[人类n -糖蛋白聚糖结构的预测]。

G Strecker, J Montreuil
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引用次数: 0

摘要

通过将β -(1导致4)- glcnac - β -(1导致)- asn或α Fuc-(1导致6或3)- β -(1导致4)- glcnac - β -(1导致)- asn序列添加到从甘露甘露病、聚焦病和唾液病的人尿液中分离的低聚糖中,我们能够重建许多天冬酰胺聚糖的结构。我们假设i)这些尚未被表征的结构预先存在于人类糖蛋白的聚糖中,可能存在于细胞质或/和细胞膜中;ii)它们是内切- n -乙酰氨基葡萄糖苷酶作用的产物,由于缺乏外糖苷酶而受到保护,并在细胞中积累,然后在尿液中积累。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prediction of glycan structures of human N-glycoproteins].

By adding the sequence beta-(1 leads to 4)-GlcNAc-beta-(1 leads to)-Asn or alpha Fuc-(1 leads to 6 or 3)-beta-(1 leads to 4)-GlcNAc-beta-(1 leads to)-Asn to the oligosaccharides isolated from human urines of mannosidosis, fucosidosis and sialidosis, we are able to reconstitute numerous structures of asparaginyl-glycans. We postulate i) that these structures which have not yet been characterized pre-exist in glycans of human glycoproteins, probably in the cytoplasm or/and the cell membrane; ii) that they are products of the action of endo-beta-N-acetyl-glucosaminidases which are protected because of the lack of exoglycosidases and accumulate in the cells, and then in the urine.

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