Effect of Phosphorylation on the Collision Cross Sections of Peptide Ions in Ion Mobility Spectrometry

Q3 Physics and Astronomy
Kosuke Ogata, Chih-Hsiang Chang, Y. Ishihama
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引用次数: 8

Abstract

The insertion of ion mobility spectrometry (IMS) between LC and MS can improve peptide identification in both proteomics and phosphoproteomics by providing structural information that is complementary to LC and MS, because IMS separates ions on the basis of differences in their shapes and charge states. However, it is necessary to know how phosphate groups affect the peptide collision cross sections (CCS) in order to accurately predict phosphopeptide CCS values and to maximize the usefulness of IMS. In this work, we systematically characterized the CCS values of 4,433 pairs of mono-phosphopeptide and corresponding unphosphorylated peptide ions using trapped ion mobility spectrometry (TIMS). Nearly one-third of the mono-phosphopeptide ions evaluated here showed smaller CCS values than their unphosphorylated counterparts, even though phosphorylation results in a mass increase of 80 Da. Significant changes of CCS upon phosphorylation occurred mainly in structurally extended peptides with large numbers of basic groups, possibly reflecting intramolecular interactions between phosphate and basic groups.
离子迁移谱法中磷酸化对肽离子碰撞截面的影响
离子迁移率谱法(IMS)在LC和MS之间的插入,通过提供与LC和MS互补的结构信息,可以提高蛋白质组学和磷蛋白质组学中的肽鉴定,因为IMS是根据离子的形状和电荷状态的差异来分离离子的。然而,为了准确预测肽碰撞截面(CCS)值,最大限度地发挥IMS的作用,有必要了解磷酸基对肽碰撞截面(CCS)的影响。在这项工作中,我们系统地表征了4,433对单肽和相应的未磷酸化肽离子的CCS值,使用捕获离子迁移谱法(TIMS)。这里评估的近三分之一的单磷酸肽离子比未磷酸化的离子显示出更小的CCS值,即使磷酸化导致质量增加80 Da。磷酸化后CCS的显著变化主要发生在具有大量碱性基团的结构延伸肽中,这可能反映了磷酸盐与碱性基团之间的分子内相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mass spectrometry
Mass spectrometry Physics and Astronomy-Instrumentation
CiteScore
1.90
自引率
0.00%
发文量
3
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