arXiv:2507.07862cs.LGq-bio.QM2025-07被引 3

AI模型可预测新病原体抗生素效力并生成全新分子。

Predicting and generating antibiotics against future pathogens with ApexOracle

  • 融合基因组与文献数据,构建病原体特异性表示
  • 对未知病原体预测准确率超越现有方法
  • 能生成全新有效分子,适合抗药性研究

抗菌素耐药性(AMR)正加速蔓延,超过当前抗生素研发速度。现有方法难以快速识别对新病原体或耐药菌株有效的化合物。本文提出ApexOracle,一种人工智能模型,既能预测现有化合物的抗菌活性,又能针对从未见过的病原体设计全新分子。该模型结合离散扩散语言模型提取分子特征,以及基于基因组和文献的双嵌入框架,融入病原体特异性上下文。在多种细菌物种和化学类型中,ApexOracle在活性预测上持续优于当前最优方法,并在缺乏抗菌数据的新病原体上表现出可靠泛化能力。其统一的表征-生成架构可实现“自然界不存在”的分子的虚拟生成,对优先威胁病原体具有高预测效力。通过快速预测与定向生成结合,ApexOracle提供了一种可扩展的策略,以应对抗药性挑战并防范未来传染病爆发。

原文摘要 · Abstract (English)

Antimicrobial resistance (AMR) is escalating and outpacing current antibiotic development. Thus, discovering antibiotics effective against emerging pathogens is becoming increasingly critical. However, existing approaches cannot rapidly identify effective molecules against novel pathogens or emerging drug-resistant strains. Here, we introduce ApexOracle, an artificial intelligence (AI) model that both predicts the antibacterial potency of existing compounds and designs de novo molecules active against strains it has never encountered. Departing from models that rely solely on molecular features, ApexOracle incorporates pathogen-specific context through the integration of molecular features captured via a foundational discrete diffusion language model and a dual-embedding framework that combines genomic- and literature-derived strain representations. Across diverse bacterial species and chemical modalities, ApexOracle consistently outperformed state-of-the-art approaches in activity prediction and demonstrated reliable transferability to novel pathogens with little or no antimicrobial data. Its unified representation-generation architecture further enables the in silico creation of "new-to-nature" molecules with high predicted efficacy against priority threats. By pairing rapid activity prediction with targeted molecular generation, ApexOracle offers a scalable strategy for countering AMR and preparing for future infectious-disease outbreaks.

抗生素发现AI制药抗药性

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