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本文引用的文献

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Liquid chromatography high-resolution TOF analysis: investigation of MSE for broad-spectrum drug screening.液相色谱高分辨飞行时间分析:用于广谱药物筛选的 MSE 研究。
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Glycoproteomic analysis of prostate cancer tissues by SWATH mass spectrometry discovers N-acylethanolamine acid amidase and protein tyrosine kinase 7 as signatures for tumor aggressiveness.通过SWATH质谱法对前列腺癌组织进行糖蛋白质组学分析发现,N-酰基乙醇胺酸酰胺酶和蛋白酪氨酸激酶7是肿瘤侵袭性的标志物。
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Demonstrating the feasibility of large-scale development of standardized assays to quantify human proteins.展示大规模开发标准化检测方法以定量测定人体蛋白质的可行性。
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Plasma Proteome Database as a resource for proteomics research: 2014 update.血浆蛋白质组数据库作为蛋白质组学研究的资源:2014 年更新。
Nucleic Acids Res. 2014 Jan;42(Database issue):D959-65. doi: 10.1093/nar/gkt1251. Epub 2013 Dec 3.
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A highly sensitive targeted mass spectrometric assay for quantification of AGR2 protein in human urine and serum.一种用于定量检测人尿液和血清中AGR2蛋白的高灵敏度靶向质谱分析法。
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Identification of a seven glycopeptide signature for malignant pleural mesothelioma in human serum by selected reaction monitoring.通过选择反应监测鉴定人血清中恶性胸膜间皮瘤的七个糖肽标志物。
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Technical considerations for large-scale parallel reaction monitoring analysis.大规模平行反应监测分析的技术考量
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Selected reaction monitoring mass spectrometry: a methodology overview.选择反应监测质谱法:方法概述。
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Solid phase extraction of N-linked glycopeptides using hydrazide tip.使用酰肼基探针进行 N-连接糖肽的固相萃取。
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Statistical design for biospecimen cohort size in proteomics-based biomarker discovery and verification studies.基于蛋白质组学的生物标志物发现和验证研究中生物样本队列大小的统计设计。
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靶向蛋白质组学:发现与验证之间的桥梁。

Targeted proteomics: a bridge between discovery and validation.

作者信息

Harlan Robert, Zhang Hui

机构信息

Department of Pathology, Johns Hopkins University, Baltimore, MD 21231, USA.

出版信息

Expert Rev Proteomics. 2014 Dec;11(6):657-61. doi: 10.1586/14789450.2014.976558. Epub 2014 Oct 28.

DOI:10.1586/14789450.2014.976558
PMID:25348939
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4490831/
Abstract

New technologies in mass spectrometry are beginning to mature and show unique advantages for the identification and quantitation of proteins. In recent years, one of the significant goals of clinical proteomics has been to identify biomarkers that can be used for clinical diagnosis. As technology has progressed, the list of potential biomarkers has grown. However, the verification and validation of these potential biomarkers is increasingly challenging and require high-throughput quantitative assays, targeting specific candidates. Targeted proteomics bridges the gap between biomarker discovery and the development of clinically applicable biomarker assays.

摘要

质谱新技术正开始走向成熟,并在蛋白质鉴定和定量方面展现出独特优势。近年来,临床蛋白质组学的一个重要目标是识别可用于临床诊断的生物标志物。随着技术的进步,潜在生物标志物的清单不断增加。然而,对这些潜在生物标志物的验证和确认越来越具有挑战性,需要针对特定候选物的高通量定量分析。靶向蛋白质组学填补了生物标志物发现与临床适用生物标志物检测方法开发之间的空白。