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东当归多糖的研究——IV. 北川东当归根中一种抗补体阿拉伯半乳聚糖的特性

Studies on polysaccharides from Angelica acutiloba--IV. Characterization of an anti-complementary arabinogalactan from the roots of Angelica acutiloba Kitagawa.

作者信息

Yamada H, Kiyohara H, Cyong J C, Otsuka Y

出版信息

Mol Immunol. 1985 Mar;22(3):295-304. doi: 10.1016/0161-5890(85)90165-8.

Abstract

An anti-complementary polysaccharide, AR-arabinogalactan, was isolated from the roots of Angelica acutiloba Kitagawa (Japanese name = Yamato-Tohki), and purified by chromatography on DEAE-Sephadex A-50, Sephadex G-100, Sepharose CL-2B and concanavalin A-Sepharose. AR-arabinogalactan was composed of arabinose and galactose in a molar ratio of 1.2:1.0 and a small amount of galacturonic acid. The results of methylation and exo-alpha-L-arabinofuranosidase treatment showed that the polysaccharide was a branched arabinogalactan containing a backbone involving galactopyranosyl (1----6) linkages. Most of the arabinose was present as an alpha-L-furanosyl residue in the non-reducing terminals and side chains. The (1----3)-linked galactopyranosyl residue might be linked to the arabinosyl side chains. alpha-L-arabinofuranosidase digestion did not destroy the anti-complementary activity of the polysaccharide. After incubation of the serum with AR-arabinogalactan in the absence of Ca2+ ions, a cleavage of C3 in the serum was detected by immunoelectrophoresis as well as from the consumption of complement when rabbit erythrocytes were used in the assay system. A marked consumption of C4 was also observed to have occurred when serum was incubated with AR-arabinogalactan in the presence of Ca2+ ions. Collectively considered these results indicate that the mode of complement activation by AR-arabinogalactan is via both the alternative and the classical pathway.

摘要

从当归(日语名=大和东机)的根部分离出一种抗补体多糖AR-阿拉伯半乳聚糖,并通过DEAE-葡聚糖A-50、葡聚糖G-100、琼脂糖CL-2B和伴刀豆球蛋白A-琼脂糖进行色谱纯化。AR-阿拉伯半乳聚糖由阿拉伯糖和半乳糖组成,摩尔比为1.2:1.0,还含有少量半乳糖醛酸。甲基化和外切-α-L-阿拉伯呋喃糖苷酶处理结果表明,该多糖是一种支链阿拉伯半乳聚糖,其主链包含吡喃半乳糖基(1→6)键。大部分阿拉伯糖以α-L-呋喃糖基残基的形式存在于非还原末端和侧链中。(1→3)连接的吡喃半乳糖基残基可能与阿拉伯糖基侧链相连。α-L-阿拉伯呋喃糖苷酶消化不会破坏多糖的抗补体活性。在无Ca2+离子的情况下,将血清与AR-阿拉伯半乳聚糖孵育后,通过免疫电泳检测到血清中C3的裂解,并且在检测系统中使用兔红细胞时,也可从补体的消耗情况看出。当血清在有Ca2+离子的情况下与AR-阿拉伯半乳聚糖孵育时,还观察到C4有明显消耗。综合考虑这些结果表明,AR-阿拉伯半乳聚糖激活补体的方式是通过替代途径和经典途径。

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