{"title":"单序列蛋白质- rna复合物结构预测的几何注意激活配对的生物语言模型。","authors":"Rahmatullah Roche, Sumit Tarafder, Debswapna Bhattacharya","doi":"10.1016/j.cels.2025.101400","DOIUrl":null,"url":null,"abstract":"<p><p>Groundbreaking progress has been made in structure prediction of biomolecular assemblies, including the recent breakthrough of AlphaFold 3. However, it remains challenging for AlphaFold 3 and other state-of-the-art deep-learning-based methods to accurately predict protein-RNA complex structures, in part due to the limited availability of evolutionary information related to protein-RNA interactions that are used as inputs to the existing approaches. Here, we introduce ProRNA3D-single, a deep-learning framework for protein-RNA complex structure prediction. Using a geometric attention-enabled pairing of biological language models of protein and RNA, a previously unexplored avenue, ProRNA3D-single predicts interatomic protein-RNA interaction maps, which are then transformed into multi-scale geometric restraints for modeling 3D structures of protein-RNA complexes via geometry optimization. Benchmark tests show that ProRNA3D-single outperforms state-of-the-art methods, including AlphaFold 3, particularly when evolutionary information is limited, and exhibits robustness and performance resilience by attaining state-of-the-art accuracy with only single-sequence input.</p>","PeriodicalId":93929,"journal":{"name":"Cell systems","volume":" ","pages":"101400"},"PeriodicalIF":7.7000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12448100/pdf/","citationCount":"0","resultStr":"{\"title\":\"Single-sequence protein-RNA complex structure prediction by geometric attention-enabled pairing of biological language models.\",\"authors\":\"Rahmatullah Roche, Sumit Tarafder, Debswapna Bhattacharya\",\"doi\":\"10.1016/j.cels.2025.101400\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Groundbreaking progress has been made in structure prediction of biomolecular assemblies, including the recent breakthrough of AlphaFold 3. However, it remains challenging for AlphaFold 3 and other state-of-the-art deep-learning-based methods to accurately predict protein-RNA complex structures, in part due to the limited availability of evolutionary information related to protein-RNA interactions that are used as inputs to the existing approaches. Here, we introduce ProRNA3D-single, a deep-learning framework for protein-RNA complex structure prediction. Using a geometric attention-enabled pairing of biological language models of protein and RNA, a previously unexplored avenue, ProRNA3D-single predicts interatomic protein-RNA interaction maps, which are then transformed into multi-scale geometric restraints for modeling 3D structures of protein-RNA complexes via geometry optimization. Benchmark tests show that ProRNA3D-single outperforms state-of-the-art methods, including AlphaFold 3, particularly when evolutionary information is limited, and exhibits robustness and performance resilience by attaining state-of-the-art accuracy with only single-sequence input.</p>\",\"PeriodicalId\":93929,\"journal\":{\"name\":\"Cell systems\",\"volume\":\" \",\"pages\":\"101400\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12448100/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell systems\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cels.2025.101400\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell systems","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.cels.2025.101400","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Single-sequence protein-RNA complex structure prediction by geometric attention-enabled pairing of biological language models.
Groundbreaking progress has been made in structure prediction of biomolecular assemblies, including the recent breakthrough of AlphaFold 3. However, it remains challenging for AlphaFold 3 and other state-of-the-art deep-learning-based methods to accurately predict protein-RNA complex structures, in part due to the limited availability of evolutionary information related to protein-RNA interactions that are used as inputs to the existing approaches. Here, we introduce ProRNA3D-single, a deep-learning framework for protein-RNA complex structure prediction. Using a geometric attention-enabled pairing of biological language models of protein and RNA, a previously unexplored avenue, ProRNA3D-single predicts interatomic protein-RNA interaction maps, which are then transformed into multi-scale geometric restraints for modeling 3D structures of protein-RNA complexes via geometry optimization. Benchmark tests show that ProRNA3D-single outperforms state-of-the-art methods, including AlphaFold 3, particularly when evolutionary information is limited, and exhibits robustness and performance resilience by attaining state-of-the-art accuracy with only single-sequence input.