Structural characterization and immune activity evaluation of a polysaccharide from Lyophyllum Decastes

水解物 多糖 低聚糖 色谱法 单糖 质谱法 高效液相色谱法 化学 水解 生物化学
作者
Xiaojun Li,Shijun Xiao,Yi Heng Xie,Jiang Chen,Hai-rong Xu,Yuan Yin,Rui Zhang,Tong Yang,Tongyu Zhou,S. Zhang,Pei Hu,Liming Gao,Hui-Ping Peng
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:278: 134628-134628
标识
DOI:10.1016/j.ijbiomac.2024.134628
摘要

An innovative acidic hydrolysate fingerprinting workflow was proposed for the characterization of Lyophyllum Decastes polysaccharide (LDP) by ultra performance liquid chromatography-mass spectrometry (UPLC-MS). The crude polysaccharides were firstly separated and purified by using DE-52 column and the BRT GPC purification system, respectively. The molecular weight and monosaccharide content of homogeneous polysaccharides were ascertained by utilizing HPGPC and ion chromatography separately. Secondly, the linkage of LDP was identified by methylation analysis and 1D/2D NMR spectra. The UPLC-MS/MS was used to scan and identify the acidic hydrolysate products of LDP using the PGC column. The oligosaccharides were collected by chromatography and identified by mass spectrometry. Thirdly, the expression of IL-1β, IL-6, iNOS, TNF-α and IFNAR-I was measured in order to assess the immunological activity of LDP. Besides, the targeted receptors identification of polysaccharides was performed by screening the expression of TLRs family protein. The results showed that oligosaccharide fragments with different molecular weights can be obtained by partial hydrolysis, which further verified that the structures of LDP polysaccharides was a 1-6-linked β-glucan. Moreover, the LDP polysaccharide can up-regulate the content of IL-1β, IL-6, iNOS, TNF-α and IFNAR-I and plays an important immunoregulation role through TLRs family.
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