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利用 StrucGP 对 COVID-19 病毒刺突进行结构和位点特异性糖基化分析。

Structural- and Site-Specific Glycosylation Characterization of COVID-19 Virus Spike with StrucGP.

机构信息

College of Life Sciences, Northwest University, Xi'an, Shaanxi Province 710069, China.

出版信息

Anal Chem. 2022 Sep 13;94(36):12274-12279. doi: 10.1021/acs.analchem.2c02265. Epub 2022 Aug 29.

Abstract

The spike (S) protein plays a key role in COVID-19 (SARS-CoV-2) infection and host-cell entry. Previous studies have systematically analyzed site-specific glycan compositions as well as many important structural motifs of the S protein. Here, we further provide structural-clear glycosylation of the S protein at a site-specific level by using our recently developed structural- and site-specific glycoproteomics sequencing algorithm, StrucGP. In addition to the common glycans as detected in previous studies, many uncommon glycosylation structures such as LacdiNAc structures, Lewis structures, Mannose 6-phosphate (M6P) residues, and bisected core structures were unambiguously mapped at a total of 20 glycosites in the S protein trimer and protomer. These data further support the glycosylation structural-functional investigations of the COVID-19 virus spike.

摘要

刺突(S)蛋白在 COVID-19(SARS-CoV-2)感染和宿主细胞进入中发挥关键作用。先前的研究已经系统地分析了 S 蛋白的特定糖基组成以及许多重要的结构基序。在这里,我们进一步通过使用我们最近开发的结构和特定位置糖蛋白质组学测序算法 StrucGP,在特定位置水平上提供 S 蛋白的结构清晰的糖基化。除了先前研究中检测到的常见糖基外,许多不常见的糖基化结构,如 LacdiNAc 结构、Lewis 结构、甘露糖 6-磷酸(M6P)残基和双分叉核心结构,在 S 蛋白三聚体和单体中的总共 20 个糖基化位点上被明确映射。这些数据进一步支持 COVID-19 病毒刺突的糖基化结构功能研究。

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