Crystal Structure of African Swine Fever Virus pS273R Protease and Implications for Inhibitor Design
Guobang Li, Xiaoxia Liu, Mengyuan Yang, Guangshun Zhang, Zhengyang Wang, Kun Guo, Yuxue Gao, Peng Jiao, Jixue Sun, Cheng Chen, Hao Wang, Weilong Deng, Huihe Xiao, Sizheng Li, Haoru Wu, Ying Wang, Lin Cao, Zihan Jia, Luqing Shang, Cheng Yang, Yu Guo, Zihe Rao
Abstract
African swine fever virus, a large and complex icosahedral DNA virus, causes a deadly infection in domestic pigs. In addition to Africa and Europe, countries in Asia, including China, Vietnam, and Mongolia, were negatively affected by the hazards posed by ASFV outbreaks in 2018 and 2019, at which time more than 30 million pigs were culled. Until now, there has been no vaccine for protection against ASFV infection or effective treatments to cure ASF. Here, we solved the high-resolution crystal structure of the ASFV pS273R protease. The pS273R protease has a two-domain structure that distinguishes it from other members of the SUMO protease family, while the unique "arm domain" has been proven to be essential for its hydrolytic activity. Moreover, the peptidomimetic aldehyde compounds designed to target the substrate binding pocket exert prominent inhibitory effects and can thus be used in a potential lead for anti-ASFV drug development.