1. Dimeric and monomeric conformation of SARS-CoV-2 main protease: New technical approaches based on IR radiation.
- Author
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Piccirilli F, Vondracek H, Silvestrini L, Parisse P, Spinozzi F, Vaccari L, Toma A, Aglieri V, Casalis L, Piccionello AP, Mariani P, Birarda G, and Ortore MG
- Subjects
- Protein Multimerization drug effects, Infrared Rays, Humans, COVID-19 virology, Betacoronavirus enzymology, Betacoronavirus drug effects, Viral Nonstructural Proteins antagonists & inhibitors, Viral Nonstructural Proteins metabolism, Viral Nonstructural Proteins chemistry, Cysteine Endopeptidases metabolism, Cysteine Endopeptidases chemistry, Protein Conformation, SARS-CoV-2 enzymology, SARS-CoV-2 drug effects, Coronavirus 3C Proteases metabolism, Coronavirus 3C Proteases antagonists & inhibitors, Coronavirus 3C Proteases chemistry, Spectrophotometry, Infrared
- Abstract
The main proteases M
pro are a group of highly conserved cysteine hydrolases in β-coronaviruses. They have been demonstrated to play an unavoidable role in viral replication, and consequently they have been suggested as key targets for treating coronavirus-caused infectious diseases, mainly from the COVID-19 epidemic. Since the most functional form for Mpro enzymatic activity is associated to its homodimer, compounds inhibiting dimerization should also inhibit catalytic activity. We show how PIR-SEIRA (Plasmonic Internal Reflection-Surface Enhanced InfraRed Absorption) spectroscopy can be a noteworthy technique to study proteins subtle structural variations associated to inhibitor binding. Nanoantennas arrays can selectively confine and enhance electromagnetic field via localized plasmonic resonances, thus promoting ultrasensitive detection of biomolecules in close proximity of nanoantenna arrays and enabling the effective investigation of protein monolayers. By adopting this approach, reflection measurements conducted under back illumination of nanoantennas allow to probe anchored protein monolayers, with minimum contribution of environmental buffer molecules. PIR-SEIRA spectroscopy on Mpro was carried out by ad hoc designed devices, resonating in the spectral region of Amide I and Amide II bands. We evaluated here the structure of anchored monomers and dimers in different buffered environment and in presence of a newly designed Mpro inhibitor. Experimental results show that dimerization is not associated to relevant backbone rearrangements of the protein at secondary structure level, and even if the compound inhibits the dimerization, it is not effective at breaking preformed dimers., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.)- Published
- 2024
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