Department of Chemistry and Biochemistry, Florida International University, Miami, FL, 33199, USA.
Biological Sciences Division and Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
J Am Soc Mass Spectrom. 2018 May;29(5):817-826. doi: 10.1007/s13361-017-1787-8. Epub 2017 Sep 9.
In the present work, the potential of trapped ion mobility spectrometry coupled to TOF mass spectrometry (TIMS-TOF MS) for discovery and targeted monitoring of peptide biomarkers from human-in-mouse xenograft tumor tissue was evaluated. In particular, a TIMS-MS workflow was developed for the detection and quantification of peptide biomarkers using internal heavy analogs, taking advantage of the high mobility resolution (R = 150-250) prior to mass analysis. Five peptide biomarkers were separated, identified, and quantified using offline nanoESI-TIMS-CID-TOF MS; the results were in good agreement with measurements using a traditional LC-ESI-MS/MS proteomics workflow. The TIMS-TOF MS analysis permitted peptide biomarker detection based on accurate mobility, mass measurements, and high sequence coverage for concentrations in the 10-200 nM range, while simultaneously achieving discovery measurements of not initially targeted peptides as markers from the same proteins and, eventually, other proteins. Graphical Abstract ᅟ.
在本工作中,评估了离子淌度谱联用飞行时间质谱(TIMS-TOF MS)在从人源异种移植肿瘤组织中发现和靶向监测肽生物标志物方面的潜力。特别是,开发了一种 TIMS-MS 工作流程,用于使用内部重原子标记物检测和定量肽生物标志物,利用高迁移率分辨率(R = 150-250)在质量分析之前进行。使用离线纳升电喷雾 TIMS-CID-TOF MS 分离、鉴定和定量了 5 种肽生物标志物;结果与使用传统 LC-ESI-MS/MS 蛋白质组学工作流程的测量结果非常吻合。TIMS-TOF MS 分析允许基于准确的迁移率、质量测量和高序列覆盖度进行肽生物标志物检测,检测浓度范围为 10-200 nM,同时还可以作为来自相同蛋白质的标记物进行初始未靶向肽的发现测量,最终还可以进行其他蛋白质的发现测量。