1. A cysteine protease inhibitor blocks SARS-CoV-2 infection of human and monkey cells
- Author
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Ken Hirata, Sungjun Beck, Hong Wang, Tat, Pavla Fajtová, Balachandra Chenna, Daniel C Maneval, Brett L. Hurst, Hsu J, Thomas D. Meek, Ardala Katzfuss, Anthony J. O’Donoghue, Frank M. Raushel, Li Li, Chien-Te K Tseng, Klaudia I. Kocurek, Kostomiris Dh, Aaron F. Carlin, Danielle E. Skinner, Felix W Frueh, Miriam A. Giardini, Jiyun Zhu, Zane W. Taylor, Aleksandra Drelich, Drake M. Mellott, de Siqueira-Neto Jl, Laura Beretta, James H. McKerrow, and Alex E. Clark
- Subjects
Proteases ,K777 ,Cathepsin L ,Phenylalanine ,viruses ,Microbial Sensitivity Tests ,Cysteine Proteinase Inhibitors ,spike protein ,Biochemistry ,Antiviral Agents ,Cathepsin B ,Piperazines ,Article ,protease inhibitor ,Tosyl Compounds ,Protein Domains ,Cell Line, Tumor ,Chlorocebus aethiops ,Animals ,Humans ,Vero Cells ,Cathepsin ,Infectivity ,biology ,Chemistry ,SARS-CoV-2 ,Articles ,Biological Sciences ,Virus Internalization ,Cysteine protease ,Molecular biology ,Proteolysis ,Spike Glycoprotein, Coronavirus ,Vero cell ,biology.protein ,Cysteine - Abstract
K777 is a di-peptide analog that contains an electrophilic vinyl-sulfone moiety and is a potent, covalent inactivator of cathepsins. Vero E6, HeLa/ACE2, Caco-2, A549/ACE2, and Calu-3, cells were exposed to SARS-CoV-2, and then treated with K777. K777 reduced viral infectivity with EC50 values of inhibition of viral infection of: 74 nM for Vero E6, 50 values in the low micromolar range. No toxicity of K777 was observed for any of the host cells at 10-100 μM inhibitor. K777 did not inhibit activity of the papain-like cysteine protease and 3CL cysteine protease, encoded by SARS-CoV-2 at concentrations of ≤ 100 μM. These results suggested that K777 exerts its potent anti-viral activity by inactivation of mammalian cysteine proteases which are essential to viral infectivity. Using a propargyl derivative of K777 as an activity-based probe, K777 selectively targeted cathepsin B and cathepsin L in Vero E6 cells. However only cathepsin L cleaved the SARS-CoV-2 spike protein and K777 blocked this proteolysis. The site of spike protein cleavage by cathepsin L was in the S1 domain of SARS-CoV-2, differing from the cleavage site observed in the SARS CoV-1 spike protein. These data support the hypothesis that the antiviral activity of K777 is mediated through inhibition of the activity of host cathepsin L and subsequent loss of viral spike protein processing.SIGNIFICANCEThe virus causing COVID-19 is highly infectious and has resulted in a global pandemic. We confirm that a cysteine protease inhibitor, approved by the FDA as a clinical-stage compound, inhibits SARS-CoV-2 infection of several human and monkey cell lines with notable(nanomolar) efficacy. The mechanism of action of this inhibitor is identified as a specific inhibition of host cell cathepsin L. This in turn inhibits host cell processing of the coronaviral spike protein, a step required for cell entry. Neither of the coronaviral proteases are inhibited, and the cleavage site of spike protein processing is different from that reported in other coronaviruses. Hypotheses to explain the differential activity of the inhibitor with different cell types are discussed.
- Published
- 2020