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组合质谱和凝集素微阵列分析揭示了 SARS-CoV-2 祖先株和 γ 变异株病毒衍生 Spike 蛋白的糖基化特征。

Combinatorial Approach with Mass Spectrometry and Lectin Microarray Dissected Site-Specific Glycostem and Glycoleaf Features of the Virion-Derived Spike Protein of Ancestral and γ Variant SARS-CoV-2 Strains.

机构信息

Molecular and Cellular Glycoproteomics Research Group, Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science & Technology, Tsukuba, Ibaraki 305-8565, Japan.

One Health Research Center, Hokkaido University, Sapporo, Hokkaido 060-0818, Japan.

出版信息

J Proteome Res. 2024 Apr 5;23(4):1408-1419. doi: 10.1021/acs.jproteome.3c00874. Epub 2024 Mar 27.

Abstract

The coronavirus disease (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has impacted public health globally. As the glycosylation of viral envelope glycoproteins is strongly associated with their immunogenicity, intensive studies have been conducted on the glycans of the glycoprotein of SARS-CoV-2, the spike (S) protein. Here, we conducted intensive glycoproteomic analyses of the SARS-CoV-2 S protein of ancestral and γ-variant strains using a combinatorial approach with two different technologies: mass spectrometry (MS) and lectin microarrays (LMA). Our unique MS1-based glycoproteomic technique, Glyco-RIDGE, in addition to MS2-based Byonic search, identified 1448 (ancestral strain) and 1785 (γ-variant strain) site-specific glycan compositions, respectively. Asparagine at amino acid position 20 (N20) is mainly glycosylated within two successive potential glycosylation sites, N17 and N20, of the γ-variant S protein; however, we found low-frequency glycosylation at N17. Our novel approaches, glycostem mapping and glycoleaf scoring, also illustrate the moderately branched/extended, highly fucosylated, and less sialylated natures of the glycoforms of S proteins. Subsequent LMA analysis emphasized the intensive end-capping of glycans by Lewis fucoses, which complemented the glycoproteomic features. These results illustrate the high-resolution glycoproteomic features of the SARS-CoV-2 S protein, contributing to vaccine design and understanding of viral protein synthesis.

摘要

新型冠状病毒病(COVID-19)大流行是由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的,对全球公共卫生造成了影响。由于病毒包膜糖蛋白的糖基化与其免疫原性密切相关,因此对 SARS-CoV-2 糖蛋白(刺突(S)蛋白)的聚糖进行了深入研究。在这里,我们使用两种不同技术(质谱(MS)和凝集素微阵列(LMA))的组合方法,对 SARS-CoV-2 的 S 蛋白的原始和γ变体株进行了密集的糖蛋白质组学分析。除了基于 MS2 的 Byonic 搜索外,我们独特的基于 MS1 的糖蛋白质组学技术 Glyco-RIDGE 还分别鉴定出了 1448 个(原始株)和 1785 个(γ变体株)位点特异性糖基化组成。天冬酰胺在氨基酸位置 20(N20)主要在 γ 变体 S 蛋白的两个连续潜在糖基化位点 N17 和 N20 内发生糖基化;然而,我们发现 N17 处存在低频糖基化。我们的新方法糖基干图映射和糖基叶评分也说明了 S 蛋白糖型的中度分支/扩展、高度岩藻糖基化和较少唾液酸化的性质。随后的 LMA 分析强调了 Lewis 岩藻糖对聚糖的强烈末端封闭,这补充了糖蛋白质组学特征。这些结果说明了 SARS-CoV-2 S 蛋白的高分辨率糖蛋白质组学特征,有助于疫苗设计和病毒蛋白合成的理解。

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