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

Lucas Jividen, Tibo Duran, Xi-Zhi Niu, Jun Bai
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摘要

全氟烷基和多氟烷基物质(PFAS)是持久性环境污染物,具有已知的毒性和生物蓄积性问题。它们在工业中的广泛使用和抗降解性导致了全球环境污染和严重的健康问题。虽然已经对少数全氟辛烷磺酸进行了广泛研究,但由于直接毒理学数据有限,人们对许多全氟辛烷磺酸的毒性仍然知之甚少。本研究通过将半监督图卷积网络(GCN)与分子描述符和指纹相结合,推进了全氟辛烷磺酸毒性的预测建模。我们提出了一种新方法,通过分离分子指纹来构建图,然后将描述符设置为节点特征,从而增强对 PFAS 结合亲和力的预测。这种方法特别捕捉到了 PFAS 的结构、物理化学和拓扑特征,而不会因为特征过多而导致过拟合。然后,通过无监督聚类找出具有代表性的化合物,进行详细的结合研究。我们的研究结果可更准确地估计全氟辛烷磺酸的肝毒性,为发现新的全氟辛烷磺酸化学物质和制定新的安全法规提供指导。
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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.
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