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Structural Basis for Inhibiting Porcine Epidemic Diarrhea Virus Replication with the 3C-Like Protease Inhibitor GC376

mdpi. 2020-02; 
Gang Ye ,, Xiaowei Wang ,, Xiaohan Tong , Yuejun Shi , Zhen F. Fu ,, and Guiqing Peng ,,*
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Proteins, Expression, Isolation and Analysis The fluorescent peptide substrate “Dabcyl-YNSTLQ↓AGLRKM-E-Edans” (GenScript, Piscataway, NJ, USA), which contains the N-terminal cleavage site of the PEDV 3CLpro, was used in FRET assays. Get A Quote

摘要

Porcine epidemic diarrhea virus (PEDV), being highly virulent and contagious in piglets, has caused significant damage to the pork industries of many countries worldwide. There are no commercial drugs targeting coronaviruses (CoVs), and few studies on anti-PEDV inhibitors. The coronavirus 3C-like protease (3CLpro) has a conserved structure and catalytic mechanism and plays a key role during viral polyprotein processing, thus serving as an appealing antiviral drug target. Here, we report the anti-PEDV effect of the broad-spectrum inhibitor GC376 (targeting 3Cpro or 3CLpro?of viruses in the picornavirus-like supercluster). GC376 was highly effective against the PEDV 3CLpro?and exerted similar inhibitory effects... More

關鍵詞

coronavirus; PEDV 3CLpro; inhibitor; crystal structure; complex
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