{"title":"AFP-MCDF: Multi and cross-dimensional feature fusion methods for antifreeze protein prediction","authors":"Jinfeng Li, Fan Zhang, Zhenguo Wen, Chun Fang","doi":"10.1016/j.ab.2025.115881","DOIUrl":null,"url":null,"abstract":"<div><div>Antifreeze proteins can effectively inhibit the formation of ice crystals and enhance cell survival in low-temperature environments. They protect the texture prolong the shelf life of food and maintain cell and tissue integrity in medical treatments, thereby improving the success rate of surgery and transplantation. Accurate prediction of Antifreeze proteins is important to advance these fields. Traditional wet-experiment methods, while providing reliable validation results, are usually time-consuming and costly. And existing computational methods still have room for improvement in predicting performance. In this study, a novel antifreeze protein prediction method, AFP-MCDF, is proposed. The AFP-MCDF method first extracts one- and two-dimensional feature representations of Antifreeze protein sequences using the pre-trained protein language models ProtBERT and ESM-2. Subsequently, these features are fused multidimensionally via BiLSTM and TextCNN to capture long-term dependencies and local features. Finally, the method predicts the frost resistance of Antifreeze protein sequences by cross-dimensional fusion and linear mapping from N to 2 dimensions. Experimental results show that AFP-MCDF performs well in the antifreeze protein prediction task, outperforming traditional computational methods and reaching the current state-of-the-art.</div></div>","PeriodicalId":7830,"journal":{"name":"Analytical biochemistry","volume":"704 ","pages":"Article 115881"},"PeriodicalIF":2.6000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003269725001198","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Antifreeze proteins can effectively inhibit the formation of ice crystals and enhance cell survival in low-temperature environments. They protect the texture prolong the shelf life of food and maintain cell and tissue integrity in medical treatments, thereby improving the success rate of surgery and transplantation. Accurate prediction of Antifreeze proteins is important to advance these fields. Traditional wet-experiment methods, while providing reliable validation results, are usually time-consuming and costly. And existing computational methods still have room for improvement in predicting performance. In this study, a novel antifreeze protein prediction method, AFP-MCDF, is proposed. The AFP-MCDF method first extracts one- and two-dimensional feature representations of Antifreeze protein sequences using the pre-trained protein language models ProtBERT and ESM-2. Subsequently, these features are fused multidimensionally via BiLSTM and TextCNN to capture long-term dependencies and local features. Finally, the method predicts the frost resistance of Antifreeze protein sequences by cross-dimensional fusion and linear mapping from N to 2 dimensions. Experimental results show that AFP-MCDF performs well in the antifreeze protein prediction task, outperforming traditional computational methods and reaching the current state-of-the-art.
期刊介绍:
The journal''s title Analytical Biochemistry: Methods in the Biological Sciences declares its broad scope: methods for the basic biological sciences that include biochemistry, molecular genetics, cell biology, proteomics, immunology, bioinformatics and wherever the frontiers of research take the field.
The emphasis is on methods from the strictly analytical to the more preparative that would include novel approaches to protein purification as well as improvements in cell and organ culture. The actual techniques are equally inclusive ranging from aptamers to zymology.
The journal has been particularly active in:
-Analytical techniques for biological molecules-
Aptamer selection and utilization-
Biosensors-
Chromatography-
Cloning, sequencing and mutagenesis-
Electrochemical methods-
Electrophoresis-
Enzyme characterization methods-
Immunological approaches-
Mass spectrometry of proteins and nucleic acids-
Metabolomics-
Nano level techniques-
Optical spectroscopy in all its forms.
The journal is reluctant to include most drug and strictly clinical studies as there are more suitable publication platforms for these types of papers.