학술논문
SARS-CoV-2 Mpro responds to oxidation by forming disulfide and NOS/SONOS bonds
Document Type
article
Author
Patrick Y. A. Reinke; Robin Schubert; Dominik Oberthür; Marina Galchenkova; Aida Rahmani Mashhour; Sebastian Günther; Anaïs Chretien; Adam Round; Brandon Charles Seychell; Brenna Norton-Baker; Chan Kim; Christina Schmidt; Faisal H. M. Koua; Alexandra Tolstikova; Wiebke Ewert; Gisel Esperanza Peña Murillo; Grant Mills; Henry Kirkwood; Hévila Brognaro; Huijong Han; Jayanath Koliyadu; Joachim Schulz; Johan Bielecki; Julia Lieske; Julia Maracke; Juraj Knoska; Kristina Lorenzen; Lea Brings; Marcin Sikorski; Marco Kloos; Mohammad Vakili; Patrik Vagovic; Philipp Middendorf; Raphael de Wijn; Richard Bean; Romain Letrun; Seonghyun Han; Sven Falke; Tian Geng; Tokushi Sato; Vasundara Srinivasan; Yoonhee Kim; Oleksandr M. Yefanov; Luca Gelisio; Tobias Beck; Andrew S. Doré; Adrian P. Mancuso; Christian Betzel; Saša Bajt; Lars Redecke; Henry N. Chapman; Alke Meents; Dušan Turk; Winfried Hinrichs; Thomas J. Lane
Source
Nature Communications, Vol 15, Iss 1, Pp 1-10 (2024)
Subject
Language
English
ISSN
2041-1723
Abstract
Abstract The main protease (Mpro) of SARS-CoV-2 is critical for viral function and a key drug target. Mpro is only active when reduced; turnover ceases upon oxidation but is restored by re-reduction. This suggests the system has evolved to survive periods in an oxidative environment, but the mechanism of this protection has not been confirmed. Here, we report a crystal structure of oxidized Mpro showing a disulfide bond between the active site cysteine, C145, and a distal cysteine, C117. Previous work proposed this disulfide provides the mechanism of protection from irreversible oxidation. Mpro forms an obligate homodimer, and the C117-C145 structure shows disruption of interactions bridging the dimer interface, implying a correlation between oxidation and dimerization. We confirm dimer stability is weakened in solution upon oxidation. Finally, we observe the protein’s crystallization behavior is linked to its redox state. Oxidized Mpro spontaneously forms a distinct, more loosely packed lattice. Seeding with crystals of this lattice yields a structure with an oxidation pattern incorporating one cysteine-lysine-cysteine (SONOS) and two lysine-cysteine (NOS) bridges. These structures further our understanding of the oxidative regulation of Mpro and the crystallization conditions necessary to study this structurally.