Suppr超能文献

铁皮石斛多糖抑制人晶状体上皮细胞凋亡的核心结构。

The core structure of a Dendrobium huoshanense polysaccharide required for the inhibition of human lens epithelial cell apoptosis.

机构信息

School of Biological and Medical Engineering, Hefei University of Technology, No 193 Tunxi Road, Hefei 230009, People's Republic of China; School of Biotechnology and Food Engineering, Hefei University of Technology, People's Republic of China.

Sericultural & Agri-Food Research Institute, Guangdong Academy of Agricultural Science, Key Laboratory of Functional Foods, Ministry of Agriculture, Guangdong Key Laboratory of Agricultural Products Processing, Guangzhou 510610, People's Republic of China.

出版信息

Carbohydr Polym. 2017 Jan 2;155:252-260. doi: 10.1016/j.carbpol.2016.08.087. Epub 2016 Aug 28.

Abstract

The aim of this work was to investigate the core structure of a Dendrobium huoshanense polysaccharide DHPD1 required for the inhibition of lens epithelial cell apoptosis. In order to obtain the fragments containing the core domain, pectinase was employed to hydrolyze DHPD1. After 24h reaction, it is interesting that the hydrolyzation seemed to be stopped, leading to a final enzymatic fragment DHPD1-24 with molecular weight about 1552Da. Compared to DHPD1, although the bioactivity is decreased, DHPD1-24 remained the ability to inhibit the HO-induced apoptosis of human lens epithelial (HLE) cells via suppressing the MAPK signaling pathways. These results suggested that DHPD1-24 might be the core domain required for DHPD1 to inhibit HLE cell apoptosis. Methylation analysis showed DHPD1-24 was composed of (1→5)-linked-Araf, (1→3,6)-linked-Manp, 1-linked-Glcp, (1→4)-linked-Glcp, (1→6)-linked-Glcp, (1→4,6)-linked-Glcp, (1→6)-linked-Galp and 1-linked-Xylp in a molar ratio of 1.06:1.53:2.11:2.04:0.93:0.91:0.36:1.01. Moreover, the primary structural features of DHPD1-24 were characterized by NMR spectrum.

摘要

本工作旨在研究铁皮石斛多糖 DHPD1 抑制晶状体上皮细胞凋亡所需的核心结构。为了获得含有核心结构域的片段,使用果胶酶水解 DHPD1。经过 24 小时反应,有趣的是,水解似乎停止了,最终得到分子量约为 1552Da 的酶解片段 DHPD1-24。与 DHPD1 相比,尽管生物活性降低,但 DHPD1-24 仍然具有通过抑制 MAPK 信号通路抑制 HO 诱导的人晶状体上皮 (HLE) 细胞凋亡的能力。这些结果表明,DHPD1-24 可能是 DHPD1 抑制 HLE 细胞凋亡所需的核心结构域。甲基化分析表明,DHPD1-24 由(1→5)-连接的阿拉伯呋喃糖基、(1→3,6)-连接的甘露吡喃糖基、1-连接的葡萄糖基、(1→4)-连接的葡萄糖基、(1→6)-连接的葡萄糖基、(1→4,6)-连接的葡萄糖基、(1→6)-连接的半乳糖基和 1-连接的木糖基组成,摩尔比为 1.06:1.53:2.11:2.04:0.93:0.91:0.36:1.01。此外,通过 NMR 谱对 DHPD1-24 的一级结构特征进行了表征。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验