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首页> 外文期刊>Neurochemical Research >Structural Characterization of Monosialo-, Disialo- and Trisialo-gangliosides by Negative Ion AP-MALDI-QIT-TOF Mass Spectrometry with MSn Switching
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Structural Characterization of Monosialo-, Disialo- and Trisialo-gangliosides by Negative Ion AP-MALDI-QIT-TOF Mass Spectrometry with MSn Switching

机译:MSn 切换负离子AP-MALDI-QIT-TOF质谱分析单唾液酸,二唾液酸和三唾液酸神经节苷脂的结构特征

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摘要

The atmospheric pressure matrix-assisted laser desorption/ionization (AP-MALDI) is a quite convenient soft ionization for biomolecules, keeping analytes atmospheric conditions instead of high vacuum conditions. In this study, an AP-MALDI ion source has been coupled to a quadrupole ion trap time-of-flight (QIT-TOF) mass spectrometer, which is able to perform MSn analysis. We applied this system to the structural characterization of monosialogangliosides, GM1 (NeuAc) and GM2 (NeuAc), disialogangliosides, GD2 (NeuAc, NeuAc), GD1a (NeuAc, NeuAc) and GD1b (NeuAc, NeuAc) and trisialoganglioside GT1a (NeuAc, NeuAc, NeuAc). In this system, the negative ion mass spectra of MS, MS2 and MS3, a set of three mass spectra, were able to measure within 2 s per cycle. Thus, obtained results demonstrate that the negative ion mode MS, MS2 and MS3 spectra provided sufficient information for the determination of molecular weights, oligosaccharide sequences and ceramide structures, and indicate that the AP-MALDI-QIT-TOF mass spectrometry keeping analytes atmospheric conditions with MSn switching is quite useful and convenient for structural analyses of various types of sialic acid-containing GSLs, gangliosides.
机译:大气压基质辅助激光解吸/电离(AP-MALDI)是一种非常方便的生物分子软电离,可保持分析物处于大气条件而不是高真空条件。在这项研究中,将AP-MALDI离子源与四极杆离子阱飞行时间(QIT-TOF)质谱仪耦合,该质谱仪能够执行MSn 分析。我们将此系统应用于单唾液酸神经节苷脂,GM1(NeuAc)和GM2(NeuAc),二唾液酸神经节苷脂,GD2(NeuAc,NeuAc),GD1a(NeuAc,NeuAc)和GD1b(NeuAc,NeuAc)和三唾液酸神经节苷脂GT1a(NeuAc, ,NeuAc)。在该系统中,MS,MS2 和MS3 (一组三个质谱图)的负离子质谱图能够在每个循环2 s内进行测量。因此,获得的结果表明,负离子模式MS,MS2 和MS3 谱图为测定分子量,寡糖序列和神经酰胺结构提供了足够的信息,并表明AP-MALDI-QIT- TOF质谱通过MSn 切换保持分析物处于大气状态,对于各种类型的含唾液酸的GSL,神经节苷脂的结构分析非常有用且方便。

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  • 来源
    《Neurochemical Research 》 |2012年第6期| p.1315-1324| 共10页
  • 作者单位

    Disease Glycomics Team, Systems Glycobiology Research Group, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan;

    Shimadzu Corporation, 1 Nishinokyo-Kuwabaracho, Nakagyo-ku, Kyoto, 604-8511, Japan;

    Shimadzu Corporation, 1 Nishinokyo-Kuwabaracho, Nakagyo-ku, Kyoto, 604-8511, Japan;

    Shimadzu Corporation, 1 Nishinokyo-Kuwabaracho, Nakagyo-ku, Kyoto, 604-8511, Japan;

    Glycan Recognition Team, Systems Glycobiology Research Group, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan;

    School of Pharmacy, Kinki University, 3-4-1 Kowakae, Higashi-Osaka, 577-8502, Japan;

    Shimadzu Corporation, 1 Nishinokyo-Kuwabaracho, Nakagyo-ku, Kyoto, 604-8511, Japan;

    Disease Glycomics Team, Systems Glycobiology Research Group, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan;

    Institute of Glycoscience, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa, 259-1292, Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    AP-MALDI; Negative ion; Mass spectrometry; Gangliosides; MSn switching;

    机译:AP-MALDI;负离子;质谱;神经节苷脂;MSn转换;

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