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基于核磁共振的新冠病毒Nsp9纳米抗体分析揭示了一种针对新冠肺炎的可能抗病毒策略。

NMR-Based Analysis of Nanobodies to SARS-CoV-2 Nsp9 Reveals a Possible Antiviral Strategy Against COVID-19.

作者信息

Esposito Gennaro, Hunashal Yamanappa, Percipalle Mathias, Venit Tomas, Dieng Mame Massar, Fogolari Federico, Hassanzadeh Gholamreza, Piano Fabio, Gunsalus Kristin C, Idaghdour Youssef, Percipalle Piergiorgio

机构信息

Chemistry Program, Science Division, New York University Abu Dhabi, Abu Dhabi, 129188, United Arab Emirates.

Istituto Nazionale Biostrutture e Biosistemi, Roma, 00136, Italy.

出版信息

Adv Biol (Weinh). 2021 Dec;5(12):e2101113. doi: 10.1002/adbi.202101113. Epub 2021 Oct 27.

Abstract

Following the entry into the host cell, SARS-CoV-2 replication is mediated by the replication transcription complex (RTC) assembled through a number of nonstructural proteins (Nsps). A monomeric form of Nsp9 is particularly important for RTC assembly and function. In the present study, 136 unique nanobodies targeting Nsp9 are generated. Several nanobodies belonging to different B-cell lineages are expressed, purified, and characterized. Results from immunoassays applied to purified Nsp9 and neat saliva from coronavirus disease (COVID-19) patients show that these nanobodies effectively and specifically recognize both recombinant and endogenous Nsp9. Nuclear magnetic resonance analyses supported by molecular dynamics reveal a composite Nsp9 oligomerization pattern and demonstrate that both nanobodies stabilize the tetrameric form of wild-type Nsp9 also identifying the epitopes on the tetrameric assembly. These results can have important implications in the potential use of these nanobodies to combat viral replication.

摘要

进入宿主细胞后,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的复制由通过多种非结构蛋白(Nsps)组装而成的复制转录复合体(RTC)介导。Nsp9的单体形式对RTC的组装和功能尤为重要。在本研究中,生成了136种靶向Nsp9的独特纳米抗体。表达、纯化并表征了几种属于不同B细胞谱系的纳米抗体。应用于纯化的Nsp9和冠状病毒病(COVID-19)患者纯唾液的免疫分析结果表明,这些纳米抗体能有效且特异性地识别重组Nsp9和内源性Nsp9。分子动力学支持的核磁共振分析揭示了复合Nsp9寡聚化模式,并证明这两种纳米抗体均能稳定野生型Nsp9的四聚体形式,同时也确定了四聚体组装体上的表位。这些结果对于这些纳米抗体在对抗病毒复制方面的潜在应用可能具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb2/8646926/08a1cb4a21c7/ADBI-5-2101113-g003.jpg

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