Development of zirconium modified adenosine triphosphate functionalized monolith for specific enrichment of N-glycans

被引:4
|
作者
Shao, Huikai [1 ,2 ,3 ,4 ,5 ]
Lai, Liang [1 ,2 ,3 ]
Xu, Dongsheng [1 ,2 ,3 ]
Crommen, Jacques [1 ,6 ]
Wang, Qiqin [1 ,2 ,3 ]
Jiang, Zhengjin [1 ,2 ,3 ]
机构
[1] Jinan Univ, Coll Pharm, Inst Pharmaceut Anal, Guangzhou 510632, Peoples R China
[2] Jinan Univ, Dept Pharm, Guangzhou 510632, Peoples R China
[3] Jinan Univ, Guangdong Prov Key Lab Pharmacodynam Constituents, Guangzhou 510632, Peoples R China
[4] Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Dept Pharm, Chengdu 610072, Peoples R China
[5] Univ Elect Sci & Technol China, Sch Med, Personalized Drug Therapy Key Lab Sichuan Prov, Chengdu 610072, Peoples R China
[6] Univ Liege, Ctr Interdisciplinary Res Med CIRM, Lab Anal Med, Quartier Hop,Ave Hippocrate 15, B-4000 Liege, Belgium
基金
中国国家自然科学基金;
关键词
Adenosine triphosphate; Zr(IV)-ATP functionalized monolith; N-glycans; Immobilized metal affinity chromatography; METAL AFFINITY-CHROMATOGRAPHY; SELECTIVE ENRICHMENT; POLYMERIC MONOLITHS; FACILE PREPARATION; PHOSPHATE; COLUMN; OLIGOSACCHARIDES; METHACRYLATE; SEPARATION;
D O I
10.1016/j.chroma.2021.462090
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, to selectively enrich N-glycans from complex biological samples, a novel Zr(IV) mod-ified adenosine triphosphate (Zr(IV)-ATP) functionalized monolith was prepared through a facile ap-proach. Well-defined macroporous structure was observed in the ATP functionalized monolith, which allows rapid mass transfer under low backpressure and is beneficial for the enrichment of N-glycans. After being modified with Zr(IV), the resulting Zr(IV)-ATP functionalized monolith could selectively capture N-glycans through the specific interactions between the sulfonate groups of 1-aminopyrene-3,6,8-trisulfonic acid (APTS) labeled N-glycans and Zr(IV). An APTS labeled maltooligosaccharide lad -der was used to optimize the enrichment conditions for APTS labeled N-glycans, and capillary elec-trophoresis (CE) coupled with laser-induced fluorescence (LIF) detector was employed to evaluate the enrichment efficiency. The results show that the APTS labeled maltooligosaccharides could be en-riched under the selected conditions and the signal amplify factors of the maltooligosaccharides were between 7.4 and 19.5 with RSDs for reproducibility from 4.0% to 8.3% (n = 3). Finally, the pro-posed method was successfully used for the enrichment and detection of N-glycans released from Ribonuclease B. (c) 2021 Elsevier B.V. All rights reserved.
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收藏
页数:8
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