4.7 Article

Deep-ABPpred: identifying antibacterial peptides in protein sequences using bidirectional LSTM with word2vec

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 5, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab065

关键词

AMR; antibacterial peptides; deep learning; BiLSTM; Streptococcus; bacteriophage

资金

  1. National Agricultural Science Fund (NASF) [NASF/ABA-6014/2016-17/367]

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The study introduces Deep-ABPpred, a deep learning classifier for identifying ABPs in protein sequences, which outperforms other state-of-the-art classifiers. This model shows high precision and applicability in proposing and synthesizing novel ABPs for experimentation. Deep-ABPpred demonstrates the capability of identifying potent antibacterial peptides in protein sequences, confirming its potential impact in the field of antimicrobial research.
The overuse of antibiotics has led to emergence of antimicrobial resistance, and as a result, antibacterial peptides (ABPs) are receiving significant attention as an alternative. Identification of effective ABPs in lab from natural sources is a cost-intensive and time-consuming process. Therefore, there is a need for the development of in silico models, which can identify novel ABPs in protein sequences for chemical synthesis and testing. In this study, we propose a deep learning classifier named Deep-ABPpred that can identify ABPs in protein sequences. We developed Deep-ABPpred using bidirectional long short-term memory algorithm with amino acid level features from word2vec. The results show that Deep-ABPpred outperforms other state-of-the-art ABP classifiers on both test and independent datasets. Our proposed model achieved the precision of approximately 97 and 94% on test dataset and independent dataset, respectively. The high precision suggests applicability of Deep-ABPpred in proposing novel ABPs for synthesis and experimentation. By utilizing Deep-ABPpred, we identified ABPs in the tail protein sequences of Streptococcus bacteriophages, chemically synthesized identified peptides in lab and tested their activity in vitro. These ABPs showed potent antibacterial activity against selected Gram-positive and Gram-negative bacteria, which confirms the capability of Deep-ABPpred in identifying novel ABPs in protein sequences. Based on the proposed approach, an online prediction server is also developed, which is freely accessible at https://abppred.anvil.app/. This web server takes the protein sequence as input and provides ABPs with high probability (>0.95) as output.

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