Hanisch F G, Chai W, Rosankiewicz J R, Lawson A M, Stoll M S, Feizi T
Institute of Immunobiology, University Clinic of Cologne, Germany.
Eur J Biochem. 1993 Oct 15;217(2):645-55. doi: 10.1111/j.1432-1033.1993.tb18288.x.
Mucins from the pooled gastric juice of Lewis-positive secretors were investigated to establish their glycosylation patterns with particular reference to the type and abundance of the glycan-core structures. Following reductive beta-elimination, the neutral glycan alditols from these mucins were fractionated by ion exchange and size-exclusion chromatographies and subjected to structural analyses. It was possible to gain insights into the core sequences of the neutral O-linked glycan alditols by matching (a) composition data from liquid secondary-ion mass spectrometry of the native alditol fractions, (b) specific structural information on the core sequences by thin-layer-chromatography mass spectrometry of alditol-derived neoglycolipids and (c) data from electron-impact mass spectrometry of permethylated glycan alditols or their partially methylated alditol acetates. The predominant core structures detected among the neutral glycans representing about 77% (by mass) of the total carbohydrates released from gastric mucins were core 1, Gal beta 1-3GalNAc (Ac, acetyl) and core 2, Gal beta 1-3(GlcNAc beta 1-6)GalNAc in the approximate ratio 1:2. Core 3, GlcNAc beta 1-3GalNAc, and core 4, GlcNAc beta 1-3(GlcNAc beta 1-6)GalNAc, were much less abundant (< 10%), while core 5, GalNAc alpha 1-3GalNAc, core 6, GlcNAc beta 1-6GalNAc, and a recently described sequence GalNAc alpha 1-6GalNAc (core 7) were not detected. This investigation also addressed the question of the presence of the sequence Gal beta 1-6GalNAc which has been reported previously to occur as a core-structure element in gastric mucins. This was greatly assisted by the availability of the authentic chemically synthetized disaccharide alditol which, when converted into a neoglycolipid after mild periodate oxidation, gives diagnostic ions in mass spectrometry and can be detected with high sensitivity. No evidence was found for the presence of this unusual sequence among the oligosaccharides in gastric mucins.
对来自Lewis阳性分泌者的混合胃液中的粘蛋白进行了研究,以确定其糖基化模式,特别关注聚糖核心结构的类型和丰度。经过还原β-消除后,通过离子交换和尺寸排阻色谱法对这些粘蛋白中的中性聚糖糖醇进行分离,并进行结构分析。通过匹配以下内容,可以深入了解中性O-连接聚糖糖醇的核心序列:(a) 天然糖醇馏分的液体二次离子质谱的组成数据;(b) 糖醇衍生的新糖脂的薄层色谱质谱提供的关于核心序列的特定结构信息;(c) 全甲基化聚糖糖醇或其部分甲基化糖醇乙酸酯的电子轰击质谱数据。在占胃粘蛋白释放的总碳水化合物约77%(按质量计)的中性聚糖中检测到的主要核心结构是核心1,Galβ1-3GalNAc(Ac,乙酰基)和核心2,Galβ1-3(GlcNAcβ1-6)GalNAc,比例约为1:2。核心3,GlcNAcβ1-3GalNAc和核心4,GlcNAcβ1-3(GlcNAcβ1-6)GalNAc的丰度要低得多(<10%),而核心5,GalNAcα1-3GalNAc,核心6,GlcNAcβ1-6GalNAc,以及最近描述的序列GalNAcα1-6GalNAc(核心7)未被检测到。这项研究还探讨了Galβ1-6GalNAc序列的存在问题,该序列先前曾被报道为胃粘蛋白中的核心结构元件。 authentic化学合成二糖糖醇的可用性极大地帮助了这一研究,该二糖糖醇在温和的高碘酸盐氧化后转化为新糖脂时,在质谱中给出诊断离子,并且可以高灵敏度检测到。在胃粘蛋白的寡糖中没有发现这种不寻常序列存在的证据。