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预测小分子的过氧化物酶体增殖物激活受体γ活性:一种由Enalos云平台驱动的协同共识模型和深度学习结合亲和力方法

Predicting peroxisome proliferator-activated receptor gamma potency of small molecules: a synergistic consensus model and deep learning binding affinity approach powered by Enalos Cloud Platform.

作者信息

Antoniou Maria, Papavasileiou Konstantinos D, Tsoumanis Antreas, Melagraki Georgia, Afantitis Antreas

机构信息

Department of ChemoInformatics, NovaMechanics Ltd, 1070, Nicosia, Cyprus.

Computation-Based Science and Technology Research Centre, The Cyprus Institute, 2121, Nicosia, Cyprus.

出版信息

Mol Divers. 2025 Jun 14. doi: 10.1007/s11030-025-11230-6.

Abstract

Peroxisome proliferator-activated receptor gamma (PPARγ) antagonists play a critical role in regulating glucose and lipid metabolism, making them promising candidates for antidiabetic therapies. To support the ongoing search of such compounds, this study introduces two advanced in silico models for predicting the binding affinity and biological activity of small molecules targeting PPARγ. A neural network was developed to classify compounds as strong or weak binders based on molecular docking scores. Additionally, a consensus model combining Random Forest, Support Vector Machine, and k-Nearest Neighbours algorithms was implemented to predict the antagonistic activity of small molecules. Both models were rigorously validated according to the Organisation for Economic Co-operation and Development (OECD) guidelines, to ensure generalisability and sufficient efficiency in detecting the minority class (active antagonists). Mechanistic insights into how key molecular descriptors influence PPARγ activity were discussed in a posteriori interpretation. A case study involving 34 prioritised per- and polyfluoroalkyl substances (PFAS) were screened with the developed workflows to demonstrate their practical application. The models, integrated into user-friendly web applications via the Enalos Cloud Platform, enable accessible and efficient virtual screening, supporting the discovery of PPARγ modulators.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)拮抗剂在调节葡萄糖和脂质代谢中起关键作用,使其成为抗糖尿病治疗的有前景的候选药物。为了支持对这类化合物的持续研究,本研究引入了两种先进的计算机模拟模型,用于预测靶向PPARγ的小分子的结合亲和力和生物活性。开发了一种神经网络,根据分子对接分数将化合物分类为强结合剂或弱结合剂。此外,实施了一种结合随机森林、支持向量机和k近邻算法的共识模型,以预测小分子的拮抗活性。根据经济合作与发展组织(OECD)的指导方针,对这两种模型进行了严格验证,以确保在检测少数类(活性拮抗剂)时具有通用性和足够的效率。在事后解释中讨论了关键分子描述符如何影响PPARγ活性的机制见解。通过开发的工作流程对涉及34种优先全氟和多氟烷基物质(PFAS)的案例研究进行了筛选,以证明其实际应用。这些模型通过Enalos云平台集成到用户友好的网络应用程序中,实现了便捷高效的虚拟筛选,支持PPARγ调节剂的发现。

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