使用蛋白质网络和单细胞数据的深度学习将蛋白质表示上下文化。

Michelle M Li, Yepeng Huang, Marissa Sumathipala, Man Qing Liang, Alberto Valdeolivas, Ashwin N Ananthakrishnan, Katherine Liao, Daniel Marbach, Marinka Zitnik
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引用次数: 0

摘要

了解蛋白质功能和发现分子疗法需要破译蛋白质作用的细胞类型以及蛋白质之间的相互作用。然而,对不同生物环境(如组织和细胞类型)中的蛋白质相互作用进行建模,对现有算法来说仍然是一个重大挑战。我们介绍了Pinnacle,这是一种灵活的几何深度学习方法,在上下文化的蛋白质相互作用网络上进行训练,以生成上下文感知的蛋白质表示。利用人类多器官单细胞转录组图谱,Pinnacle提供了394760种蛋白质表示,分布在24个组织和器官的156种细胞类型中。Pinnacle对蛋白质的情境化表示反映了细胞和组织组织组织,Pinnacle的组织表示使组织层级的零样本检索成为可能。预先训练的Pinnacle蛋白表达可用于下游任务:以细胞分辨率增强基于3D结构的蛋白表达(PD-1/PD-L1和B7-1/CTLA-4),并研究药物在细胞环境中的基因组效应。Pinnacle在提名类风湿性关节炎和炎症性肠病的治疗靶点方面优于最先进但无上下文的模型,并且可以确定比无上下文模型更能预测治疗靶点的细胞类型上下文(类风湿性关节病156种细胞类型中有29种;炎性肠病152种细胞类型其中有13种)。Pinnacle是一个基于网络的上下文人工智能模型,它根据其运行的生物上下文动态调整输出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Contextual AI models for single-cell protein biology.

Contextual AI models for single-cell protein biology.

Contextual AI models for single-cell protein biology.

Contextual AI models for single-cell protein biology.

Understanding protein function and developing molecular therapies require deciphering the cell types in which proteins act as well as the interactions between proteins. However, modeling protein interactions across biological contexts remains challenging for existing algorithms. Here, we introduce Pinnacle, a geometric deep learning approach that generates context-aware protein representations. Leveraging a multi-organ single-cell atlas, Pinnacle learns on contextualized protein interaction networks to produce 394,760 protein representations from 156 cell type contexts across 24 tissues. Pinnacle's embedding space reflects cellular and tissue organization, enabling zero-shot retrieval of the tissue hierarchy. Pretrained protein representations can be adapted for downstream tasks: enhancing 3D structure-based representations for resolving immuno-oncological protein interactions, and investigating drugs' effects across cell types. Pinnacle outperforms state-of-the-art models in nominating therapeutic targets for rheumatoid arthritis and inflammatory bowel diseases, and pinpoints cell type contexts with higher predictive capability than context-free models. Pinnacle's ability to adjust its outputs based on the context in which it operates paves way for large-scale context-specific predictions in biology.

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