• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

ParaAntiProt 利用抗体和蛋白质语言模型提供抗体互补决定区(CDR)预测。

ParaAntiProt provides paratope prediction using antibody and protein language models.

机构信息

Department of Computer Engineering, Sharif University of Technology, Tehran, Iran.

出版信息

Sci Rep. 2024 Nov 25;14(1):29141. doi: 10.1038/s41598-024-80940-y.

DOI:10.1038/s41598-024-80940-y
PMID:39587231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11589832/
Abstract

Efficiently predicting the paratope holds immense potential for enhancing antibody design, treating cancers and other serious diseases, and advancing personalized medicine. Although traditional methods are highly accurate, they are often time-consuming, labor-intensive, and reliant on 3D structures, restricting their broader use. On the other hand, machine learning-based methods, besides relying on structural data, entail descriptor computation, consideration of diverse physicochemical properties, and feature engineering. Here, we develop a deep learning-assisted prediction method for paratope identification, relying solely on amino acid sequences and being antigen-agnostic. Built on the ProtTrans architecture, and utilizing pre-trained protein and antibody language models, we extract efficient embeddings for predicting paratope. By incorporating positional encoding for Complementarity Determining Regions, our model gains a deeper structural understanding, achieving remarkable performance with a 0.904 ROC AUC, 0.701 F1-score, and 0.585 MCC on benchmark datasets. In addition to yielding accurate antibody paratope predictions, our method exhibits strong performance in predicting nanobody paratope, achieving a ROC AUC of 0.912 and a PR AUC of 0.665 on the nanobody dataset. Notably, our approach outperforms structure-based prediction methods, boasting a PR AUC of 0.731. Various conducted ablation studies, which elaborate on the impact of each part of the model on the prediction task, show that the improvement in prediction performance by applying CDR positional encoding together with CNNs depends on the specific protein and antibody language models used. These results highlight the potential of our method to advance disease understanding and aid in the discovery of new diagnostics and antibody therapies.

摘要

高效预测抗体的结合表位在增强抗体设计、治疗癌症和其他严重疾病以及推进个性化医疗方面具有巨大潜力。虽然传统方法具有高度准确性,但它们通常耗时、费力且依赖于 3D 结构,限制了其更广泛的应用。另一方面,基于机器学习的方法除了依赖结构数据外,还需要进行描述符计算、考虑多种物理化学性质以及特征工程。在这里,我们开发了一种基于深度学习的抗体结合表位预测方法,该方法仅依赖于氨基酸序列,并且与抗原无关。该方法构建在 ProtTrans 架构之上,利用预先训练的蛋白质和抗体语言模型,为预测结合表位提取有效的嵌入。通过对互补决定区进行位置编码,我们的模型获得了更深入的结构理解,在基准数据集上取得了优异的性能,ROC AUC 为 0.904,F1 得分为 0.701,MCC 得分为 0.585。除了能够准确预测抗体的结合表位外,我们的方法在预测纳米抗体的结合表位方面也表现出了强大的性能,在纳米抗体数据集上的 ROC AUC 为 0.912,PR AUC 为 0.665。值得注意的是,我们的方法在预测性能上优于基于结构的预测方法,其 PR AUC 为 0.731。各种消融研究详细说明了模型的每个部分对预测任务的影响,结果表明,应用 CDR 位置编码与 CNN 一起可以提高预测性能,这取决于所使用的特定蛋白质和抗体语言模型。这些结果突出了我们的方法在推进疾病理解和辅助新诊断和抗体疗法发现方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/737b379c57e7/41598_2024_80940_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/baf94cd09ab0/41598_2024_80940_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/e2f1504b2ae0/41598_2024_80940_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/93f6e1ebc2b5/41598_2024_80940_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/9b02ae3ae1f4/41598_2024_80940_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/18790859cada/41598_2024_80940_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/f9c1b57cdfa0/41598_2024_80940_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/737b379c57e7/41598_2024_80940_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/baf94cd09ab0/41598_2024_80940_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/e2f1504b2ae0/41598_2024_80940_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/93f6e1ebc2b5/41598_2024_80940_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/9b02ae3ae1f4/41598_2024_80940_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/18790859cada/41598_2024_80940_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/f9c1b57cdfa0/41598_2024_80940_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f43/11589832/737b379c57e7/41598_2024_80940_Fig7_HTML.jpg

相似文献

1
ParaAntiProt provides paratope prediction using antibody and protein language models.ParaAntiProt 利用抗体和蛋白质语言模型提供抗体互补决定区(CDR)预测。
Sci Rep. 2024 Nov 25;14(1):29141. doi: 10.1038/s41598-024-80940-y.
2
Accurate prediction of CDR-H3 loop structures of antibodies with deep learning.利用深度学习准确预测抗体的 CDR-H3 环结构。
Elife. 2024 Jun 26;12:RP91512. doi: 10.7554/eLife.91512.
3
NanoBERTa-ASP: predicting nanobody paratope based on a pretrained RoBERTa model.NanoBERTa-ASP:基于预训练的 RoBERTa 模型预测纳米抗体表位。
BMC Bioinformatics. 2024 Mar 21;25(1):122. doi: 10.1186/s12859-024-05750-5.
4
A compact vocabulary of paratope-epitope interactions enables predictability of antibody-antigen binding.一套简洁的互补位-表位相互作用词汇表能够实现抗体-抗原结合的可预测性。
Cell Rep. 2021 Mar 16;34(11):108856. doi: 10.1016/j.celrep.2021.108856.
5
FvFold: A model to predict antibody Fv structure using protein language model with residual network and Rosetta minimization.FvFold:一种使用蛋白质语言模型、残差网络和 Rosetta 最小化预测抗体 Fv 结构的模型。
Comput Biol Med. 2024 Nov;182:109128. doi: 10.1016/j.compbiomed.2024.109128. Epub 2024 Sep 12.
6
ParaSurf: a surface-based deep learning approach for paratope-antigen interaction prediction.ParaSurf:一种基于表面的深度学习方法用于预测互补位-抗原相互作用。
Bioinformatics. 2025 Feb 4;41(2). doi: 10.1093/bioinformatics/btaf062.
7
Accurate prediction of antibody function and structure using bio-inspired antibody language model.使用仿生抗体语言模型准确预测抗体功能和结构。
Brief Bioinform. 2024 May 23;25(4). doi: 10.1093/bib/bbae245.
8
Protein loop structure prediction by community-based deep learning and its application to antibody CDR H3 loop modeling.基于社区的深度学习进行蛋白质环结构预测及其在抗体 CDR H3 环建模中的应用。
PLoS Comput Biol. 2024 Jun 24;20(6):e1012239. doi: 10.1371/journal.pcbi.1012239. eCollection 2024 Jun.
9
Antigen recognition by single-domain antibodies: structural latitudes and constraints.单域抗体对抗原的识别:结构的自由度和约束。
MAbs. 2018 Aug/Sep;10(6):815-826. doi: 10.1080/19420862.2018.1489633. Epub 2018 Aug 15.
10
Physicochemical determinants of antibody-protein interactions.抗体-蛋白质相互作用的理化决定因素。
Adv Protein Chem Struct Biol. 2020;121:85-114. doi: 10.1016/bs.apcsb.2019.08.011. Epub 2019 Nov 19.

引用本文的文献

1
Application of artificial intelligence large language models in drug target discovery.人工智能大语言模型在药物靶点发现中的应用。
Front Pharmacol. 2025 Jul 8;16:1597351. doi: 10.3389/fphar.2025.1597351. eCollection 2025.
2
Nanobodies: From Discovery to AI-Driven Design.纳米抗体:从发现到人工智能驱动的设计
Biology (Basel). 2025 May 14;14(5):547. doi: 10.3390/biology14050547.
3
A comprehensive antigen-antibody complex database unlocking insights into interaction interface.一个全面的抗原-抗体复合物数据库,揭示相互作用界面的见解。
Elife. 2025 May 22;14:RP104934. doi: 10.7554/eLife.104934.
4
DeepInterAware: Deep Interaction Interface-Aware Network for Improving Antigen-Antibody Interaction Prediction from Sequence Data.深度交互感知:用于从序列数据改进抗原-抗体相互作用预测的深度交互界面感知网络
Adv Sci (Weinh). 2025 Apr;12(13):e2412533. doi: 10.1002/advs.202412533. Epub 2025 Feb 11.