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Peptide Quantification Using 8-Plex Isobaric Tags and Electron Transfer Dissociation Tandem Mass Spectrometry

机译:使用8重等压标记和电子转移解离串联质谱进行肽定量

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摘要

Isobaric tags for absolute and relative quantitation (iTRAQ) allow for simultaneous relative quantification of peptides from up to eight different samples. Typically peptides labeled with 8-plex iTRAQ tags are pooled and fragmented using beam-type collision activated dissociation (CAD) which, in addition to cleaving the peptide backbone bonds, cleaves the tag to produce reporter ions. The relative intensities of the reporters are directly proportional to the relative abundances of each peptide in the solution phase. Recently, studies using the 4-plex iTRAQ tagging reagent demonstrated that electron transfer dissociation (ETD) of 4-plex iTRAQ labeled peptides cleaves at the N-C(alpha) bond in the tag and allows for up to three channels of quantification. In this paper we investigate the ETD fragmentation patterns of peptides labeled with 8-plex iTRAQ tags. We demonstrate that upon ETD, peptides labeled with 8-plex iTRAQ tags fragment to produce unique reporter ions that allow for five channels of quantification. ETD-MS/MS of these labeled peptides also produces a peak at 322 m/z which, upon resonant excitation (CAD), gives rise to all eight iTRAQ reporter ions and allows for eight channels of quantification. Comparison of this method to beam-type CAD quantification shows a good correlation (y velence 0.91x + 0.01, R~(2) velence 0.9383).
机译:绝对和相对定量(iTRAQ)的等压标签可同时对多达8个不同样品中的肽进行相对定量。通常,使用束线型碰撞激活解离(CAD)合并并标记有8重iTRAQ标签的肽片段,该片段除切割肽主链键外,还切割标签以产生报告离子。报告分子的相对强度与溶液相中每种肽的相对丰度成正比。最近,使用4-plex iTRAQ标记试剂的研究表明4-plex iTRAQ标记的肽的电子转移解离(ETD)在标签的N-Cα键处裂解,并允许多达三个定量通道。在本文中,我们研究了用8重iTRAQ标签标记的肽的ETD片段化模式。我们证明,在ETD上,用8重iTRAQ标签标记的肽片段会产生独特的报告离子,从而允许五个定量通道。这些标记肽的ETD-MS / MS也会在322 m / z处产生一个峰,该峰在共振激发(CAD)时会产生所有八个iTRAQ报告离子,并允许八个定量通道。将该方法与光束型CAD量化进行比较显示出良好的相关性(y velence 0.91x + 0.01,R〜(2)velence 0.9383)。

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