Higgs Richard E, Butler Jon P, Han Bomie, Knierman Michael D
Global Discovery and Development Statistics, Lilly Research Laboratories, Indianapolis, IN 46285, USA ; Lilly Corporate Center, DC 0720, Indianapolis, IN 46285, USA.
Int J Proteomics. 2013;2013:674282. doi: 10.1155/2013/674282. Epub 2013 Apr 23.
Recent improvements in the mass accuracy and resolution of mass spectrometers have led to renewed interest in label-free quantification using data from the primary mass spectrum (MS1) acquired from data-dependent proteomics experiments. The capacity for higher specificity quantification of peptides from samples enriched for proteins of biological interest offers distinct advantages for hypothesis generating experiments relative to immunoassay detection methods or prespecified peptide ions measured by multiple reaction monitoring (MRM) approaches. Here we describe an evaluation of different methods to post-process peptide level quantification information to support protein level inference. We characterize the methods by examining their ability to recover a known dilution of a standard protein in background matrices of varying complexity. Additionally, the MS1 quantification results are compared to a standard, targeted, MRM approach on the same samples under equivalent instrument conditions. We show the existence of multiple peptides with MS1 quantification sensitivity similar to the best MRM peptides for each of the background matrices studied. Based on these results we provide recommendations on preferred approaches to leveraging quantitative measurements of multiple peptides to improve protein level inference.
质谱仪在质量精度和分辨率方面的最新进展,使得人们重新关注利用数据依赖型蛋白质组学实验获得的一级质谱(MS1)数据进行无标记定量分析。相对于免疫分析检测方法或通过多反应监测(MRM)方法测量的预先指定的肽离子,从富含生物感兴趣蛋白质的样品中对肽进行更高特异性定量的能力,为假设生成实验提供了明显优势。在此,我们描述了对不同方法进行后处理肽水平定量信息以支持蛋白质水平推断的评估。我们通过检查它们在不同复杂程度的背景基质中恢复已知稀释度标准蛋白质的能力来表征这些方法。此外,在等效仪器条件下,将相同样品上的MS1定量结果与标准的、靶向的MRM方法进行比较。我们表明,在所研究的每种背景基质中,存在多种具有与最佳MRM肽相似的MS1定量灵敏度的肽。基于这些结果,我们就利用多种肽的定量测量来改善蛋白质水平推断的首选方法提供了建议。