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使用MSn光谱匹配对异构2-氨基吡啶衍生化寡糖进行结构归属

Structural assignment of isomeric 2-aminopyridine-derivatized oligosaccharides using MSn spectral matching.

作者信息

Takegawa Yasuhiro, Ito Shinya, Yoshioka Shinji, Deguchi Kisaburo, Nakagawa Hiroaki, Monde Kenji, Nishimura Shin-Ichiro

机构信息

Division of Biological Sciences, Graduate School of Science, Hokkaido University, Sapporo 001-0021, Japan.

出版信息

Rapid Commun Mass Spectrom. 2004;18(4):385-91. doi: 10.1002/rcm.1341.

Abstract

Two isomeric pairs of 2-aminopyridine (PA)-derivatized fucosylated and non-fucosylated oligosaccharides (complex-type N-glycans of IgG) were analyzed using liquid chromatography/ion trap mass spectrometry (LC/ITMS) with a sonic spray ionization source and by varying the collision-induced dissociation voltage. Reproducibility of MS(n) (n = 2) spectra obtained by LC/ITMS was tested considering both fragment ions (m/z) and intensities. A comparison of their MS(n) spectra and evaluation of similarities (or matching), based on correlation coefficients between MS(n) spectra, was investigated as a possibility for structural assignment of the isomers. It is shown that such MS(n) spectral matching is useful and applicable to the structural assignment of relatively large fucosylated and sialylated PA-oligosaccharides released from IgG based on Bn- and Yn-type fragmentations of the corresponding M+H+Na ions.

摘要

使用配备超声喷雾电离源的液相色谱/离子阱质谱(LC/ITMS)并通过改变碰撞诱导解离电压,分析了两对2-氨基吡啶(PA)衍生的岩藻糖基化和非岩藻糖基化寡糖(IgG的复合型N-聚糖)的异构体。考虑到碎片离子(m/z)和强度,测试了通过LC/ITMS获得的MS(n)(n = 2)光谱的重现性。基于MS(n)光谱之间的相关系数,研究了它们的MS(n)光谱比较和相似性(或匹配)评估,以此作为异构体结构归属的一种可能性。结果表明,这种MS(n)光谱匹配是有用的,并且适用于基于相应M+H+Na离子的Bn型和Yn型裂解从IgG释放的相对较大的岩藻糖基化和唾液酸化PA-寡糖的结构归属。

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