Suppr超能文献

单分子成像揭示宿主唾液酸对新冠病毒刺突受体结合域的变构刺激作用。

Single-molecule imaging reveals allosteric stimulation of SARS-CoV-2 spike receptor binding domain by host sialic acid.

作者信息

Díaz-Salinas Marco A, Jain Aastha, Durham Natasha D, Munro James B

机构信息

Department of Microbiology and Physiological Systems, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.

Department of Biochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.

出版信息

Sci Adv. 2024 Jul 19;10(29):eadk4920. doi: 10.1126/sciadv.adk4920. Epub 2024 Jul 17.

Abstract

Conformational dynamics of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike glycoprotein (S) mediate exposure of the binding site for the cellular receptor, angiotensin-converting enzyme 2 (ACE2). The N-terminal domain (NTD) of S binds terminal sialic acid (SA) moieties on the cell surface, but the functional role of this interaction in virus entry is unknown. Here, we report that NTD-SA interaction enhances both S-mediated virus attachment and ACE2 binding. Through single-molecule Förster resonance energy transfer imaging of individual S trimers, we demonstrate that SA binding to the NTD allosterically shifts the S conformational equilibrium, favoring enhanced exposure of the ACE2-binding site. Antibodies that target the NTD block SA binding, which contributes to their mechanism of neutralization. These findings inform on mechanisms of S activation at the cell surface.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突糖蛋白(S)的构象动力学介导细胞受体血管紧张素转换酶2(ACE2)结合位点的暴露。S的N端结构域(NTD)与细胞表面的末端唾液酸(SA)部分结合,但其在病毒进入中的功能作用尚不清楚。在这里,我们报告NTD-SA相互作用增强了S介导的病毒附着和ACE2结合。通过对单个S三聚体进行单分子Förster共振能量转移成像,我们证明SA与NTD的结合通过变构改变S的构象平衡,有利于增强ACE2结合位点的暴露。靶向NTD的抗体可阻断SA结合,这有助于其发挥中和作用的机制。这些发现为S在细胞表面的激活机制提供了信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f986/466946/cb0f12ec8a2b/sciadv.adk4920-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验