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从头糖链测序的电子激发解离和固定电荷衍生化。

De Novo Glycan Sequencing by Electronic Excitation Dissociation and Fixed-Charge Derivatization.

机构信息

Center for Biomedical Mass Spectrometry , Boston University School of Medicine , Boston , Massachusetts 02118 , United States.

Department of Chemistry , Boston University , Boston , Massachusetts 02215 , United States.

出版信息

Anal Chem. 2018 Mar 20;90(6):3793-3801. doi: 10.1021/acs.analchem.7b04077. Epub 2018 Feb 27.

Abstract

Detailed glycan structural characterization is frequently achieved by collisionally activated dissociation (CAD) based sequential tandem mass spectrometry (MS ) analysis of permethylated glycans. However, it is challenging to implement MS ( n > 2) during online glycan separation, and this has limited its application to analysis of complex glycan mixtures from biological samples. Further, permethylation can reduce liquid chromatographic (LC) resolution of isomeric glycans. Here, we studied the electronic excitation dissociation (EED) fragmentation behavior of native glycans with a reducing-end fixed charge tag and identified key spectral features that are useful for topology and linkage determination. We also developed a de novo glycan sequencing software that showed remarkable accuracy in glycan topology elucidation based on the EED spectra of fixed charge-derivatized glycans. The ability to obtain glycan structural details at the MS level, without permethylation, via a combination of fixed charge derivatization, EED, and de novo spectral interpretation, makes the present approach a promising tool for comprehensive and rapid characterization of glycan mixtures.

摘要

详细的糖链结构特征通常通过对全甲基化糖进行基于碰撞激活解离(CAD)的顺序串联质谱(MS)分析来实现。然而,在在线糖分离过程中实施 MS(n>2)具有挑战性,这限制了其在分析生物样品中复杂糖混合物的应用。此外,全甲基化会降低异构糖的液相色谱(LC)分辨率。在这里,我们研究了带有还原端固定电荷标记的天然糖的电子激发解离(EED)碎裂行为,并确定了用于拓扑和键合确定的关键光谱特征。我们还开发了一种从头开始的聚糖测序软件,该软件基于固定电荷衍生化聚糖的 EED 光谱,在聚糖拓扑结构阐明方面表现出了显著的准确性。通过固定电荷衍生化、EED 和从头开始的光谱解释相结合,无需全甲基化即可在 MS 水平上获得聚糖结构细节的能力,使得该方法成为全面快速表征聚糖混合物的有前途的工具。

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