多效蛋白
米德金
化学
表面等离子共振
硫酸软骨素
生物化学
糖胺聚糖
硫酸乙酰肝素
低聚糖
糖复合物
立体化学
生长因子
受体
纳米技术
纳米颗粒
材料科学
作者
Shuang Yang,Guangyan Zhang,Jin-Yue Zhang,Tianqi Li,Zhehui Zhao,Yinghong Wang,Pingsheng Lei
标识
DOI:10.1080/10286020.2022.2146583
摘要
A total synthesis approach of CS-E oligosaccharides was established and a series of derivatives were synthesized. These oligosaccharides were evaluated for a glycosaminoglycan (GAG)-binding protein interaction against cytokines, midkine, and pleiotrophin, by surface-plasmon resonance (SPR) assay. The binding epitopes of oligosaccharides to midkine were mapped using a saturation transfer difference (STD) NMR technique. The groups on the reducing end contributed to binding affinity, and should not be ignored in biological assays. These findings contribute to the structure and activity relationship research and a foundation of understanding that will underpin potential future optimization of this class of oligosaccharides as pharmaceutical agents.
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