• 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

多任务深度神经网络在 Ames 致突变性预测中的应用。

Multitask Deep Neural Networks for Ames Mutagenicity Prediction.

机构信息

ISISTAN (CONICET - UNCPBA) Campus Universitario - Paraje Arroyo Seco, 7000, Tandil, Argentina.

Institute for Computer Science and Engineering, UNS-CONICET, 8000, Bahía Blanca, Argentina.

出版信息

J Chem Inf Model. 2022 Dec 26;62(24):6342-6351. doi: 10.1021/acs.jcim.2c00532. Epub 2022 Sep 6.

DOI:10.1021/acs.jcim.2c00532
PMID:36066065
Abstract

The Ames mutagenicity test constitutes the most frequently used assay to estimate the mutagenic potential of drug candidates. While this test employs experimental results using various strains of , the vast majority of the published in silico models for predicting mutagenicity do not take into account the test results of the individual experiments conducted for each strain. Instead, such QSAR models are generally trained employing overall labels (i.e., and ). Recently, neural-based models combined with multitask learning strategies have yielded interesting results in different domains, given their capabilities to model multitarget functions. In this scenario, we propose a novel neural-based QSAR model to predict mutagenicity that leverages experimental results from different strains involved in the Ames test by means of a multitask learning approach. To the best of our knowledge, the modeling strategy hereby proposed has not been applied to model Ames mutagenicity previously. The results yielded by our model surpass those obtained by single-task modeling strategies, such as models that predict the overall Ames label or ensemble models built from individual strains. For reproducibility and accessibility purposes, all source code and datasets used in our experiments are publicly available.

摘要

Ames 致突变性试验是用于评估药物候选物致突变潜力的最常用的检测方法。虽然该试验使用了各种菌株的实验结果,但绝大多数用于预测致突变性的计算毒理学模型并未考虑到为每个菌株进行的个别实验的测试结果。相反,这些 QSAR 模型通常使用整体标签(即“肯定”和“否定”)进行训练。最近,基于神经网络的模型结合多任务学习策略,由于其能够模拟多目标功能,在不同领域取得了有趣的结果。在这种情况下,我们提出了一种新的基于神经网络的 QSAR 模型,通过多任务学习方法利用 Ames 试验中涉及的不同菌株的实验结果来预测致突变性。据我们所知,目前还没有提出的建模策略用于模拟 Ames 致突变性。我们的模型产生的结果优于单任务建模策略的结果,例如预测整体 Ames 标签的模型或由个别菌株构建的集成模型。为了可重复性和可访问性,我们实验中使用的所有源代码和数据集都可以公开获取。

相似文献

1
Multitask Deep Neural Networks for Ames Mutagenicity Prediction.多任务深度神经网络在 Ames 致突变性预测中的应用。
J Chem Inf Model. 2022 Dec 26;62(24):6342-6351. doi: 10.1021/acs.jcim.2c00532. Epub 2022 Sep 6.
2
Mechanistic Task Groupings Enhance Multitask Deep Learning of Strain-Specific Ames Mutagenicity.机制任务分组增强了针对特定菌株的 Ames 致突变性的多任务深度学习。
Chem Res Toxicol. 2023 Aug 21;36(8):1248-1254. doi: 10.1021/acs.chemrestox.2c00385. Epub 2023 Jul 21.
3
Multiple Instance Learning Improves Ames Mutagenicity Prediction for Problematic Molecular Species.多实例学习提高对问题分子物种的 Ames 致突变性预测。
Chem Res Toxicol. 2023 Aug 21;36(8):1227-1237. doi: 10.1021/acs.chemrestox.2c00372. Epub 2023 Jul 21.
4
Improvement of quantitative structure-activity relationship (QSAR) tools for predicting Ames mutagenicity: outcomes of the Ames/QSAR International Challenge Project.用于预测埃姆斯致突变性的定量构效关系(QSAR)工具的改进:埃姆斯/QSAR国际挑战赛项目的成果
Mutagenesis. 2019 Mar 6;34(1):3-16. doi: 10.1093/mutage/gey031.
5
Comparative evaluation of 11 in silico models for the prediction of small molecule mutagenicity: role of steric hindrance and electron-withdrawing groups.用于预测小分子致突变性的11种计算机模拟模型的比较评估:空间位阻和吸电子基团的作用
Toxicol Mech Methods. 2017 Jan;27(1):24-35. doi: 10.1080/15376516.2016.1174761. Epub 2016 Nov 4.
6
DeepAmes: A deep learning-powered Ames test predictive model with potential for regulatory application.深度艾姆斯试验:一种由深度学习驱动的具有监管应用潜力的艾姆斯试验预测模型。
Regul Toxicol Pharmacol. 2023 Oct;144:105486. doi: 10.1016/j.yrtph.2023.105486. Epub 2023 Aug 25.
7
AMPred-CNN: Ames mutagenicity prediction model based on convolutional neural networks.AMPred-CNN:基于卷积神经网络的 Ames 诱变预测模型。
Comput Biol Med. 2024 Jun;176:108560. doi: 10.1016/j.compbiomed.2024.108560. Epub 2024 May 8.
8
Strategy proposal using QSAR models to approach mutagenicity assessment of non intentionally added substances in recycled plastic resins.利用定量构效关系模型策略建议评估再生塑料树脂中不可避免添加物质的致突变性。
Food Chem Toxicol. 2024 May;187:114597. doi: 10.1016/j.fct.2024.114597. Epub 2024 Mar 15.
9
Machine learning - Predicting Ames mutagenicity of small molecules.机器学习——预测小分子的艾姆斯致突变性。
J Mol Graph Model. 2021 Dec;109:108011. doi: 10.1016/j.jmgm.2021.108011. Epub 2021 Sep 5.
10
Predicting Ames Mutagenicity Using Conformal Prediction in the Ames/QSAR International Challenge Project.在艾姆斯/定量构效关系国际挑战赛项目中使用共形预测法预测艾姆斯诱变性
Mutagenesis. 2019 Mar 6;34(1):33-40. doi: 10.1093/mutage/gey038.

引用本文的文献

1
Recent advances in AI-based toxicity prediction for drug discovery.基于人工智能的药物发现毒性预测的最新进展。
Front Chem. 2025 Jul 8;13:1632046. doi: 10.3389/fchem.2025.1632046. eCollection 2025.
2
AMPred-MFG: Investigating the Mutagenicity of Compounds Using Motif-Based Graph Combined with Molecular Fingerprints and Graph Attention Mechanism.AMPred-MFG:利用基于基序的图结合分子指纹和图注意力机制研究化合物的致突变性。
Interdiscip Sci. 2025 Jul 16. doi: 10.1007/s12539-025-00742-2.
3
Comparison of new secondgeneration H1 receptor blockers with some molecules; a study involving DFT, molecular docking, ADMET, biological target and activity.
新型第二代H1受体阻滞剂与某些分子的比较;一项涉及密度泛函理论(DFT)、分子对接、药物代谢动力学(ADMET)、生物靶点及活性的研究。
BMC Chem. 2025 Jan 4;19(1):4. doi: 10.1186/s13065-024-01371-4.
4
Deep active learning with high structural discriminability for molecular mutagenicity prediction.基于高结构可区分性的深度主动学习在分子突变预测中的应用。
Commun Biol. 2024 Aug 31;7(1):1071. doi: 10.1038/s42003-024-06758-6.
5
A novel multitask learning algorithm for tasks with distinct chemical space: zebrafish toxicity prediction as an example.一种用于具有不同化学空间任务的新型多任务学习算法:以斑马鱼毒性预测为例。
J Cheminform. 2024 Aug 2;16(1):91. doi: 10.1186/s13321-024-00891-4.