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用于癌细胞系验证研究的53种多重靶向蛋白质组学检测方法的表征

Characterization of 53 Multiplexed Targeted Proteomics Assays for Verification Studies in Cancer Cell Lines.

作者信息

Sobsey Constance A, Batist Gerald, Borchers Christoph H

机构信息

Segal Cancer Proteomics Centre, Lady Davis Institute for Medical Research, Jewish General Hospital and McGill University, Montreal, Quebec H3T 1E2, Canada.

Division of Experimental Medicine, McGill University, Montreal, Quebec H3T 1E2, Canada.

出版信息

J Proteome Res. 2025 Feb 7;24(2):459-471. doi: 10.1021/acs.jproteome.4c00576. Epub 2025 Jan 13.

DOI:10.1021/acs.jproteome.4c00576
PMID:39804228
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11812018/
Abstract

The National Cancer Institute's Clinical Proteomics Tumor Analysis Consortium (CPTAC) was established to address the need for improved design, standardization, and validation of proteomics assays to enable better translation of biomarkers from the analytical lab to the clinic. Here, we applied CPTAC guidelines to characterize quantitative mass spectrometry (MS) assays in a new multiple reaction monitoring (MRM) proteomics panel. The panel of 50 proteins was developed in response to a previous study that identified a proteomic profile of altered translational control associated with response to a new cancer drug. MRM-MS assays for 53 peptides of interest were developed, optimized, and characterized on a UPLC system coupled to a triple-quadrupole mass spectrometer (QQQ-MS) using synthetic proteotypic peptides and corresponding stable-isotope labeled internal standard (SIS) peptides. Most of the assays were found to be fit-for-purpose for biomarker verification in that they precisely and reproducibly quantify the peptides at levels corresponding to the endogenous concentration in the desired cancer cell lines. Of these, 28 peptide assays represent to proteins that previously had no associated assays published in the CPTAC database. The targeted proteins in this publicly deposited validated multiplexed panel may be of use for research applications in cancer, cellular stress, neurology, cardiology, and metabolism.

摘要

美国国立癌症研究所的临床蛋白质组肿瘤分析联盟(CPTAC)的成立,是为了满足改进蛋白质组学检测的设计、标准化和验证的需求,以便更好地将生物标志物从分析实验室转化应用于临床。在此,我们应用CPTAC指南,对一个新的多反应监测(MRM)蛋白质组学检测板中的定量质谱(MS)检测进行了表征。这个包含50种蛋白质的检测板是针对之前一项研究开发的,该研究确定了一种与对一种新型癌症药物的反应相关的翻译控制改变的蛋白质组学特征。使用合成的蛋白质型肽和相应的稳定同位素标记内标(SIS)肽,在与三重四极杆质谱仪(QQQ-MS)联用的超高效液相色谱(UPLC)系统上,开发、优化并表征了针对53种目标肽的MRM-MS检测方法。发现大多数检测方法适用于生物标志物验证,因为它们能够在与所需癌细胞系内源性浓度相对应的水平上精确且可重复地定量肽。其中,28种肽检测方法所对应的蛋白质在CPTAC数据库中此前没有相关检测方法发表。这个公开存放的经过验证的多重检测板中的目标蛋白质,可能在癌症、细胞应激、神经学、心脏病学和代谢等研究应用中有用。

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Targeted and Untargeted Proteomics Approaches in Biomarker Development.靶向和非靶向蛋白质组学方法在生物标志物开发中的应用。
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