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基于质谱的生物标志物发现、验证及确认——蛋白质生物标志物检测的质量保证与控制

Mass spectrometry based biomarker discovery, verification, and validation--quality assurance and control of protein biomarker assays.

作者信息

Parker Carol E, Borchers Christoph H

机构信息

University of Victoria - Genome British Columbia Proteomics Centre, Vancouver Island Technology Park, #3101 - 4464 Markham St., Victoria, BC V8Z 7X8, Canada.

University of Victoria - Genome British Columbia Proteomics Centre, Vancouver Island Technology Park, #3101 - 4464 Markham St., Victoria, BC V8Z 7X8, Canada; Department of Biochemistry and Microbiology, University of Victoria, Petch Building Room 207, 3800 Finnerty Rd., Victoria, BC V8P 5C2, Canada.

出版信息

Mol Oncol. 2014 Jun;8(4):840-58. doi: 10.1016/j.molonc.2014.03.006. Epub 2014 Mar 20.

Abstract

In its early years, mass spectrometry (MS)-based proteomics focused on the cataloging of proteins found in different species or different tissues. By 2005, proteomics was being used for protein quantitation, typically based on "proteotypic" peptides which act as surrogates for the parent proteins. Biomarker discovery is usually done by non-targeted "shotgun" proteomics, using relative quantitation methods to determine protein expression changes that correlate with disease (output given as "up-or-down regulation" or "fold-increases"). MS-based techniques can also perform "absolute" quantitation which is required for clinical applications (output given as protein concentrations). Here we describe the differences between these methods, factors that affect the precision and accuracy of the results, and some examples of recent studies using MS-based proteomics to verify cancer-related biomarkers.

摘要

在其早期,基于质谱(MS)的蛋白质组学专注于对不同物种或不同组织中发现的蛋白质进行编目。到2005年,蛋白质组学开始用于蛋白质定量,通常基于作为母体蛋白质替代物的“蛋白型”肽。生物标志物的发现通常通过非靶向“鸟枪法”蛋白质组学进行,使用相对定量方法来确定与疾病相关的蛋白质表达变化(以“上调或下调”或“增加倍数”给出结果)。基于MS的技术还可以进行临床应用所需的“绝对”定量(以蛋白质浓度给出结果)。在这里,我们描述了这些方法之间的差异、影响结果精度和准确性的因素,以及一些使用基于MS的蛋白质组学来验证癌症相关生物标志物的近期研究实例。

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