Banazadeh Alireza, Nieman Reed, Goli Mona, Peng Wenjing, Hussein Ahmed, Bursal Ercan, Lischka Hans, Mechref Yehia
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061, USA. Email:
Department of Biotechnology, Institute of Graduate Studies and Research, University of Alexandria, Alexandria, 21526, Egypt.
RSC Adv. 2019 Jul 1;9(35):20137-20148. doi: 10.1039/c9ra02337b. Epub 2019 Jun 27.
Matrix-assisted laser desorption ionization-in source decay (MALDI-ISD) analysis is a useful technique in the structural analysis of glycans. Our recent publication demonstrated that magnetic carbon nanoparticles (MCNPs), used as a MALDI co-matrix, significantly enhanced ISD efficiency for glycomic analysis by MALDI-TOF. In this study, MCNPs were used for the structural study of isomeric glycans. Results from the standard glycans confirmed easy distinction of positional and linkage isomers without the need for further derivatization of glycan molecules. Extensive glycosidic and cross-ring fragmented ions provided different fragment patterns for various glycan isomers. Core- and branch-fucosylated isomers were distinguished by several unique ions, and pseudo-MS data were used to recognize the fucosylated branch. Although no diagnostic fragment ion was observed for 2,3- and 2,6-linked sialic acid isomers, their MALDI-ISD patterns were found to be significantly different ( < 0.05). Furthermore, the method introduced in this study could not only be used for the identification of glycan isomers but has also proved effective for the isomeric structural confirmation of gangliosides. GD1a and GD1b gangliosides were easily distinguished by the diagnostic ion originated from GD1a, produced by ZZ cleavages. Moreover, liquid chromatography coupled with MALDI-TOF was applied to analyze -glycan isomers derived from a pooled human blood serum sample, providing an alternative method of isomeric glycomic analysis of biological specimens.
基质辅助激光解吸电离源内衰变(MALDI-ISD)分析是聚糖结构分析中的一种有用技术。我们最近的出版物表明,用作MALDI共基质的磁性碳纳米颗粒(MCNPs)显著提高了通过MALDI-TOF进行糖组学分析的ISD效率。在本研究中,MCNPs用于异构聚糖的结构研究。标准聚糖的结果证实,无需对聚糖分子进行进一步衍生化,即可轻松区分位置异构体和连接异构体。广泛的糖苷键和跨环碎裂离子为各种聚糖异构体提供了不同的碎片模式。核心岩藻糖基化异构体和分支岩藻糖基化异构体通过几个独特的离子得以区分,并且利用伪质谱数据识别岩藻糖基化分支。尽管未观察到2,3-和2,6-连接的唾液酸异构体的诊断性碎片离子,但发现它们的MALDI-ISD模式存在显著差异(<0.05)。此外,本研究中引入的方法不仅可用于聚糖异构体的鉴定,而且已证明对神经节苷脂的异构体结构确证有效。GD1a和GD1b神经节苷脂可通过源自GD1a的诊断离子(由ZZ裂解产生)轻松区分。此外,液相色谱与MALDI-TOF联用用于分析来自混合人血清样本的聚糖异构体,为生物标本的异构体糖组学分析提供了一种替代方法。