IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Victor Reys, Marco Giulini, Vlad Cojocaru, Anna Engel, Xiaotong Xu, Jorge Roel-Touris, Cunliang Geng, Francesco Ambrosetti, Brian Jiménez-García, Zuzana Jandova, Panagiotis I Koukos, Charlotte van Noort, João M C Teixeira, Siri C van Keulen, Manon Réau, Rodrigo V Honorato, Alexandre M J J Bonvin
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引用次数: 0

摘要

HADDOCK团队作为服务器、人工预测器和记分员参加了CAPRI第47-55轮比赛。在这些CAPRI回合中,我们使用了大量的计算策略来预测蛋白质复合物的结构。在包含24个接口的10个目标中,我们为人类类别的3个目标和服务器类别的1个目标实现了可接受或更好的模型。我们在评分挑战中的表现稍好一些,我们的简单评分协议是唯一能够为目标234识别可接受模型的协议。这一结果突出了简单的、完全基于物理的HADDOCK评分功能的稳健性,特别是当应用于高度灵活的抗体-抗原复合物时。受结构生物学机器学习的重大进展和Alphafold2公开发布后我们成功率的显着提高的启发,我们确定将经典方法(如HADDOCK)与人工智能驱动的结构预测方法相结合,作为提高模型生成和评分准确性的关键策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrative Modeling in the Age of Machine Learning: A Summary of HADDOCK Strategies in CAPRI Rounds 47-55.

The HADDOCK team participated in CAPRI rounds 47-55 as server, manual predictor, and scorers. Throughout these CAPRI rounds, we used a plethora of computational strategies to predict the structure of protein complexes. Of the 10 targets comprising 24 interfaces, we achieved acceptable or better models for 3 targets in the human category and 1 in the server category. Our performance in the scoring challenge was slightly better, with our simple scoring protocol being the only one capable of identifying an acceptable model for Target 234. This result highlights the robustness of the simple, fully physics-based HADDOCK scoring function, especially when applied to highly flexible antibody-antigen complexes. Inspired by the significant advances in machine learning for structural biology and the dramatic improvement in our success rates after the public release of Alphafold2, we identify the integration of classical approaches like HADDOCK with AI-driven structure prediction methods as a key strategy for improving the accuracy of model generation and scoring.

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来源期刊
Proteins-Structure Function and Bioinformatics
Proteins-Structure Function and Bioinformatics 生物-生化与分子生物学
CiteScore
5.90
自引率
3.40%
发文量
172
审稿时长
3 months
期刊介绍: PROTEINS : Structure, Function, and Bioinformatics publishes original reports of significant experimental and analytic research in all areas of protein research: structure, function, computation, genetics, and design. The journal encourages reports that present new experimental or computational approaches for interpreting and understanding data from biophysical chemistry, structural studies of proteins and macromolecular assemblies, alterations of protein structure and function engineered through techniques of molecular biology and genetics, functional analyses under physiologic conditions, as well as the interactions of proteins with receptors, nucleic acids, or other specific ligands or substrates. Research in protein and peptide biochemistry directed toward synthesizing or characterizing molecules that simulate aspects of the activity of proteins, or that act as inhibitors of protein function, is also within the scope of PROTEINS. In addition to full-length reports, short communications (usually not more than 4 printed pages) and prediction reports are welcome. Reviews are typically by invitation; authors are encouraged to submit proposed topics for consideration.
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