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EquiRank:使用蛋白质语言模型引导的等变图神经网络改进蛋白质-蛋白质界面质量评估

EquiRank: Improved protein-protein interface quality estimation using protein language-model-informed equivariant graph neural networks.

作者信息

Shuvo Md Hossain, Bhattacharya Debswapna

机构信息

Department of Computer Science, Prairie View A&M University, Prairie View, 77446, TX, USA.

Department of Computer Science, Virginia Tech, Blacksburg, 24061, VA, USA.

出版信息

Comput Struct Biotechnol J. 2024 Dec 30;27:160-170. doi: 10.1016/j.csbj.2024.12.015. eCollection 2025.

DOI:10.1016/j.csbj.2024.12.015
PMID:39850657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11755013/
Abstract

Quality estimation of the predicted interaction interface of protein complex structural models is not only important for complex model evaluation and selection but also useful for protein-protein docking. Despite recent progress fueled by symmetry-aware deep learning architectures and pretrained protein language models (pLMs), existing methods for estimating protein complex quality have yet to fully exploit the collective potentials of these advances for accurate estimation of protein-protein interface. Here we present EquiRank, an improved protein-protein interface quality estimation method by leveraging the strength of a symmetry-aware E(3) equivariant deep graph neural network (EGNN) and integrating pLM embeddings from the pretrained ESM-2 model. Our method estimates the quality of the protein-protein interface through an effective graph-based representation of interacting residue pairs, incorporating a diverse set of features, including ESM-2 embeddings, and then by learning the representation using symmetry-aware EGNNs. Our experimental results demonstrate improved ranking performance on diverse datasets over existing latest protein complex quality estimation methods including the top-performing CASP15 protein complex quality estimation method VoroIF_GNN and the self-assessment module of AlphaFold-Multimer repurposed for protein complex scoring and across different performance evaluation metrics. Additionally, our ablation studies demonstrate the contributions of both pLMs and the equivariant nature of EGNN for improved protein-protein interface quality estimation performance. EquiRank is freely available at https://github.com/mhshuvo1/EquiRank.

摘要

蛋白质复合物结构模型预测的相互作用界面的质量评估不仅对复合物模型的评估和选择很重要,而且对蛋白质-蛋白质对接也很有用。尽管最近在对称感知深度学习架构和预训练蛋白质语言模型(pLMs)的推动下取得了进展,但现有的蛋白质复合物质量评估方法尚未充分利用这些进展的集体潜力来准确估计蛋白质-蛋白质界面。在这里,我们提出了EquiRank,一种改进的蛋白质-蛋白质界面质量评估方法,它利用了对称感知E(3)等变深度图神经网络(EGNN)的优势,并整合了来自预训练的ESM-2模型的pLM嵌入。我们的方法通过对相互作用残基对的有效基于图的表示来估计蛋白质-蛋白质界面的质量,纳入了包括ESM-2嵌入在内的各种特征,然后通过使用对称感知EGNN学习该表示。我们的实验结果表明,在包括顶级的CASP15蛋白质复合物质量评估方法VoroIF_GNN和重新用于蛋白质复合物评分的AlphaFold-Multimer的自我评估模块在内的现有最新蛋白质复合物质量评估方法上,以及在不同的性能评估指标上,在各种数据集上的排名性能都有所提高。此外,我们的消融研究证明了pLMs和EGNN的等变性质对改进蛋白质-蛋白质界面质量评估性能的贡献。EquiRank可在https://github.com/mhshuvo1/EquiRank上免费获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/cab1a2da8da3/gr007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/f33c97094b65/gr006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/cab1a2da8da3/gr007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/047acd0e9e72/gr001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/3020a050182b/gr002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/ef050b52b203/gr003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/03cdfa2d6cc4/gr004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/7ca888b99b45/gr005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/f33c97094b65/gr006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9f/11755013/cab1a2da8da3/gr007.jpg

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本文引用的文献

1
EuDockScore: Euclidean graph neural networks for scoring protein-protein interfaces.EuDockScore:用于打分蛋白质-蛋白质界面的欧几里得图神经网络。
Bioinformatics. 2024 Nov 1;40(11). doi: 10.1093/bioinformatics/btae636.
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Accurate structure prediction of biomolecular interactions with AlphaFold 3.利用 AlphaFold 3 进行生物分子相互作用的精确结构预测。
Nature. 2024 Jun;630(8016):493-500. doi: 10.1038/s41586-024-07487-w. Epub 2024 May 8.
3
EquiPNAS: improved protein-nucleic acid binding site prediction using protein-language-model-informed equivariant deep graph neural networks.
EquiPNAS:利用基于蛋白质语言模型的等变深度图神经网络提高蛋白质-核酸结合位点预测。
Nucleic Acids Res. 2024 Mar 21;52(5):e27. doi: 10.1093/nar/gkae039.
4
Assessing protein model quality based on deep graph coupled networks using protein language model.基于蛋白质语言模型的深度图耦合网络评估蛋白质模型质量。
Brief Bioinform. 2023 Nov 22;25(1). doi: 10.1093/bib/bbad420.
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Integration of pre-trained protein language models into geometric deep learning networks.将预先训练的蛋白质语言模型集成到几何深度学习网络中。
Commun Biol. 2023 Aug 25;6(1):876. doi: 10.1038/s42003-023-05133-1.
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VoroIF-GNN: Voronoi tessellation-derived protein-protein interface assessment using a graph neural network.VoroIF-GNN:使用图神经网络进行基于 Voronoi 剖分的蛋白质-蛋白质界面评估。
Proteins. 2023 Dec;91(12):1879-1888. doi: 10.1002/prot.26554. Epub 2023 Jul 21.
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A gated graph transformer for protein complex structure quality assessment and its performance in CASP15.门控图转换器用于蛋白质复合物结构质量评估及其在 CASP15 中的性能。
Bioinformatics. 2023 Jun 30;39(39 Suppl 1):i308-i317. doi: 10.1093/bioinformatics/btad203.
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GDockScore: a graph-based protein-protein docking scoring function.GDockScore:一种基于图形的蛋白质-蛋白质对接评分函数。
Bioinform Adv. 2023 Jun 12;3(1):vbad072. doi: 10.1093/bioadv/vbad072. eCollection 2023.
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PIQLE: protein-protein interface quality estimation by deep graph learning of multimeric interaction geometries.PIQLE:通过多聚体相互作用几何结构的深度图学习进行蛋白质-蛋白质界面质量评估
Bioinform Adv. 2023 Jun 2;3(1):vbad070. doi: 10.1093/bioadv/vbad070. eCollection 2023.
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Evolutionary-scale prediction of atomic-level protein structure with a language model.用语言模型进行原子级蛋白质结构的进化尺度预测。
Science. 2023 Mar 17;379(6637):1123-1130. doi: 10.1126/science.ade2574. Epub 2023 Mar 16.