Recognition of urinary N-linked glycopeptides in kidney cancer patients by hydrophilic carbohydrate functionalized magnetic metal organic framework combined with LC-MS/MS

被引:26
作者
Hu, Xufang [1 ]
Wu, Yonglei [1 ]
Deng, Chunhui [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Inst Biomed Sci, Dept Chem,Dept Gastroenterol & Hepatol, Shanghai 200433, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Glycosylation; Post-translational modification; Human urine; Magnetic nanomaterials; Post-functionalization; ENRICHMENT; GLYCOSYLATION; NANOPARTICLES; BIOMARKER; CHEMISTRY; ACID;
D O I
10.1007/s00604-020-04595-y
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A hydrophilic carbohydrate functionalized magnetic metal organic framework (Mag Zr-MOF@G6P) was synthesized via a facile one-step modification strategy for selective glycopeptide capture in virtue of hydrophilic interaction chromatography technique. The inherently hydrophilic Zr-MOF layer not only provides selective size-sieving pore structures but also offers large specific surface area to afford abundant affinity sites. Hydroxyl-rich glucose-6-phosphate was immobilized onto the Zr-MOF via a straightforward coordination manner to regulate its surface property, for the purpose of enhancing its hydrophilicity. Benefitting from the merits of Zr-MOF and glucose-6-phosphate, the as-designed composite exhibits good selectivity (the mass ratio of HRP digests to BSA digests was up to1:200) and low limit of detection (0.1 fmol mu L-1) towards the recognition of glycopeptides from standard samples. More excitingly, glycopeptides in urine of healthy people and patients with kidney cancer were successfully enriched and identified by the combined liquid chromatography-mass spectrometry/mass spectrometry technology (LC-MS/MS). Further gene ontology analysis of molecular function and biological process revealed that 13 original glycoproteins of the identified glycopeptides from urine of patients significantly participate in diverse cancer-associated events, including collagen binding, immunoglobulin receptor binding, antigen binding, and complement activation process.
引用
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页数:12
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