| |  Online-Ressource |
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| Verfasst von: | Steuten, Kas [VerfasserIn]  |
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| | Kim, Heeyoung [VerfasserIn] |
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| | Widen, John C. [VerfasserIn] |
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| | Babin, Brett M. [VerfasserIn] |
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| | Onguka, Ouma [VerfasserIn] |
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| | Lovell, Scott [VerfasserIn] |
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| | Bolgi, Oguz [VerfasserIn] |
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| | Cerikan, Berati [VerfasserIn] |
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| | Neufeldt, Christopher [VerfasserIn] |
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| | Cortese, Mirko [VerfasserIn] |
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| | Muir, Ryan K. [VerfasserIn] |
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| | Bennett, John M. [VerfasserIn] |
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| | Geiss-Friedlander, Ruth [VerfasserIn] |
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| | Peters, Christoph [VerfasserIn] |
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| | Bartenschlager, Ralf [VerfasserIn] |
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| | Bogyo, Matthew [VerfasserIn] |
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| Titel: | Challenges for targeting SARS-CoV-2 proteases as a therapeutic strategy for COVID-19 |
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| Verf.angabe: | Kas Steuten, Heeyoung Kim, John C. Widen, Brett M. Babin, Ouma Onguka, Scott Lovell, Oguz Bolgi, Berati Cerikan, Christopher J. Neufeldt, Mirko Cortese, Ryan K. Muir, John M. Bennett, Ruth Geiss-Friedlander, Christoph Peters, Ralf Bartenschlager, and Matthew Bogyo |
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| E-Jahr: | 2021 |
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| Jahr: | February 11, 2021 |
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| Umfang: | 12 S. |
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| Teil: | volume:7 |
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| | year:2021 |
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| | number:6 |
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| | pages:1457-1468 |
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| | extent:12 |
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| Fussnoten: | Gesehen am 13.08.2021 |
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| Titel Quelle: | Enthalten in: American Chemical SocietyACS infectious diseases |
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| Ort Quelle: | Washington, DC : ACS Publ., 2015 |
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| Jahr Quelle: | 2021 |
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| Band/Heft Quelle: | 7(2021), 6, Seite 1457-1468 |
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| ISSN Quelle: | 2373-8227 |
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| Abstract: | Two proteases produced by the SARS-CoV-2 virus, the main protease and papain-like protease, are essential for viral replication and have become the focus of drug development programs for treatment of COVID-19. We screened a highly focused library of compounds containing covalent warheads designed to target cysteine proteases to identify new lead scaffolds for both Mpro and PLpro proteases. These efforts identified a small number of hits for the Mpro protease and no viable hits for the PLpro protease. Of the Mpro hits identified as inhibitors of the purified recombinant protease, only two compounds inhibited viral infectivity in cellular infection assays. However, we observed a substantial drop in antiviral potency upon expression of TMPRSS2, a transmembrane serine protease that acts in an alternative viral entry pathway to the lysosomal cathepsins. This loss of potency is explained by the fact that our lead Mpro inhibitors are also potent inhibitors of host cell cysteine cathepsins. To determine if this is a general property of Mpro inhibitors, we evaluated several recently reported compounds and found that they are also effective inhibitors of purified human cathepsins L and B and showed similar loss in activity in cells expressing TMPRSS2. Our results highlight the challenges of targeting Mpro and PLpro proteases and demonstrate the need to carefully assess selectivity of SARS-CoV-2 protease inhibitors to prevent clinical advancement of compounds that function through inhibition of a redundant viral entry pathway. |
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| DOI: | doi:10.1021/acsinfecdis.0c00815 |
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| URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext: https://doi.org/10.1021/acsinfecdis.0c00815 |
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| | DOI: https://doi.org/10.1021/acsinfecdis.0c00815 |
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| Datenträger: | Online-Ressource |
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| Sprache: | eng |
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| K10plus-PPN: | 1766788823 |
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| Verknüpfungen: | → Zeitschrift |
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Challenges for targeting SARS-CoV-2 proteases as a therapeutic strategy for COVID-19 / Steuten, Kas [VerfasserIn]; February 11, 2021 (Online-Ressource)
