工作流程
计算机科学
人工智能
机器学习
甲状腺癌
下调和上调
仿形(计算机编程)
甲状腺
计算生物学
蛋白质降解
吞吐量
细胞
生物信息学
蛋白质-蛋白质相互作用
作者
Mengge Lyu,Pingping Hu,guangmei zhang,Kunpeng Ma,Xuedong Zhang,Pu Liu,Sai Zhang,Xiangqing Li,Rui Sun,Yi Chen,Tiannan Guo
标识
DOI:10.1038/s41467-026-68686-9
摘要
Co-fractionation mass spectrometry (CF-MS) enables large-scale profiling of endogenous protein-protein interactions, yet CF-MS data generation is of low throughput and therefore predictive models are often limited by the scarcity and limited diversity of high-quality training data. To address this, we present ProteoAutoNet, a robotic experimental platform integrated with a computational workflow for high-throughput CF-MS analysis. This workflow increases the throughput of sample processing from protein complex to peptide by about two times. The integrated machine learning model incorporates targeted data augmentation to expand and diversify reliable protein interaction data, thereby improving model robustness. When applied to three thyroid cell lines, the model predicted 25,173 co-eluted proteins with an AUROC of 0.78. This analysis revealed significantly upregulated proteasome and prefoldin complexes in the lung metastatic follicular thyroid carcinoma cell line FTC238 compared with the normal thyroid cell line Nthy-ori 3-1. Notably, we identified a protein interaction between TGM2 and HK1 that was significantly upregulated in the papillary thyroid carcinoma cell line TPC-1. ProteoAutoNet provides an improved framework for investigating protein-protein interactions and uncovering interactions.
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