{"title":"利用 GCN 和计算模型揭示以 L-FABP 为靶标的全氟辛烷磺酸的肝毒性机制","authors":"Lucas Jividen, Tibo Duran, Xi-Zhi Niu, Jun Bai","doi":"arxiv-2409.10370","DOIUrl":null,"url":null,"abstract":"Per- and polyfluoroalkyl substances (PFAS) are persistent environmental\npollutants with known toxicity and bioaccumulation issues. Their widespread\nindustrial use and resistance to degradation have led to global environmental\ncontamination and significant health concerns. While a minority of PFAS have\nbeen extensively studied, the toxicity of many PFAS remains poorly understood\ndue to limited direct toxicological data. This study advances the predictive\nmodeling of PFAS toxicity by combining semi-supervised graph convolutional\nnetworks (GCNs) with molecular descriptors and fingerprints. We propose a novel\napproach to enhance the prediction of PFAS binding affinities by isolating\nmolecular fingerprints to construct graphs where then descriptors are set as\nthe node features. This approach specifically captures the structural,\nphysicochemical, and topological features of PFAS without overfitting due to an\nabundance of features. Unsupervised clustering then identifies representative\ncompounds for detailed binding studies. Our results provide a more accurate\nability to estimate PFAS hepatotoxicity to provide guidance in chemical\ndiscovery of new PFAS and the development of new safety regulations.","PeriodicalId":501266,"journal":{"name":"arXiv - QuanBio - Quantitative Methods","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Uncovering the Mechanism of Hepatotoxiciy of PFAS Targeting L-FABP Using GCN and Computational Modeling\",\"authors\":\"Lucas Jividen, Tibo Duran, Xi-Zhi Niu, Jun Bai\",\"doi\":\"arxiv-2409.10370\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Per- and polyfluoroalkyl substances (PFAS) are persistent environmental\\npollutants with known toxicity and bioaccumulation issues. Their widespread\\nindustrial use and resistance to degradation have led to global environmental\\ncontamination and significant health concerns. While a minority of PFAS have\\nbeen extensively studied, the toxicity of many PFAS remains poorly understood\\ndue to limited direct toxicological data. This study advances the predictive\\nmodeling of PFAS toxicity by combining semi-supervised graph convolutional\\nnetworks (GCNs) with molecular descriptors and fingerprints. We propose a novel\\napproach to enhance the prediction of PFAS binding affinities by isolating\\nmolecular fingerprints to construct graphs where then descriptors are set as\\nthe node features. This approach specifically captures the structural,\\nphysicochemical, and topological features of PFAS without overfitting due to an\\nabundance of features. Unsupervised clustering then identifies representative\\ncompounds for detailed binding studies. Our results provide a more accurate\\nability to estimate PFAS hepatotoxicity to provide guidance in chemical\\ndiscovery of new PFAS and the development of new safety regulations.\",\"PeriodicalId\":501266,\"journal\":{\"name\":\"arXiv - QuanBio - Quantitative Methods\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Quantitative Methods\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2409.10370\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Quantitative Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.10370","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Uncovering the Mechanism of Hepatotoxiciy of PFAS Targeting L-FABP Using GCN and Computational Modeling
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental
pollutants with known toxicity and bioaccumulation issues. Their widespread
industrial use and resistance to degradation have led to global environmental
contamination and significant health concerns. While a minority of PFAS have
been extensively studied, the toxicity of many PFAS remains poorly understood
due to limited direct toxicological data. This study advances the predictive
modeling of PFAS toxicity by combining semi-supervised graph convolutional
networks (GCNs) with molecular descriptors and fingerprints. We propose a novel
approach to enhance the prediction of PFAS binding affinities by isolating
molecular fingerprints to construct graphs where then descriptors are set as
the node features. This approach specifically captures the structural,
physicochemical, and topological features of PFAS without overfitting due to an
abundance of features. Unsupervised clustering then identifies representative
compounds for detailed binding studies. Our results provide a more accurate
ability to estimate PFAS hepatotoxicity to provide guidance in chemical
discovery of new PFAS and the development of new safety regulations.