Interfering with Host Proteases in SARS-CoV-2 Entry as a Promising Therapeutic Strategy

التفاصيل البيبلوغرافية
العنوان: Interfering with Host Proteases in SARS-CoV-2 Entry as a Promising Therapeutic Strategy
المؤلفون: Philip Maximilian Knaff, Patrick Müller, Tanja Schirmeister, Stefan Hammerschmidt, Hannah Maus, Christian Kersten, Volker Mailänder
المصدر: Current Medicinal Chemistry. 29:635-665
بيانات النشر: Bentham Science Publishers Ltd., 2022.
سنة النشر: 2022
مصطلحات موضوعية: Pharmacology, Serine protease, Cathepsin, Proteases, biology, SARS-CoV-2, Organic Chemistry, Virus Internalization, medicine.disease_cause, Biochemistry, Virology, Transmembrane protein, Virus, COVID-19 Drug Treatment, Spike Glycoprotein, Coronavirus, Drug Discovery, biology.protein, medicine, Humans, Molecular Medicine, Serine Proteases, Receptor, Furin, Coronavirus
الوصف: Abstract: Due to its fast international spread and substantial mortality, the coronavirus disease COVID-19 evolved to a global threat. Since there is currently no causative drug against this viral infection available, science is striving for new drugs and other approaches to treat the new disease. Studies have shown that the cell entry of coronaviruses into host cells takes place through the binding of the viral spike (S) protein to cell receptors. Priming of the S protein occurs via hydrolysis by different host proteases. The inhibition of these proteases could impair the processing of the S protein, thereby affecting the interaction with the host-cell receptors and preventing virus cell entry. Hence, inhibition of these proteases could be a promising strategy for treatment against SARSCoV- 2. In this review, we discuss the current state of the art of developing inhibitors against the entry proteases furin, the transmembrane serine protease type-II (TMPRSS2), trypsin, and cathepsin L.
تدمد: 0929-8673
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c69c51f6e64a7ee53cc1fbf4047b321
https://doi.org/10.2174/0929867328666210526111318
رقم الأكسشن: edsair.doi.dedup.....9c69c51f6e64a7ee53cc1fbf4047b321
قاعدة البيانات: OpenAIRE