TY - JOUR
T1 - SARS-CoV-2 Nsp3 unique domain SUD interacts with guanine quadruplexes and G4-ligands inhibit this interaction
AU - Lavigne, Marc
AU - Helynck, Olivier
AU - Rigolet, Pascal
AU - Boudria-Souilah, Rofia
AU - Nowakowski, Mireille
AU - Baron, Bruno
AU - Brülé, Sébastien
AU - Hoos, Sylviane
AU - Raynal, Bertrand
AU - Guittat, Lionel
AU - Beauvineau, Claire
AU - Petres, Stéphane
AU - Granzhan, Anton
AU - Guillon, Jean
AU - Pratviel, Geneviève
AU - Teulade-Fichou, Marie Paule
AU - England, Patrick
AU - Mergny, Jean Louis
AU - Munier-Lehmann, Hélène
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.
PY - 2021/7/21
Y1 - 2021/7/21
N2 - The multidomain non-structural protein 3 (Nsp3) is the largest protein encoded by coronavirus (CoV) genomes and several regions of this protein are essential for viral replication. Of note, SARS-CoV Nsp3 contains a SARS-Unique Domain (SUD), which can bind Guanine-rich non-canonical nucleic acid structures called G-quadruplexes (G4) and is essential for SARS-CoV replication. We show herein that the SARS-CoV-2 Nsp3 protein also contains a SUD domain that interacts with G4s. Indeed, interactions between SUD proteins and both DNA and RNA G4s were evidenced by G4 pull-down, Surface Plasmon Resonance and Homogenous Time Resolved Fluorescence. These interactions can be disrupted by mutations that prevent oligonucleotides from folding into G4 structures and, interestingly, by molecules known as specific ligands of these G4s. Structural models for these interactions are proposed and reveal significant differences with the crystallographic and modeled 3D structures of the SARS-CoV SUD-NM/G4 interaction. Altogether, our results pave the way for further studies on the role of SUD/G4 interactions during SARS-CoV-2 replication and the use of inhibitors of these interactions as potential antiviral compounds.
AB - The multidomain non-structural protein 3 (Nsp3) is the largest protein encoded by coronavirus (CoV) genomes and several regions of this protein are essential for viral replication. Of note, SARS-CoV Nsp3 contains a SARS-Unique Domain (SUD), which can bind Guanine-rich non-canonical nucleic acid structures called G-quadruplexes (G4) and is essential for SARS-CoV replication. We show herein that the SARS-CoV-2 Nsp3 protein also contains a SUD domain that interacts with G4s. Indeed, interactions between SUD proteins and both DNA and RNA G4s were evidenced by G4 pull-down, Surface Plasmon Resonance and Homogenous Time Resolved Fluorescence. These interactions can be disrupted by mutations that prevent oligonucleotides from folding into G4 structures and, interestingly, by molecules known as specific ligands of these G4s. Structural models for these interactions are proposed and reveal significant differences with the crystallographic and modeled 3D structures of the SARS-CoV SUD-NM/G4 interaction. Altogether, our results pave the way for further studies on the role of SUD/G4 interactions during SARS-CoV-2 replication and the use of inhibitors of these interactions as potential antiviral compounds.
U2 - 10.1093/nar/gkab571
DO - 10.1093/nar/gkab571
M3 - Article
C2 - 34232992
AN - SCOPUS:85112126872
SN - 0305-1048
VL - 49
SP - 7695
EP - 7712
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 13
ER -