{"title":"基于蛋白质语言模型验证 SARSCov-2 中 Omicron 系的独特性","authors":"Ke Dong, Jingyang Gao","doi":"10.2174/0115748936291075240409080924","DOIUrl":null,"url":null,"abstract":"Introduction: Variants of concern were identified in severe acute respiratory syndrome coronavirus 2, namely Alpha, Beta, Gamma, Delta, and Omicron. This study explores the mutations of the Omicron lineage and its differences from other lineages through a protein language model. Methods: By inputting the severe acute respiratory syndrome coronavirus 2 wild-type sequence into the protein language model evolving pre-trained models-1v, this study obtained the score for each position mutating to other amino acids and calculated the overall trend of a new variant of concern mutation scores. objective: Analyze the differences in the number of Omicron amino acid mutations compared to the other four VOC mutations using statistical methods, and use the protein language model esm-1v to analyze the specificity of Omicron amino acid mutations. Results: It is found that when the proportion of unobserved mutations to observed mutations is 4:15, Omicron still generates a large number of newly emerging mutations. It was found that the overall score for the Omicron family is low, and the overall ranking for the Omicron family is low. Conclusion: Mutations in the Omicron lineage are different from amino acid mutations in other lineages. The findings of this paper deepen the understanding of the spatial distribution of spike protein amino acid mutations and overall trends of newly emerging mutations corresponding to different variants of concern. This also provides insights into simulating the evolution of the Omicron lineage.","PeriodicalId":10801,"journal":{"name":"Current Bioinformatics","volume":"63 1","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2024-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Validating the Distinctiveness of the Omicron Lineage within the SARSCov-2 based on Protein Language Models\",\"authors\":\"Ke Dong, Jingyang Gao\",\"doi\":\"10.2174/0115748936291075240409080924\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Variants of concern were identified in severe acute respiratory syndrome coronavirus 2, namely Alpha, Beta, Gamma, Delta, and Omicron. This study explores the mutations of the Omicron lineage and its differences from other lineages through a protein language model. Methods: By inputting the severe acute respiratory syndrome coronavirus 2 wild-type sequence into the protein language model evolving pre-trained models-1v, this study obtained the score for each position mutating to other amino acids and calculated the overall trend of a new variant of concern mutation scores. objective: Analyze the differences in the number of Omicron amino acid mutations compared to the other four VOC mutations using statistical methods, and use the protein language model esm-1v to analyze the specificity of Omicron amino acid mutations. Results: It is found that when the proportion of unobserved mutations to observed mutations is 4:15, Omicron still generates a large number of newly emerging mutations. It was found that the overall score for the Omicron family is low, and the overall ranking for the Omicron family is low. Conclusion: Mutations in the Omicron lineage are different from amino acid mutations in other lineages. The findings of this paper deepen the understanding of the spatial distribution of spike protein amino acid mutations and overall trends of newly emerging mutations corresponding to different variants of concern. This also provides insights into simulating the evolution of the Omicron lineage.\",\"PeriodicalId\":10801,\"journal\":{\"name\":\"Current Bioinformatics\",\"volume\":\"63 1\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-04-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Bioinformatics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.2174/0115748936291075240409080924\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.2174/0115748936291075240409080924","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Validating the Distinctiveness of the Omicron Lineage within the SARSCov-2 based on Protein Language Models
Introduction: Variants of concern were identified in severe acute respiratory syndrome coronavirus 2, namely Alpha, Beta, Gamma, Delta, and Omicron. This study explores the mutations of the Omicron lineage and its differences from other lineages through a protein language model. Methods: By inputting the severe acute respiratory syndrome coronavirus 2 wild-type sequence into the protein language model evolving pre-trained models-1v, this study obtained the score for each position mutating to other amino acids and calculated the overall trend of a new variant of concern mutation scores. objective: Analyze the differences in the number of Omicron amino acid mutations compared to the other four VOC mutations using statistical methods, and use the protein language model esm-1v to analyze the specificity of Omicron amino acid mutations. Results: It is found that when the proportion of unobserved mutations to observed mutations is 4:15, Omicron still generates a large number of newly emerging mutations. It was found that the overall score for the Omicron family is low, and the overall ranking for the Omicron family is low. Conclusion: Mutations in the Omicron lineage are different from amino acid mutations in other lineages. The findings of this paper deepen the understanding of the spatial distribution of spike protein amino acid mutations and overall trends of newly emerging mutations corresponding to different variants of concern. This also provides insights into simulating the evolution of the Omicron lineage.
期刊介绍:
Current Bioinformatics aims to publish all the latest and outstanding developments in bioinformatics. Each issue contains a series of timely, in-depth/mini-reviews, research papers and guest edited thematic issues written by leaders in the field, covering a wide range of the integration of biology with computer and information science.
The journal focuses on advances in computational molecular/structural biology, encompassing areas such as computing in biomedicine and genomics, computational proteomics and systems biology, and metabolic pathway engineering. Developments in these fields have direct implications on key issues related to health care, medicine, genetic disorders, development of agricultural products, renewable energy, environmental protection, etc.