表位
计算生物学
抗原
表位定位
免疫系统
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
抗体
蛋白质结构
生物
病毒学
化学
2019年冠状病毒病(COVID-19)
生物化学
免疫学
医学
传染病(医学专业)
病理
疾病
作者
Michael A. Casasanta,G. M. Jonaid,Liam Kaylor,William Y. Luqiu,Liza‐Anastasia DiCecco,Maria J. Solares,Samantha Berry,W. J. Dearnaley,Deborah F. Kelly
标识
DOI:10.1093/micmic/ozac036
摘要
The nucleocapsid (N) protein is an abundant component of SARS-CoV-2 and a key analyte for lateral-flow rapid antigen tests. Here, we present new structural insights for the SARS-CoV-2 N protein using cryo-electron microscopy (EM) and molecular modeling tools. Epitope mapping based on structural data supported host-immune interactions in the C-terminal portion of the protein, while other regions revealed protein-protein interaction sites. Complementary modeling results suggested that N protein structures from known variants of concern (VOC) are nearly 100% conserved at specific antibody-binding sites. Collectively, these results suggest that rapid tests that target the nucleocapsid C-terminal domain should have similar accuracy across all VOCs. In addition, our combined structural modeling workflow may guide the design of immune therapies to counter viral processes as we plan for future variants and pandemics.
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