Suppr超能文献

一种抗体的表位,该抗体在刺突蛋白的保守结构域 1 中中和广泛的 SARS-CoV-2 变体。

Epitopes of an antibody that neutralizes a wide range of SARS-CoV-2 variants in a conserved subdomain 1 of the spike protein.

机构信息

Division of Clinical Virology, Center for Infectious Diseases, Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan.

Structural Biology Division, Japan Synchrotron Radiation Research Institute SPring-8, Sayo, Hyogo, Japan.

出版信息

J Virol. 2024 May 14;98(5):e0041624. doi: 10.1128/jvi.00416-24. Epub 2024 Apr 16.

Abstract

The evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has continued, enabling the virus to escape from host immunity by changing its spike antigen, while biased toward the receptor-binding domain and N-terminal domain. Here, we isolated a novel pan-SARS-CoV-2 neutralizing antibody (which we named MO11) for even the recent dominators XBB.1.16 and EG.5.1, from a convalescent patient who had received three doses of an original mRNA COVID-19 vaccination. A cryo-electron microscopy analysis of the spike-MO11 complex at 2.3 Å atomic resolution revealed that it recognizes a conserved epitope hidden behind a glycan shield at N331 on subdomain 1 (SD1), holding both the N- and C-terminal segments comprising SD1. Our identification of MO11 unveiled the functional importance of SD1 for the spike's function, and we discuss the potential availability of a novel common epitope among the SARS-CoV-2 variants.IMPORTANCENovel severe acute respiratory syndrome coronavirus 2 variants with immune evasion ability are still repeatedly emerging, nonetheless, a part of immunity developed in responding to the antigen of earlier variants retains efficacy against recent variants irrespective of the numerous mutations. In exploration for the broadly effective antibodies, we identified a cross-neutralizing antibody, named MO11, from the B cells of the convalescent patient. MO11 targets a novel epitope in subdomain 1 (SD1) and was effective against all emerging variants including XBB.1.16 and EG.5.1. The neutralizing activity covering from D614G to EG.5.1 variants was explained by the conservation of the epitope, and it revealed the importance of the subdomain on regulating the function of the antigen for viral infection. Demonstrated identification of the neutralizing antibody that recognizes a conserved epitope implies basal contribution of such group of antibodies for prophylaxis against COVID-19.

摘要

严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 的进化仍在继续,病毒通过改变其刺突抗原来逃避宿主免疫,同时偏向于受体结合域和 N 端结构域。在这里,我们从一名接受过三剂原始 mRNA COVID-19 疫苗接种的康复患者中分离出一种新型泛 SARS-CoV-2 中和抗体(我们将其命名为 MO11),该抗体甚至可以中和最近的优势株 XBB.1.16 和 EG.5.1。通过对 2.3 Å 原子分辨率的 Spike-MO11 复合物的冷冻电子显微镜分析,发现它识别出一个隐藏在 N 端结构域 1 (SD1) 上 N331 糖基化盾牌后面的保守表位,该表位结合了包括 SD1 的 N 端和 C 端片段。我们对 MO11 的鉴定揭示了 SD1 对 Spike 功能的重要性,我们讨论了 SARS-CoV-2 变体之间可能存在的新型共同表位。

严重急性呼吸综合征冠状病毒 2 的新型变体具有免疫逃逸能力,仍在不断出现,但针对早期变体抗原产生的部分免疫对最近的变体仍然有效,无论突变数量众多。在探索广泛有效的抗体时,我们从康复患者的 B 细胞中鉴定出一种中和抗体,命名为 MO11。MO11 靶向 SD1 中的一个新表位,对所有新兴变体均有效,包括 XBB.1.16 和 EG.5.1。对从 D614G 到 EG.5.1 变体的中和活性的解释是基于该表位的保守性,它揭示了亚结构域在调节抗原功能以进行病毒感染方面的重要性。该中和抗体识别保守表位的鉴定表明,这类抗体对 COVID-19 的预防具有基础性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4ef/11092320/38458a69a4c4/jvi.00416-24.f001.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