摘要
Porcine epidemic diarrhea virus (PEDV) causes high mortality in pigs. PEDV main protease (M-pro) plays an essential role in viral replication. We solved the structure of PEDV complexed with peptidomimetic inhibitor N3 carrying a Michael acceptor warhead, revealing atomic level interactions. We further designed a series of 17 inhibitors with altered side groups. Inhibitors M2 and M17 demonstrated enhanced specificity against PEDV M-pro. These compounds have potential as future therapeutics to combat PEDV infection.
- 出版日期2017-4-13
- 单位天津大学