 13种常见功能活性的多标签问题。deep-AMPpred结合ESM-2模型对AMP的特征进行编码,并集成CNN、BiLSTM和CBAM模型来发现AMP及其功能活性。ESM-2模型捕获了肽序列的全局上下文特征,而CNN、BiLSTM和CBAM结合了局部特征提取、长期和短期依赖建模以及注意机制,提高了deep-AMPpred在AMP及其功能预测中的性能。实验结果表明,deep-AMPpred在准确识别amp和预测其功能活性方面具有良好的性能。这证实了使用ESM-2模型捕获有意义的肽序列特征和集成多个深度学习模型进行AMP识别和活性预测的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信