| Literature DB >> 34341581 |
Jiechen Shen1, Li Jia1, Liuyi Dang1, Yuanjie Su2, Jie Zhang2, Yintai Xu1, Bojing Zhu1, Zexuan Chen1, Jingyu Wu1, Rongxia Lan1, Zhifang Hao1, Chen Ma1, Ting Zhao1, Ni Gao1, Jieyun Bai1, Yuan Zhi1, Jun Li1, Junying Zhang2, Shisheng Sun3.
Abstract
Precision mapping of glycans at structural and site-specific level is still one of the most challenging tasks in the glycobiology field. Here, we describe a modularization strategy for de novo interpretation of N-glycan structures on intact glycopeptides using tandem mass spectrometry. An algorithm named StrucGP is also developed to automate the interpretation process for large-scale analysis. By dividing an N-glycan into three modules and identifying each module using distinct patterns of Y ions or a combination of distinguishable B/Y ions, the method enables determination of detailed glycan structures on thousands of glycosites in mouse brain, which comprise four types of core structure and 17 branch structures with three glycan subtypes. Owing to the database-independent glycan mapping strategy, StrucGP also facilitates the identification of rare/new glycan structures. The approach will be greatly beneficial for in-depth structural and functional study of glycoproteins in the biomedical research.Entities:
Year: 2021 PMID: 34341581 DOI: 10.1038/s41592-021-01209-0
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547