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基于增强样本多重化的靶向蛋白质组学与智能数据采集技术

Enhanced Sample Multiplexing-Based Targeted Proteomics with Intelligent Data Acquisition.

机构信息

Department of cell biology, Harvard Medical School, Boston, Massachusetts 02115, United States.

Department of biochemistry and molecular biotechnology, University of Massachusetts Chan Medical School, Worcester, Massachusetts 01605, United States.

出版信息

J Am Soc Mass Spectrom. 2024 Oct 2;35(10):2420-2428. doi: 10.1021/jasms.4c00234. Epub 2024 Sep 10.

Abstract

Targeted proteomics has been playing an increasingly important role in hypothesis-driven protein research and clinical biomarker discovery. We previously created a workflow, Tomahto, to enable real-time targeted pathway proteomics assays using two-dimensional multiplexing technology. Coupled with the TMT 11-plex reagent, hundreds of proteins of interest from up to 11 samples can be targeted and accurately quantified in a single-shot experiment with remarkable sensitivity. However, room remains to further improve the sensitivity, accuracy, and throughput, especially for targeted studies demanding a high peptide-level success rate. Here, bearing in mind the goal to improve peptide-level targeting, we introduce several new functionalities in Tomahto, featuring the integration of gas-phase fractionation using the FAIMS device, an accompanying software program (TomahtoPrimer) to customize fragmentation for each peptide target, and support for higher multiplexing capacity with the latest TMTpro reagent. We demonstrate that adding these features to the Tomahto platform significantly improves overall success rate from 89% to 98% in a single 60 min targeted assay of 290 peptides across human cell lines, while boosting quantitative accuracy via reducing TMT reporter ion interference.

摘要

靶向蛋白质组学在基于假说的蛋白质研究和临床生物标志物发现中发挥着越来越重要的作用。我们之前创建了一个工作流程,Tomahto,利用二维多重化技术实现实时靶向通路蛋白质组学检测。与 TMT 11-plex 试剂结合使用,多达 11 个样本中的数百种感兴趣的蛋白质可以在单次实验中靶向并精确定量,具有显著的灵敏度。然而,仍有空间进一步提高灵敏度、准确性和通量,特别是对于需要高肽水平成功率的靶向研究。在这里,为了提高肽水平的靶向性,我们在 Tomahto 中引入了几个新功能,包括使用 FAIMS 设备进行气相分馏、配套的软件程序(TomahtoPrimer)为每个肽靶标定制碎片化以及支持最新的 TMTpro 试剂进行更高的多重化能力。我们证明,在单个 60 分钟靶向测定中,将这些功能添加到 Tomahto 平台中,可将人类细胞系中 290 个肽的总体成功率从 89%显著提高到 98%,同时通过减少 TMT 报告离子干扰来提高定量准确性。

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