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Comparative Analyses of Data Independent Acquisition Mass Spectrometric Approaches: DIA WiSIM‐DIA and Untargeted DIA

机译:数据独立采集质谱方法的比较分析:DIAWiSIM‐DIA和非目标DIA

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摘要

Data‐independent acquisition (DIA) is an emerging technology for quantitative proteomics. Current DIA focusses on the identification and quantitation of fragment ions that are generated from multiple peptides contained in the same selection window of several to tens of m/z. An alternative approach is WiSIM‐DIA, which combines conventional DIA with wide‐SIM (wide selected‐ion monitoring) windows to partition the precursor m/z space to produce high‐quality precursor ion chromatograms. However, WiSIM‐DIA has been underexplored; it remains unclear if it is a viable alternative to DIA. We demonstrate that WiSIM‐DIA quantified more than 24 000 unique peptides over five orders of magnitude in a single 2 h analysis of a neuronal synapse‐enriched fraction, compared to 31 000 in DIA. There is a strong correlation between abundance values of peptides quantified in both the DIA and WiSIM‐DIA datasets. Interestingly, the S/N ratio of these peptides is not correlated. We further show that peptide identification directly from DIA spectra identified >2000 proteins, which included unique peptides not found in spectral libraries generated by DDA.
机译:数据独立采集(DIA)是一种用于定量蛋白质组学的新兴技术。当前的DIA专注于鉴定和定量碎片离子,这些碎片离子是由同一选择窗口中包含的几十至数十m / z的多种肽产生的。另一种方法是WiSIM-DIA,它将传统的DIA与宽SIM(宽选择离子监测)窗口结合在一起,以划分前体m / z空间,以产生高质量的前体离子色谱图。但是,WiSIM‐DIA尚未得到充分开发。尚不清楚它是否可以替代DIA。我们证明WiSIM‐DIA在神经元突触富集部分的单次2小时分析中,在五个数量级上定量了超过24万种独特肽,而DIA中为31,000种。在DIA和WiSIM-DIA数据集中量化的肽丰度值之间有很强的相关性。有趣的是,这些肽的信噪比不相关。我们进一步表明,直接从DIA光谱中鉴定出的肽段可鉴定> 2000种蛋白质,其中包括在DDA生成的光谱库中未发现的独特肽段。

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