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Index-ion Triggered MS2 Ion Quantification: A Novel Proteomics Approach for Reproducible Detection and Quantification of Targeted Proteins in Complex Mixtures*

机译:索引离子触发的MS2离子定量:复杂混合物中目标蛋白的可重现检测和定量的新型蛋白质组学方法*

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摘要

Biomedical research requires protein detection technology that is not only sensitive and quantitative, but that can reproducibly measure any set of proteins in a biological system in a high throughput manner. Here we report the development and application of a targeted proteomics platform termed index-ion triggered MS2 ion quantification (iMSTIQ) that allows reproducible and accurate peptide quantification in complex mixtures. The key feature of iMSTIQ is an approach called index-ion triggered analysis (ITA) that permits the reproducible acquisition of full MS2 spectra of targeted peptides independent of their ion intensities. Accurate quantification is achieved by comparing the relative intensities of multiple pairs of fragment ions derived from isobaric targeted peptides during MS2 analysis. Importantly, the method takes advantage of the favorable performance characteristics of the LTQ-Orbitrap, which include high mass accuracy, resolution, and throughput. As such it provides an attractive targeted proteomics tool to meet the demands of systems biology research and biomarker studies.
机译:生物医学研究需要蛋白质检测技术,该技术不仅要灵敏且定量,而且要能够以高通量方式可重复地测量生物系统中的任何蛋白质组。在这里,我们报告称为靶向离子触发的MS2离子定量(iMSTIQ)的靶向蛋白质组学平台的开发和应用,该平台允许在复杂混合物中进行可重复且准确的肽定量。 iMSTIQ的关键特征是一种称为索引离子触发分析(ITA)的方法,该方法可独立于离子强度而重现捕获目标肽的完整MS2光谱。通过在MS2分析过程中比较来自等压目标肽的多对片段离子的相对强度,可以实现准确的定量。重要的是,该方法利用了LTQ-Orbitrap的良好性能特征,其中包括高质量精度,分辨率和通量。因此,它提供了一种有吸引力的靶向蛋白质组学工具,可以满足系统生物学研究和生物标记研究的需求。

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