Department of Chemistry, and Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Department of Computer Science, and Institute of Modern Languages and Linguistics, Fudan University, Shanghai, China.
Nat Commun. 2023 Apr 20;14(1):2269. doi: 10.1038/s41467-023-38035-1.
Protein phosphorylation is a post-translational modification crucial for many cellular processes and protein functions. Accurate identification and quantification of protein phosphosites at the proteome-wide level are challenging, not least because efficient tools for protein phosphosite false localization rate (FLR) control are lacking. Here, we propose DeepFLR, a deep learning-based framework for controlling the FLR in phosphoproteomics. DeepFLR includes a phosphopeptide tandem mass spectrum (MS/MS) prediction module based on deep learning and an FLR assessment module based on a target-decoy approach. DeepFLR improves the accuracy of phosphopeptide MS/MS prediction compared to existing tools. Furthermore, DeepFLR estimates FLR accurately for both synthetic and biological datasets, and localizes more phosphosites than probability-based methods. DeepFLR is compatible with data from different organisms, instruments types, and both data-dependent and data-independent acquisition approaches, thus enabling FLR estimation for a broad range of phosphoproteomics experiments.
蛋白质磷酸化是许多细胞过程和蛋白质功能的关键翻译后修饰。在蛋白质组范围内准确识别和定量磷酸化位点具有挑战性,尤其是因为缺乏有效的蛋白质磷酸化位点错误定位率(FLR)控制工具。在这里,我们提出了 DeepFLR,这是一种基于深度学习的磷酸蛋白质组学中控制 FLR 的框架。DeepFLR 包括基于深度学习的磷酸肽串联质谱 (MS/MS) 预测模块和基于靶标-诱饵方法的 FLR 评估模块。与现有工具相比,DeepFLR 提高了磷酸肽 MS/MS 预测的准确性。此外,DeepFLR 可以准确估计合成和生物数据集的 FLR,并且比基于概率的方法定位更多的磷酸化位点。DeepFLR 与来自不同生物体、仪器类型以及数据依赖和独立采集方法的数据兼容,从而能够为广泛的磷酸蛋白质组学实验进行 FLR 估计。