化学
糖苷键
替代补体途径
多糖
补体系统
立体化学
经典补体途径
摩尔比
凝集素途径
生物化学
酶
抗体
生物
催化作用
免疫学
作者
Zhengyu Hu,Jiaming Wang,Long Jin,Yuanqi Duan,Xiaohui Zhang,Jinfeng Sun,Wei Zhou,Gao Li
标识
DOI:10.1002/cbdv.202200294
摘要
Abstract The two novel polysaccharides, DMP‐1 and DMP‐2, with molecular weights of 4.1553×10 5 kDa and 1.9764×10 5 kDa, respectively, were isolated from Dracocephalum moldavica . The structural characterization indicated that DMP‐1 and DMP‐2 shared a similar backbone consisting of →5)‐Ara f ‐(1→, Man p ‐(1→, Glc p ‐(1→, →2)‐Man p ‐(1→, →6)‐Glc p ‐(1→ and →3,6)‐Gal p ‐(1→ with a different molar ratios and triple‐helix structures with α ‐ and β ‐type glycosidic bonds. The anti‐complementary activity evaluation showed that DMP‐1 and DMP‐2 had strong complement inhibition through the classical pathway (CP), alternative pathway (AP) and lectin pathway (LP). Mechanistic studies indicated that DMP‐1 can block the activation cascade of the complement system by targeting C2, C3, C5, C9, Factor B and Factor P, and that DMP‐2 inhibited complement activation by blocking C2, C3, C4, C5, C9 and Factor B.
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