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β-D-木糖苷介导的基底膜蛋白聚糖合成改变。

beta-D-xyloside-mediated alteration in the synthesis of basement membrane proteoglycan.

作者信息

Ledbetter S R, Hassell J R

出版信息

Arch Biochem Biophys. 1986 Apr;246(1):403-10. doi: 10.1016/0003-9861(86)90486-8.

Abstract

The effect of nitrophenyl-beta-D-xyloside (xyloside), a synthetic initiator of glycosaminoglycan synthesis, on proteoglycan and glycosaminoglycan synthesis by a basement membrane producing tumor was studied. While xyloside markedly stimulated the formation of chondroitin sulfate chains, it depressed the formation of a basement membrane heparan sulfate proteoglycan and caused only little formation of free heparan sulfate chains. However, when the synthesis of the core protein of the proteoglycan was inhibited by cycloheximide, heparan sulfate chains were produced by xyloside treatment. These heparan sulfate chains had a sulfate content higher than that of heparan sulfate found on the proteoglycan. The data indicate that xyloside can substitute for the heparan sulfate initiation site on the core protein of the proteoglycan and that this initiation is enhanced in the absence of core protein. This suggests that under normal conditions the formation of heparan sulfate chains may be tightly linked to the production of the core protein.

摘要

研究了糖胺聚糖合成的合成引发剂硝基苯基-β-D-木糖苷(木糖苷)对产生基底膜的肿瘤中蛋白聚糖和糖胺聚糖合成的影响。虽然木糖苷显著刺激了硫酸软骨素链的形成,但它抑制了基底膜硫酸乙酰肝素蛋白聚糖的形成,并且仅导致少量游离硫酸乙酰肝素链的形成。然而,当用环己酰亚胺抑制蛋白聚糖核心蛋白的合成时,木糖苷处理可产生硫酸乙酰肝素链。这些硫酸乙酰肝素链的硫酸盐含量高于蛋白聚糖上发现的硫酸乙酰肝素。数据表明,木糖苷可以替代蛋白聚糖核心蛋白上的硫酸乙酰肝素起始位点,并且在没有核心蛋白的情况下这种起始作用会增强。这表明在正常条件下,硫酸乙酰肝素链的形成可能与核心蛋白的产生紧密相关。

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