7K5I

SARS-COV-2 nsp1 in complex with human 40S ribosome

7K5I の概要

• エントリーDOI: 10.2210/pdb7k5i/pdb
• EMDBエントリー: 22681
• 分子名称: 40S ribosomal protein S17, 40S ribosomal protein S18, 40S ribosomal protein S19, ... (38 entities in total)
• 機能のキーワード: nsp1, 40s, ribosome-viral protein complex, ribosome/viral protein
• 由来する生物種: Severe acute respiratory syndrome coronavirus 2 (2019-nCoV); 詳細
• タンパク質・核酸の鎖数: 36
• 化学式量合計: 1242944.39

構造登録者

Wang, L.,Shi, M.,Wu, H. (登録日: 2020-09-16, 公開日: 2020-10-14, 最終更新日: 2024-10-09)

主引用文献

Shi, M.,Wang, L.,Fontana, P.,Vora, S.,Zhang, Y.,Fu, T.M.,Lieberman, J.,Wu, H.
SARS-CoV-2 Nsp1 suppresses host but not viral translation through a bipartite mechanism.
Biorxiv, 2020

PubMed Abstract: The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a highly contagious virus that underlies the current COVID-19 pandemic. SARS-CoV-2 is thought to disable various features of host immunity and cellular defense. The SARS-CoV-2 nonstructural protein 1 (Nsp1) is known to inhibit host protein translation and could be a target for antiviral therapy against COVID-19. However, how SARS-CoV-2 circumvents this translational blockage for the production of its own proteins is an open question. Here, we report a bipartite mechanism of SARS-CoV-2 Nsp1 which operates by: (1) hijacking the host ribosome via direct interaction of its C-terminal domain (CT) with the 40S ribosomal subunit and (2) specifically lifting this inhibition for SARS-CoV-2 via a direct interaction of its N-terminal domain (NT) with the 5' untranslated region (5' UTR) of SARS-CoV-2 mRNA. We show that while Nsp1-CT is sufficient for binding to 40S and inhibition of host protein translation, the 5' UTR of SARS-CoV-2 mRNA removes this inhibition by binding to Nsp1-NT, suggesting that the Nsp1-NT-UTR interaction is incompatible with the Nsp1-CT-40S interaction. Indeed, lengthening the linker between Nsp1-NT and Nsp1-CT of Nsp1 progressively reduced the ability of SARS-CoV-2 5' UTR to escape the translational inhibition, supporting that the incompatibility is likely steric in nature. The short SL1 region of the 5' UTR is required for viral mRNA translation in the presence of Nsp1. Thus, our data provide a comprehensive view on how Nsp1 switches infected cells from host mRNA translation to SARS-CoV-2 mRNA translation, and that Nsp1 and 5' UTR may be targeted for anti-COVID-19 therapeutics.

PubMed: 32995777
DOI: 10.1101/2020.09.18.302901

実験手法

ELECTRON MICROSCOPY (2.9 Å)