CAPRI第55轮抗体-抗原靶点的大规模采样策略

IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nessim Raouraoua, Marc F Lensink, Guillaume Brysbaert
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引用次数: 0

摘要

大规模采样与AlphaFold2提高蛋白质蛋白质复合物的预测。这在AFsample工具的最后一轮CASP15-CAPRI盲预测中得到了证明。然而,包括抗体-抗原结合在内的更困难的目标仍然具有挑战性。CAPRI第55轮包括三个抗体抗原靶点和一个异源三聚体。我们使用基于alphafold2的MassiveFold,运行6个预测池,每个预测池都有自己的一组参数,每个目标总共产生6000多个预测。我们在这里表明,大规模抽样分类地产生可接受的高质量预测,但很明显,AlphaFold2置信度评分不能用于识别集合中的最佳模型。我们还表明,与之前使用AFsample对CASP15-CAPRI所做的相反,在不激活dropout的情况下增加采样为第55轮的大多数目标提供了最佳模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Massive Sampling Strategy for Antibody-Antigen Targets in CAPRI Round 55 With MassiveFold.

Massive sampling with AlphaFold2 improves protein-protein complex predictions. This has been shown during the last CASP15-CAPRI blind prediction round by the AFsample tool. However, more difficult targets including antibody-antigen binding remain challenging. CAPRI Round 55 consisted of three antibody-antigen targets and one heterotrimer. We used our AlphaFold2-based MassiveFold, running 6 prediction pools, each with their own set of parameters, to produce in total more than 6000 predictions per target. We show here that massive sampling categorically produces acceptable to high quality predictions, however it is clear that the AlphaFold2 confidence score cannot be used to identify the best models in the set. We also show that, contrary to what was done before for CASP15-CAPRI with AFsample, increasing the sampling without activating the dropout provides the best models for most of the targets of Round 55.

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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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