7THM
SARS-CoV-2 nsp12/7/8 complex with a native N-terminus nsp9
7THM の概要
| エントリーDOI | 10.2210/pdb7thm/pdb |
| EMDBエントリー | 25898 |
| 分子名称 | RNA-directed RNA polymerase, Non-structural protein 8, Non-structural protein 7, ... (7 entities in total) |
| 機能のキーワード | polymerase, niran, capping, nsp9, viral protein |
| 由来する生物種 | Severe acute respiratory syndrome coronavirus 2 (2019-nCoV, SARS-CoV-2) 詳細 |
| タンパク質・核酸の鎖数 | 5 |
| 化学式量合計 | 172588.76 |
| 構造登録者 | Osinski, A.,Tagliabracci, V.S.,Chen, Z.,Li, Y. (登録日: 2022-01-11, 公開日: 2022-03-16, 最終更新日: 2025-05-28) |
| 主引用文献 | Park, G.J.,Osinski, A.,Hernandez, G.,Eitson, J.L.,Majumdar, A.,Tonelli, M.,Henzler-Wildman, K.,Pawlowski, K.,Chen, Z.,Li, Y.,Schoggins, J.W.,Tagliabracci, V.S. The mechanism of RNA capping by SARS-CoV-2. Nature, 609:793-800, 2022 Cited by PubMed Abstract: The RNA genome of SARS-CoV-2 contains a 5' cap that facilitates the translation of viral proteins, protection from exonucleases and evasion of the host immune response. How this cap is made in SARS-CoV-2 is not completely understood. Here we reconstitute the N7- and 2'-O-methylated SARS-CoV-2 RNA cap (GpppA) using virally encoded non-structural proteins (nsps). We show that the kinase-like nidovirus RdRp-associated nucleotidyltransferase (NiRAN) domain of nsp12 transfers the RNA to the amino terminus of nsp9, forming a covalent RNA-protein intermediate (a process termed RNAylation). Subsequently, the NiRAN domain transfers the RNA to GDP, forming the core cap structure GpppA-RNA. The nsp14 and nsp16 methyltransferases then add methyl groups to form functional cap structures. Structural analyses of the replication-transcription complex bound to nsp9 identified key interactions that mediate the capping reaction. Furthermore, we demonstrate in a reverse genetics system that the N terminus of nsp9 and the kinase-like active-site residues in the NiRAN domain are required for successful SARS-CoV-2 replication. Collectively, our results reveal an unconventional mechanism by which SARS-CoV-2 caps its RNA genome, thus exposing a new target in the development of antivirals to treat COVID-19. PubMed: 35944563DOI: 10.1038/s41586-022-05185-z 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.18 Å) |
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