Title Screening of small-molecule libraries using SARS-CoV-2-derived sequences identifies novel Furin inhibitors /
Authors Jorkesh, Alireza ; Rothenberger, Sylvia ; Baldassar, Laura ; Grybaite, Birute ; Kavaliauskas, Povilas ; Mickevicius, Vytautas ; Dettin, Monica ; Vascon, Filippo ; Cendron, Laura ; Pasquato, Antonella
DOI 10.3390/ijms25105079
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Is Part of International journal of molecular sciences.. MDPI. 2024, vol. 25, iss. 10, art. no. 5079, p. 1-21.. ISSN 1422-0067. eISSN 1422-0067
Keywords [eng] Furin ; protease ; SARS-CoV-2 ; cleavage ; inhibitor ; in vitro ; HTS ; envelope glycoprotein ; virus ; exosite ; peptide
Abstract [eng] SARS-CoV-2 is the pathogen responsible for the most recent global pandemic, which has claimed hundreds of thousands of victims worldwide. Despite remarkable efforts to develop an effective vaccine, concerns have been raised about the actual protection against novel variants. Thus, researchers are eager to identify alternative strategies to fight against this pathogen. Like other opportunistic entities, a key step in the SARS-CoV-2 lifecycle is the maturation of the envelope glycoprotein at the RARR685↓ motif by the cellular enzyme Furin. Inhibition of this cleavage greatly affects viral propagation, thus representing an ideal drug target to contain infection. Importantly, no Furin-escape variants have ever been detected, suggesting that the pathogen cannot replace this protease by any means. Here, we designed a novel fluorogenic SARS-CoV-2-derived substrate to screen commercially available and custom-made libraries of small molecules for the identification of new Furin inhibitors. We found that a peptide substrate mimicking the cleavage site of the envelope glycoprotein of the Omicron variant (QTQTKSHRRAR-AMC) is a superior tool for screening Furin activity when compared to the commercially available Pyr-RTKR-AMC substrate. Using this setting, we identified promising novel compounds able to modulate Furin activity in vitro and suitable for interfering with SARS-CoV-2 maturation. In particular, we showed that 3-((5-((5-bromothiophen-2-yl)methylene)-4-oxo-4,5 dihydrothiazol-2-yl)(3-chloro-4-methylphenyl)amino)propanoic acid (P3, IC50 = 35 μM) may represent an attractive chemical scaffold for the development of more effective antiviral drugs via a mechanism of action that possibly implies the targeting of Furin secondary sites (exosites) rather than its canonical catalytic pocket. Overall, a SARS-CoV-2-derived peptide was investigated as a new substrate for in vitro high-throughput screening (HTS) of Furin inhibitors and allowed the identification of compound P3 as a promising hit with an innovative chemical scaffold. Given the key role of Furin in infection and the lack of any Food and Drug Administration (FDA)-approved Furin inhibitor, P3 represents an interesting antiviral candidate.
Published MDPI
Type Journal article
Language English
Publication date 2024
CC license CC license description