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作 者:Ping Li Zheng Li Dawei Zhang Qiong Jia
机构地区:[1]College of Chemistry,Jilin University,Changchun 130012,China [2]Key Laboratory for Molecular Enzymology and Engineering of Ministry of Education,College of Life Sciences,Jilin University,Changchun 130012,China
出 处:《Chinese Chemical Letters》2023年第3期283-287,共5页中国化学快报(英文版)
基 金:financially supported by the Fundamental Research Funds for the Central Universities, Jilin University, China。
摘 要:β-Cyclodextrin(β-CD) based materials have attracted great attention in the separation of hydrophilic glycopeptides due to the abundant hydroxyl groups in its exterior. However, the current materials based on β-CD generally has complex synthesis process and harsh experimental conditions, on the other hand,the interior cavity of β-CD is hydrophobic and is harmful to capture glycopeptides. Herein, a novel hydrophilic material based on β-CD was engineered via a self-assembly process utilizing L-cysteine(L-Cys)or glutathione(GSH) derived adamantane for highly efficient glycopeptide enrichment. It is the first attempt to make use of the hydrophobic interior cavity of β-CD for hydrophilic glycopeptide capture. Taking advantages of strong hydrophilicity and superparamagnetism, the as-prepared materials possess low detection limit, high selectively, and excellent reusability when employed to glycopeptide enrichment. In addition, the feasibility of the hydrophilic material based on β-CD was verified by enriching glycopeptides from human serum and saliva samples. This study provides a heuristic strategy for the application of β-CD-based self-assembly materials in the enrichment of glycopeptides. Importantly, this strategy certified a possible that the change of glycopeptide enrichment sites through host-guest interaction between β-CD and adamantane derivatives with different functional groups.
关 键 词:Β-CYCLODEXTRIN HYDROPHILIC SELF-ASSEMBLY ENRICHMENT GLYCOPEPTIDES
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