腹足动物的中性n -聚糖。

Martin Gutternigg, Karin Ahrer, Heidi Grabher-Meier, Sabine Bürgmayr, Erika Staudacher
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引用次数: 39

摘要

通过蛋白水解消化、肽释放、2-氨基吡啶荧光标记、电荷、大小、疏水性等分离得到纯糖结构,对腹足动物(Arion lusitanicus,腹足动物)皮肤、内脏和蛋糖蛋白的中性n -聚糖结构进行检测。采用二维高效液相色谱法(大小和疏水性)和MALDI-TOF质谱法分析了多糖在特定外糖苷酶消化前后的位置和键合。成体组织中最显著的特征是含有大量的寡甘露糖甙和以3- o甲基化甘露糖末端的小的少甘露糖甙聚糖。截断的结构通常包含由β 1,2连接木糖对-甘露糖残基和/或最内层GlcNAc残基的α -聚焦化(主要是α 1,6-)对内核的修饰。皮肤和内脏主要显示相同的聚糖,但不同的量。还检测到携带3- o甲基化半乳糖的大型结构的痕迹。鸡蛋聚糖主要含有(约75%)寡糖结构和一些被木糖或α 1,6-修饰的少糖糖结构,但在这种情况下没有检测到任何单糖的甲基化。因此,腹足类动物似乎能够产生多种类型的结构,从典型的人类结构到类似于线虫的结构,因此将成为理解糖基化调控的有价值的模型。此外,这为利用这种生物作为宿主生产重组蛋白开辟了道路。糖基化的详细知识也有助于确定害虫防治的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neutral N-glycans of the gastropod Arion lusitanicus.

The neutral N-glycan structures of Arion lusitanicus (gastropod) skin, viscera and egg glycoproteins were examined after proteolytic digestion, release of the glycans from the peptides, fluorescent labelling with 2-aminopyridine and fractionation by charge, size and hydrophobicity to obtain pure glycan structures. The positions and linkages of the sugars in the glycan were analysed by two dimensional HPLC (size and hydrophobicity) and MALDI-TOF mass spectrometry before and after digestion with specific exoglycosidases. The most striking feature in the adult tissues was the high amount of oligomannosidic and small paucimannosidic glycans terminated with 3-O-methylated mannoses. The truncated structures often contained modifications of the inner core by beta1,2-linked xylose to the beta-mannose residue and/or an alpha-fucosylation (mainly alpha1,6-) of the innermost GlcNAc residue. Skin and viscera showed predominantly the same glycans, however, in different amounts. Traces of large structures carrying 3-O-methylated galactoses were also detected. The egg glycans contained mainly (approximately 75%) oligomannosidic structures and some paucimannosidic structures modified by xylose or alpha1,6-fucose, but in this case no methylation of any monosaccharide was detected. Thus, gastropods seem to be capable of producing many types of structures ranging from those typical in human to structures similar to those found in nematodes, and therefore will be a valuable model to understand the regulation of glycosylation. Furthermore, this opens the way for using this organism as a host for the production of recombinant proteins. The detailed knowledge on glycosylation also may help to identify targets for pest control.

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