An efficient hybrid deep learning architecture for predicting short antimicrobial peptides

Abstract

Short‐length antimicrobial peptides (AMPs) have been demonstrated to have intensified antimicrobial activities against a wide spectrum of microbes. Therefore, exploration of novel and promising short AMPs is highly essential in developing various types of antimicrobial drugs or treatments. In addition to experimental approaches, computational methods have been developed to improve screening efficiency. Although existing computational methods have achieved satisfactory performance, there is still much room for model improvement. In this study, we proposed iAMP‐DL, an efficient hybrid deep learning architecture, for predicting short AMPs. The model was constructed using two well‐known deep learning architectures: the long short‐term memory architecture and convolutional neural networks. To fairly assess the performance of the model, we compared our model with existing state‐of‐the‐art methods using the same independent test set. Our comparative analysis shows that iAMP‐DL outperformed other methods. Furthermore, to assess the robustness and stability of our model, the experiments were repeated 10 times to observe the variation in prediction efficiency. The results demonstrate that iAMP‐DL is an effective, robust, and stable framework for detecting promising short AMPs. Another comparative study of different negative data sampling methods also confirms the effectiveness of our method and demonstrates that it can also be used to develop a robust model for predicting AMPs in general. The proposed framework was also deployed as an online web server with a user‐friendly interface to support the research community in identifying short AMPs.