{"title":"iAMY-RECMFF: Identifying amyloidgenic peptides by using residue pairwise energy content matrix and features fusion algorithm.","authors":"Zizheng Yu, Zhijian Yin, Hongliang Zou","doi":"10.1142/S0219720023500233","DOIUrl":null,"url":null,"abstract":"<p><p>Various diseases, including Huntington's disease, Alzheimer's disease, and Parkinson's disease, have been reported to be linked to amyloid. Therefore, it is crucial to distinguish amyloid from non-amyloid proteins or peptides. While experimental approaches are typically preferred, they are costly and time-consuming. In this study, we have developed a machine learning framework called iAMY-RECMFF to discriminate amyloidgenic from non-amyloidgenic peptides. In our model, we first encoded the peptide sequences using the residue pairwise energy content matrix. We then utilized Pearson's correlation coefficient and distance correlation to extract useful information from this matrix. Additionally, we employed an improved similarity network fusion algorithm to integrate features from different perspectives. The Fisher approach was adopted to select the optimal feature subset. Finally, the selected features were inputted into a support vector machine for identifying amyloidgenic peptides. Experimental results demonstrate that our proposed method significantly improves the identification of amyloidgenic peptides compared to existing predictors. This suggests that our method may serve as a powerful tool in identifying amyloidgenic peptides. To facilitate academic use, the dataset and codes used in the current study are accessible at https://figshare.com/articles/online_resource/iAMY-RECMFF/22816916.</p>","PeriodicalId":48910,"journal":{"name":"Journal of Bioinformatics and Computational Biology","volume":" ","pages":"2350023"},"PeriodicalIF":0.9000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bioinformatics and Computational Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1142/S0219720023500233","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/27 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Various diseases, including Huntington's disease, Alzheimer's disease, and Parkinson's disease, have been reported to be linked to amyloid. Therefore, it is crucial to distinguish amyloid from non-amyloid proteins or peptides. While experimental approaches are typically preferred, they are costly and time-consuming. In this study, we have developed a machine learning framework called iAMY-RECMFF to discriminate amyloidgenic from non-amyloidgenic peptides. In our model, we first encoded the peptide sequences using the residue pairwise energy content matrix. We then utilized Pearson's correlation coefficient and distance correlation to extract useful information from this matrix. Additionally, we employed an improved similarity network fusion algorithm to integrate features from different perspectives. The Fisher approach was adopted to select the optimal feature subset. Finally, the selected features were inputted into a support vector machine for identifying amyloidgenic peptides. Experimental results demonstrate that our proposed method significantly improves the identification of amyloidgenic peptides compared to existing predictors. This suggests that our method may serve as a powerful tool in identifying amyloidgenic peptides. To facilitate academic use, the dataset and codes used in the current study are accessible at https://figshare.com/articles/online_resource/iAMY-RECMFF/22816916.
期刊介绍:
The Journal of Bioinformatics and Computational Biology aims to publish high quality, original research articles, expository tutorial papers and review papers as well as short, critical comments on technical issues associated with the analysis of cellular information.
The research papers will be technical presentations of new assertions, discoveries and tools, intended for a narrower specialist community. The tutorials, reviews and critical commentary will be targeted at a broader readership of biologists who are interested in using computers but are not knowledgeable about scientific computing, and equally, computer scientists who have an interest in biology but are not familiar with current thrusts nor the language of biology. Such carefully chosen tutorials and articles should greatly accelerate the rate of entry of these new creative scientists into the field.