ANABAG:注释抗体抗原数据集与抗体工程应用的独特功能。

IF 5.3 2区 化学 Q1 CHEMISTRY, MEDICINAL
Ilyas Grandguillaume, Fernando Luís Barroso da Silva, Catherine Etchebest
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引用次数: 0

摘要

抗体-抗原(Ab-Ag)相互作用的分析和预测往往忽略了关键的结构特征,如糖基化和重要的物理化学条件,如pH和盐浓度。此外,该领域缺乏基于结构特性和序列同一性选择复合物的标准化标准。数据集构建中的常见做法依赖于使用序列身份阈值去除冗余,这可能会无意中排除具有共享相同序列的替代绑定模式的复合体。为了实现更精确的Ab-Ag建模和抗体工程,必须将更丰富的结构和物理信息合并到基于物理和机器学习的模型中。为了解决这些限制,我们提出了ANABAG,这是一个新的Ab-Ag复合物数据集,在残基水平上用UniProt序列信息注释,并丰富了广泛的结构和物理化学特征。该数据集允许使用复杂和残留级别上可用的各种描述符灵活地过滤复合物。选定的功能已准备好在机器学习工作流程中使用,而结构文件与抗体设计和对接管道(如Rosetta或Haddock)兼容。完整的数据集可以在Zenodo上获得,网址为https://zenodo.org/records/17065788,所有附带的脚本和使用文档可以通过GitHub访问https://github.com/DSIMB/anabag-handler.git。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ANABAG: Annotated Antibody-Antigen Data Set with Unique Features for Antibody Engineering Applications.

The analysis and prediction of antibody-antigen (Ab-Ag) interactions often overlook critical structural features such as glycosylation and important physicochemical conditions like pH and salt concentration. Additionally, the field lacks standardized criteria for selecting complexes based on structural properties and sequence identity. Common practices in data set construction rely on removing redundancy using sequence identity thresholds, which can inadvertently exclude complexes with alternative binding modes that share identical sequences. To enable more precise Ab-Ag modeling and antibody engineering, it is essential to incorporate richer structural and physical information into both physics-based and machine learning models. To address these limitations, we present ANABAG, a new curated data set of Ab-Ag complexes annotated at the residue level with UniProt sequence information and enriched with a wide range of structural and physicochemical features. The data set allows flexible filtering of complexes using a variety of descriptors available at both the complex and residue levels. Selected features are ready to use in machine learning workflows, while the structural files are compatible with antibody design and docking pipelines like Rosetta or Haddock. The complete data set is available on Zenodo at https://zenodo.org/records/17065788, and all accompanying scripts and usage documentation can be accessed via GitHub at https://github.com/DSIMB/anabag-handler.git.

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来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
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