Dimethyl sulfoxide reduces the stability but enhances catalytic activity of the main SARS-CoV-2 protease 3CLpro

dc.authorid0000-0003-3579-4552
dc.authorid0000-0001-5950-3436
dc.contributor.authorFerreira, Juliana C.
dc.contributor.authorFadl, Samar
dc.contributor.authorİlter, Metehan
dc.contributor.authorPekel, Hanife
dc.contributor.authorRezgui, Rachid
dc.contributor.authorŞensoy, Özge
dc.contributor.authorRabeh, Wael M.
dc.date.accessioned2021-08-13T06:42:22Z
dc.date.available2021-08-13T06:42:22Z
dc.date.issued2021
dc.departmentİstanbul Medipol Üniversitesi, Mühendislik ve Doğa Bilimleri Fakültesi, Bilgisayar Mühendisliği Bölümü
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Rejeneratif ve Restoratif Tıp Araştırmaları Merkezi (REMER)
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Sağlık Bilim ve Teknolojileri Araştırma Enstitüsü
dc.departmentİstanbul Medipol Üniversitesi, Sağlık Hizmetleri Meslek Yüksekokulu, Eczane Hizmetleri Ana Bilim Dalı
dc.description.abstractSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for coronavirus disease 2019 (COVID-19), one of the most challenging global pandemics of the modern era. Potential treatment strategies against COVID-19 are yet to be devised. It is crucial that antivirals that interfere with the SARS-CoV-2 life cycle be identified and developed. 3-Chymotrypsin-like protease (3CLpro) is an attractive antiviral drug target against SARS-CoV-2, and coronaviruses in general, because of its role in the processing of viral polyproteins. Inhibitors of 3CLpro activity are screened in enzyme assays before further development of the most promising leads. Dimethyl sulfoxide (DMSO) is a common additive used in such assays and enhances the solubility of assay components. However, it may also potentially affect the stability and efficiency of 3CLpro but, to date, this effect had not been analyzed in detail. Here, we investigated the effect of DMSO on 3CLpro-catalyzed reaction. While DMSO (5%-20%) decreased the optimum temperature of catalysis and thermodynamic stability of 3CLpro, it only marginally affected the kinetic stability of the enzyme. Increasing the DMSO concentration up to 20% improved the catalytic efficiency and peptide-binding affinity of 3CLpro. At such high DMSO concentration, the solubility and stability of peptide substrate were improved because of reduced aggregation. In conclusion, we recommend 20% DMSO as the minimum concentration to be used in screens of 3CLpro inhibitors as lead compounds for the development of antiviral drugs against COVID-19.
dc.identifier.citationFerreira, J. C., Fadl, S., İlter, M., Pekel, H., Rezgui, R., Şensoy, Ö. ... Rabeh, W. M. (2021). Dimethyl sulfoxide reduces the stability but enhances catalytic activity of the main SARS-CoV-2 protease 3CLpro. FASEB Journal, 35(8). https://dx.doi.org/10.1096/fj.202100994
dc.identifier.doi10.1096/fj.202100994
dc.identifier.issn0892-6638
dc.identifier.issn1530-6860
dc.identifier.issue8
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://dx.doi.org/10.1096/fj.202100994
dc.identifier.urihttps://hdl.handle.net/20.500.12511/7808
dc.identifier.volume35
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofFASEB Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsAttribution-NonCommercial 4.0 International*
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/*
dc.subject3-Chymotrypsin-Like Protease (3CLpro)
dc.subjectCOVID-19
dc.subjectDMSO
dc.subjectInitial Velocity
dc.subjectSARS-Cov-2
dc.subjectThermodynamic Stability
dc.titleDimethyl sulfoxide reduces the stability but enhances catalytic activity of the main SARS-CoV-2 protease 3CLpro
dc.typeArticle

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