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Deuterium Isobaric Amine-Reactive Tags for Quantitative Proteomics

机译:氘等压胺反应标签用于定量蛋白质组学

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This paper demonstrates the applications of a novel isobaric reagent, named deuterium (~(2)H) isobaric amine-reactive tag (DiART), for quantitative proteomics. Peptides labeled with DiART were analyzed using an electrospray ionization (ESI)-based LTQ-Orbitrap mass spectrometer. Our data showed that ~(2)H-associated isotope effects, such as partial loss of ~(2)H labels during tandem mass spectrometry (MS/MS) and ~(2)H-related chromatographic shift, were either not observed or negligible. With the use of a hybrid collision-induced dissociation (CID)-higher energy C-trap dissociation (HCD) acquisition method, we were able to identify DiART-labeled peptides with high confidence and quantify them with high accuracy. Furthermore, we adopted a hybrid electron-transfer dissociation (ETD)-HCD acquisition protocol and developed a novel data analysis approach to measure phosphorylation of peptides. Our results showed DiART had excellent performance on LTQ-Orbitrap instruments and provided a cost-effective technique for large-scale quantitative proteomics measurements.
机译:本文演示了一种新型的等压试剂,称为氘(〜(2)H)等压胺反应标签(DiART),用于定量蛋白质组学。使用基于电喷雾电离(ESI)的LTQ-Orbitrap质谱仪分析被DiART标记的肽。我们的数据表明,未观察到或未观察到〜(2)H相关的同位素效应,例如在串联质谱(MS / MS)中〜(2)H标签的部分丢失和〜(2)H相关的色谱位移。微不足道。通过使用混合碰撞诱导解离(CID)-高能C阱解离(HCD)采集方法,我们能够以高可信度鉴定DiART标记的肽并进行高精度定量。此外,我们采用了混合电子转移解离(ETD)-HCD采集协议,并开发了一种新颖的数据分析方法来测量肽的磷酸化。我们的结果表明DiART在LTQ-Orbitrap仪器上具有出色的性能,并为大规模定量蛋白质组学测量提供了一种经济高效的技术。

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