期刊:Bioinformatics [Oxford University Press] 日期:2021-09-09卷期号:37 (17): 2556-2562被引量:21
标识
DOI:10.1093/bioinformatics/btab133
摘要
Motivation The identification of bitter peptides through experimental approaches is an expensive and time-consuming endeavor. Due to the huge number of newly available peptide sequences in the post-genomic era, the development of automated computational models for the identification of novel bitter peptides is highly desira-ble. Results In this work, we present BERT4Bitter, a bidirectional encoder representation from transformers (BERT)-based model for predicting bitter peptides directly from their amino acid sequence without using any structural information. To the best of our knowledge, this is the first time a BERT-based model has been employed to identify bitter peptides. Compared to widely used machine learning models, BERT4Bitter achieved the best performance with accuracy of 0.861 and 0.922 for cross-validation and independent tests, respectively. Furthermore, extensive empirical benchmarking experiments on the independent dataset demonstrated that BERT4Bitter clearly outperformed the existing method with improvements of > 8% accuracy and >16% Matthews coefficient correlation, highlighting the effectiveness and robustness of BERT4Bitter. We believe that the BERT4Bitter method proposed herein will be a useful tool for rapidly screening and identifying novel bitter peptides for drug development and nutritional research. Availability The user-friendly web server of the proposed BERT4Bitter is freely accessible at: http://pmlab.pythonanywhere.com/BERT4Bitter. Supplementary information Supplementary data are available at Bioinformatics online.