用上下文感知模型解析药物扰动下的细胞形态变化原因。
CP-Agent: Context-Aware Multimodal Reasoning for Cellular Morphological Profiling under Chemical Perturbations

- 构建上下文对齐模块CP-CLIP,联合建模图像与实验信息。
- 在药物作用机制识别上达到0.896的F1分数,提升可解释性。
- 适合药物发现中需快速生成假设的研究人员使用。
Cell Painting结合多重荧光染色、高内涵成像和定量分析,生成高维表型读数,用于机制推断、毒性预测及药物-疾病图谱构建。然而现有流程速度慢、成本高且难以解释。当前药物筛选建模多聚焦分子表示学习,忽视实际实验上下文(如细胞系、给药方案等),限制了泛化性和机制分辨率。我们提出CP-Agent,一种具备上下文感知能力的多模态大语言模型,可生成与机制相关、人类可读的细胞形态变化解释。其核心是上下文对齐模块CP-CLIP,联合嵌入高内涵图像与实验元数据,实现稳健的处理与机制区分(最高F1-score达0.896)。通过整合CP-CLIP输出与代理工具调用及推理,CP-Agent生成结构化报告,辅助实验设计与假说优化。该能力有望加速药物发现,推动更可解释、可扩展、上下文敏感的表型筛选,简化药物发现中的假设生成迭代周期。
原文摘要 · Abstract (English)
Cell Painting combines multiplexed fluorescent staining, high-content imaging, and quantitative analysis to generate high-dimensional phenotypic readouts to support diverse downstream tasks such as mechanism-of-action (MoA) inference, toxicity prediction, and construction of drug-disease atlases. However, existing workflows are slow, costly and difficult to interpret. Approaches for drug screening modeling predominantly focus on molecular representation learning, while neglecting actual experimental context (e.g., cell line, dosing schedule, etc.), limiting generalization and MoA resolution. We introduce CP-Agent, an agentic multimodal large language model (MLLM) capable of generating mechanism-relevant, human-interpretable rationales for cell morphological changes under drug perturbations. At its core, CP-Agent leverages a context-aware alignment module, CP-CLIP, that jointly embeds high-content images and experimental metadata to enable robust treatment and MoA discrimination (achieving a maximum F1-score of 0.896). By integrating CP-CLIP outputs with agentic tool usage and reasoning, CP-Agent compiles rationales into a structured report to guide experimental design and hypothesis refinement. These capabilities highlight CP-Agent's potential to accelerate drug discovery by enabling more interpretable, scalable, and context-aware phenotypic screening -- streamlining iterative cycles of hypothesis generation in drug discovery.
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