基于深度学习的 MS2 特征检测,用于与数据无关的射枪蛋白质组学。

Jonathan He, Olivia Liu, Xuan Guo
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引用次数: 0

摘要

液相色谱-质谱分析中肽段鉴定的准确性对于蛋白质方面的信息至关重要,有助于生物标记物的发现和复杂蛋白质组的分析。在串联质谱中检测肽片段离子仍然是一项挑战,因为目前的工具并不是针对 MS2 数据中发现的低丰度、低峰值肽片段而开发或测试的。特征检测是液相色谱-质谱分析流水线中一个关键的预处理步骤,它通过肽段的质量电荷比、保留时间和强度对肽段进行量化,但由于肽段的重叠性以及弱信号往往无法与噪声区分开来,因此对僵化的数学结构和启发式方法产生了依赖,这一点尤其具有挑战性。在本研究中,我们开发了一种基于深度学习的模型,该模型具有创新的滑动窗口过程,可对定量 MS/MS 数据进行高分辨率处理,从而进行 MS2 特征检测。实验结果表明,与现有的特征检测工具相比,我们的模型能得出更准确的数值和识别结果,而且量化特征的真阳性率也很高。因此,我们认为我们的模型体现了深度学习技术在计算蛋白质组学方面的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep Learning Based MS2 Feature Detection for Data-Independent Shotgun Proteomics.

Accuracy of peptide identification in LC-MS analysis is crucial for information regarding the aspects of proteins that aid in biomarker discovery and the profiling of complex proteomes. The detection of peptide fragment ions in tandem mass spectrometry is still challenging given that current tools were not created or tested for the low-abundance, low-peak fragments of peptides found in MS2 data. Feature detection, a crucial pre-processing step in the LC-MS analysis pipeline that quantifies peptides by their mass-to-charge ratio, retention time, and intensity, is particularly challenging due to the overlapping nature of peptides and weak signals that are often indistinguishable from noises, thus creating a reliance on rigid mathematical structures and heuristics. In this study, we developed a deep-learning-based model with an innovative sliding window process that enables high-resolution processing of quantitative MS/MS data to conduct MS2 feature detection. Experimental results show that our model can produce more accurate values and identifications than existing feature detection tools, as well as a high rate of true positive features quantified. Therefore, we believe that our model illustrates the advantages of deep learning techniques applied towards computational proteomics.

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