管道(软件)
药品
药物发现
铅(地质)
材料科学
计算机科学
纳米技术
药理学
化学
医学
生物
古生物学
生物化学
程序设计语言
作者
Beihong Ji,Matthew Brock,Yuhui Wu,Yuemin Bian,Xibing He,Yue Liu,Yixuan Hao,Haocheng Tang,Junmei Wang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-10-28
卷期号:12 (44): eaei5257-eaei5257
被引量:2
标识
DOI:10.1126/sciadv.aei5257
摘要
We present the Full-Spectrum Generative Lead Discovery (FSGLD), a deep learning-driven pipeline for efficient drug lead identification. FSGLD integrates generative modeling with molecular docking, molecular dynamics simulations, ligand-residue interaction profile, MM-PBSA, thermodynamic integration (TI), and experimental validation to bridge theoretical design and practical application. The core multiscale DRUG-GAN models enable generative model-guided discovery of drug-like and target-specific compounds across three scenarios: (i) generation of random drug-like compounds, (ii) generation of target-specific compounds, and (iii) generation of target-specific compound series featuring shared chemical structures. In our assessment across three pharmacologically distinct target classes, FSGLD demonstrates encouraging performance in identifying target-specific candidate compounds. In addition, a computational protocol for TI calculations was established to reduce computation time by 80 to 90% while maintaining accuracy. By integrating generative models with in silico and in vitro evaluation techniques, FSGLD reduces the cost of identifying previously uncharacterized yet viable lead compounds, offering remarkable benefits to both academic and industry.
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