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用于 COVID-19 刺突蛋白的碳水化合物配体。

Carbohydrate Ligands for COVID-19 Spike Proteins.

机构信息

Department of Medical Laboratory Science and Biotechnology, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

Institute of Basic Medical Science, College of Medicine, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

Viruses. 2022 Feb 6;14(2):330. doi: 10.3390/v14020330.

Abstract

An outbreak of SARS-CoV-2 coronavirus (COVID-19) first detected in Wuhan, China, has created a public health emergency all over the world. The pandemic has caused more than 340 million confirmed cases and 5.57 million deaths as of 23 January 2022. Although carbohydrates have been found to play a role in coronavirus binding and infection, the role of cell surface glycans in SARS-CoV-2 infection and pathogenesis is still not understood. Herein, we report that the SARS-CoV-2 spike protein S1 subunit binds specifically to blood group A and B antigens, and that the spike protein S2 subunit has a binding preference for Le antigens. Further examination of the binding preference for different types of red blood cells (RBCs) indicated that the spike protein S1 subunit preferentially binds with blood group A RBCs, whereas the spike protein S2 subunit prefers to interact with blood group Le RBCs. Angiotensin converting enzyme 2 (ACE2), a known target of SARS-CoV-2 spike proteins, was identified to be a blood group A antigen-containing glycoprotein. Additionally, 6-sulfo -acetyllactosamine was found to inhibit the binding of the spike protein S1 subunit with blood group A RBCs and reduce the interaction between the spike protein S1 subunit and ACE2.

摘要

一种在中国武汉首次发现的 SARS-CoV-2 冠状病毒(COVID-19)引发了全球公共卫生紧急事件。截至 2022 年 1 月 23 日,大流行已导致超过 3.4 亿例确诊病例和 557 万人死亡。尽管已经发现碳水化合物在冠状病毒结合和感染中起作用,但细胞表面糖在 SARS-CoV-2 感染和发病机制中的作用仍不清楚。在此,我们报告 SARS-CoV-2 刺突蛋白 S1 亚基特异性结合血型 A 和 B 抗原,刺突蛋白 S2 亚基对 Le 抗原具有结合偏好。进一步研究不同类型红细胞(RBC)的结合偏好表明,刺突蛋白 S1 亚基优先与血型 A RBC 结合,而刺突蛋白 S2 亚基更喜欢与血型 Le RBC 相互作用。血管紧张素转换酶 2(ACE2)是 SARS-CoV-2 刺突蛋白的已知靶标,被鉴定为含有血型 A 抗原的糖蛋白。此外,发现 6-硫酸乙酰乳糖胺抑制了刺突蛋白 S1 亚基与血型 A RBC 的结合,并减少了刺突蛋白 S1 亚基与 ACE2 的相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a0e/8880561/ee1a2db65e6a/viruses-14-00330-g001.jpg

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