Mass Spectrometry Analysis of SARS-CoV-2 Nucleocapsid Protein Reveals Camouflaging Glycans and Unique Post-Translational Modifications

被引:13
|
作者
Sun, Zeyu [1 ]
Zheng, Xiaoqin [1 ]
Ji, Feiyang [1 ]
Zhou, Menghao [1 ]
Su, Xiaoling [1 ]
Ren, Keyi [1 ]
Li, Lanjuan [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1,Collaborat Innovat Ctr Diag & T, Natl Clin Res Ctr Infect Dis,State Key Lab Diag &, Hangzhou, Zhejiang, Peoples R China
来源
INFECTIOUS MICROBES & DISEASES | 2021年 / 3卷 / 03期
基金
中国国家自然科学基金;
关键词
glycosylation; mass spectrometry; nucleocapsid protein; post-translational modification; SARS-CoV-2; SPIKE GLYCOPROTEIN; SARS-CORONAVIRUS; CLINICAL CHARACTERISTICS; GLYCOSYLATION; INFECTIVITY; ANTIBODY; BINDING; IMMUNOASSAY; INTEGRATION; 2019-NCOV;
D O I
10.1097/IM9.0000000000000071
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The devastating coronavirus disease 2019 (COVID-19) pandemic has prompted worldwide efforts to study structural biological traits of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its viral components. Compared to the Spike protein, which is the primary target for currently available vaccines or antibodies, knowledge about other virion structural components is incomplete. Using high-resolution mass spectrometry, we report a comprehensive post-translational modification (PTM) analysis of nucleocapsid phosphoprotein (NCP), the most abundant structural component of the SARS-CoV-2 virion. In addition to phosphoryl groups, we show that the SARS-CoV-2 NCP is decorated with a variety of PTMs, including N-glycans and ubiquitin. Based on newly identified PTMs, refined protein structural models of SARS-CoV-2 NCP were proposed and potential immune recognition epitopes of NCP were aligned with PTMs. These data can facilitate the design of novel vaccines or therapeutics targeting NCP, as valuable alternatives to the current vaccination and treatment paradigm that is under threat of the ever-mutating SARS-CoV-2 Spike protein.
引用
收藏
页码:149 / 157
页数:9
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