Differential analysis of core-fucosylated glycoproteomics enabled by single-step truncation of N-glycans

被引:3
作者
Min, Yao [1 ,3 ]
Wu, Jianhui [2 ]
Hou, Wenhao [3 ]
Li, Xiaoyu [3 ]
Zhao, Xinyuan [3 ]
Guan, Xiaoya [2 ]
Qian, Xiaohong [3 ]
Hao, Chunyi [2 ]
Ying, Wantao [1 ,3 ]
机构
[1] Anhui Med Univ, Sch Basic Med Sci, Hefei 230032, Peoples R China
[2] Peking Univ Canc Hosp & Inst, Minist Educ Beijing, Dept Hepatopancreato Biliary Surg, Key Lab Carcinogenesis & Translat Res, Beijing 102206, Peoples R China
[3] Natl Ctr Prot Sci Beijing, Beijing Proteome Res Ctr, State Key Lab Prote, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
Core fucosylation; Glycoproteome; Mass spectrometry; Pancreatic ductal adenocarcinoma; Endo F3; LARGE-SCALE IDENTIFICATION; INTACT GLYCOPEPTIDES; CANCER; GLYCOSYLATION; PROTEIN; STRATEGY; SURVIVAL; CADHERIN; PRECISE; SITES;
D O I
10.1007/s10719-023-10130-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alpha-1,6 fucosylation of N-glycans (core fucosylation, CF) represents a unique form of N-glycans and is widely involved in disease progression. In order to accurately identify CF glycoproteins, several approaches have been developed based on sequential cleavage with different glycosidases to truncate the N-glycans. Since multi-step sample treatments may introduce quantitation bias and affect the practicality of these approaches in large-scale applications. Here, we systematically evaluated the performance of the single-step treatment of intact glycopeptides by endoglycosidase F3 for CF glycoproteome. The single-step truncation (SST) strategy demonstrated higher quantitative stability and higher efficiency compared with previous approaches. The strategy was further practiced on both cell lines and serum samples. The dysregulation of CF glycopeptides between preoperative and postoperative serum from patients with pancreatic ductal adenocarcinoma was revealed, and the CF modifications of BCHE_N369, CDH5_N112 and SERPIND1_N49 were found to be potential prognostic markers. This study thus provides an efficient solution for large-scale quantitative analysis of the CF glycoproteome.
引用
收藏
页码:541 / 549
页数:9
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