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从蛋白质组学原始数据中提取数据:使用大型 Orbitrap 数据集评估九种串联 MS 工具。

Data extraction from proteomics raw data: an evaluation of nine tandem MS tools using a large Orbitrap data set.

机构信息

Centro de Regulación Genòmica (CRG), C/Dr. Aiguader 88, 08003 Barcelona, Spain.

出版信息

J Proteomics. 2012 Sep 18;75(17):5293-303. doi: 10.1016/j.jprot.2012.06.012. Epub 2012 Jun 20.

Abstract

In shot-gun proteomics raw tandem MS data are processed with extraction tools to produce condensed peak lists that can be uploaded to database search engines. Many extraction tools are available but to our knowledge, a systematic comparison of such tools has not yet been carried out. Using raw data containing more than 400,000 tandem MS spectra acquired using an Orbitrap Velos we compared 9 tandem MS extraction tools, freely available as well as commercial. We compared the tools with respect to number of extracted MS/MS events, fragment ion information, number of matches, precursor mass accuracies and agreement in-between tools. Processing a primary data set with 9 different tandem MS extraction tools resulted in a low overlap of identified peptides. The tools differ by assigned charge states of precursors, precursor and fragment ion masses, and we show that peptides identified very confidently using one extraction tool might not be matched when using another tool. We also found a bias towards peptides of lower charge state when extracting fragment ion data from higher resolution raw data without deconvolution. Collecting and comparing the extracted data from the same raw data allow adjusting parameters and expectations and selecting the right tool for extraction of tandem MS data.

摘要

在 shotgun 蛋白质组学中,原始串联 MS 数据经过提取工具进行处理,生成可上传到数据库搜索引擎的浓缩峰列表。有许多提取工具可用,但据我们所知,尚未对这些工具进行系统比较。使用包含超过 400,000 个使用 Orbitrap Velos 获得的串联 MS 谱的原始数据,我们比较了 9 种免费和商业的串联 MS 提取工具。我们比较了这些工具在提取的 MS/MS 事件数量、片段离子信息、匹配数量、前体质量精度以及工具之间的一致性方面的性能。使用 9 种不同的串联 MS 提取工具处理一个原始数据集导致鉴定的肽的重叠率很低。这些工具在前体、前体和片段离子质量的分配电荷状态、分配电荷状态、前体和片段离子质量等方面存在差异,我们表明,使用一种提取工具非常有信心鉴定的肽在使用另一种工具时可能无法匹配。我们还发现,在不对原始数据进行解卷积的情况下,从更高分辨率的原始数据中提取片段离子数据时,存在偏向于较低电荷状态的肽的趋势。从相同的原始数据中收集和比较提取的数据可以调整参数和预期,并选择正确的工具来提取串联 MS 数据。

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