7OPL

CryoEM structure of DNA Polymerase alpha - primase bound to SARS CoV nsp1

7OPL の概要

• エントリーDOI: 10.2210/pdb7opl/pdb
• EMDBエントリー: 13020
• 分子名称: DNA polymerase alpha catalytic subunit, DNA polymerase alpha subunit B, DNA primase small subunit, ... (7 entities in total)
• 機能のキーワード: dna polymerase, primase, viral protein, dna binding protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 308543.43

構造登録者

Kilkenny, M.L.,Pellegrini, L. (登録日: 2021-06-01, 公開日: 2021-11-10, 最終更新日: 2024-07-17)

主引用文献

Kilkenny, M.L.,Veale, C.E.,Guppy, A.,Hardwick, S.W.,Chirgadze, D.Y.,Rzechorzek, N.J.,Maman, J.D.,Pellegrini, L.
Structural basis for the interaction of SARS-CoV-2 virulence factor nsp1 with DNA polymerase alpha-primase.
Protein Sci., 31:333-344, 2022

PubMed Abstract: The molecular mechanisms that drive the infection by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-the causative agent of coronavirus disease 2019 (COVID-19)-are under intense current scrutiny to understand how the virus operates and to uncover ways in which the disease can be prevented or alleviated. Recent proteomic screens of the interactions between viral and host proteins have identified the human proteins targeted by SARS-CoV-2. The DNA polymerase α (Pol α)-primase complex or primosome-responsible for initiating DNA synthesis during genomic duplication-was identified as a target of nonstructural protein 1 (nsp1), a major virulence factor in the SARS-CoV-2 infection. Here, we validate the published reports of the interaction of nsp1 with the primosome by demonstrating direct binding with purified recombinant components and providing a biochemical characterization of their interaction. Furthermore, we provide a structural basis for the interaction by elucidating the cryo-electron microscopy structure of nsp1 bound to the primosome. Our findings provide biochemical evidence for the reported targeting of Pol α by the virulence factor nsp1 and suggest that SARS-CoV-2 interferes with Pol α's putative role in the immune response during the viral infection.

PubMed: 34719824
DOI: 10.1002/pro.4220

実験手法

ELECTRON MICROSCOPY (4.12 Å)