Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK.
BioPharmaSpec Inc, 363 Phoenixville Pike, Malvern, PA 19355, USA.
Glycobiology. 2021 Apr 1;31(3):181-187. doi: 10.1093/glycob/cwaa085.
The novel coronavirus SARS-CoV-2, the infective agent causing COVID-19, is having a global impact both in terms of human disease as well as socially and economically. Its heavily glycosylated spike glycoprotein is fundamental for the infection process, via its receptor-binding domains interaction with the glycoprotein angiotensin-converting enzyme 2 on human cell surfaces. We therefore utilized an integrated glycomic and glycoproteomic analytical strategy to characterize both N- and O- glycan site-specific glycosylation within the receptor-binding domain. We demonstrate the presence of complex-type N-glycans with unusual fucosylated LacdiNAc at both sites N331 and N343 and a single site of O-glycosylation on T323.
新型冠状病毒 SARS-CoV-2 是引起 COVID-19 的病原体,它在人类疾病以及社会和经济方面都产生了全球性的影响。其高度糖基化的刺突糖蛋白对于感染过程至关重要,通过其受体结合域与人类细胞表面的血管紧张素转换酶 2 的相互作用。因此,我们利用一种综合的糖组学和糖蛋白质组学分析策略来描述受体结合域中 N-和 O-糖基化位点特异性糖基化。我们证明了在 N331 和 N343 两个位点以及 T323 上存在单个 O-糖基化位点的复杂型 N-聚糖,并且具有异常岩藻糖基化的 LacdiNAc。