van Pelt J, Kamerling J P, Vliegenthart J F, Hoogeveen A T, Galjaard H
Department of Bio-Organic Chemistry, Utrecht University, The Netherlands.
Clin Chim Acta. 1988 Jun 15;174(3):325-35. doi: 10.1016/0009-8981(88)90059-9.
Sialic acid-containing storage material was isolated from cultured human galactosialidosis fibroblasts, by a combination of gel filtration and anion-exchange chromatography on Mono Q. The obtained sialyloligosaccharides were analyzed by 500-MHz 1H-NMR spectroscopy in combination with sugar analysis and analytical HPLC. The storage material consisted of a series of completely sialylated N-acetyl-lactosamine type of structures having Man beta 1-4GlcNAc at the reducing terminus in common, similar to those recently reported for human sialidosis fibroblasts. Comparison of the storage material from both sources revealed only differences in their relative amounts. In control fibroblasts these compounds could not be detected. The nature of the accumulated compounds is in accordance with the alpha-neuraminidase deficiency in both genetic diseases. The additional deficiency of beta-galactosidase in case of galactosialidosis is not reflected in the storage material.
通过在Mono Q上进行凝胶过滤和阴离子交换色谱相结合的方法,从培养的人类半乳糖唾液酸贮积症成纤维细胞中分离出含唾液酸的贮存物质。对获得的唾液酸寡糖进行了500兆赫的1H-NMR光谱分析,并结合糖分析和分析型高效液相色谱法。贮存物质由一系列完全唾液酸化的N-乙酰乳糖胺型结构组成,其还原端均有Manβ1-4GlcNAc,这与最近报道的人类唾液酸贮积症成纤维细胞的结构相似。对两种来源的贮存物质进行比较,发现仅相对含量存在差异。在对照成纤维细胞中未检测到这些化合物。所积累化合物的性质与这两种遗传性疾病中的α-神经氨酸酶缺乏症相符。在半乳糖唾液酸贮积症中β-半乳糖苷酶的额外缺乏在贮存物质中未体现出来。