In vitro enzyme characterization and several inhibitors for monkeypox virus core protease I7L

猴痘 病毒学 蛋白酶 体外 病毒 生物 生物化学 牛痘 重组DNA 基因
作者
Wei Lin,Yuqi Wu,Shuai Li,Jun Weng,M J Geng,Meng Mei,Z.-B. Wei
出处
期刊:Fems Microbiology Letters [Oxford University Press]
标识
DOI:10.1093/femsle/fnaf008
摘要

Monkeypox is a zoonotic viral disease caused by the monkeypox virus, a member of the genus Orthopoxvirus within the family Poxviridae, which also includes the variola virus. On Aug. 14, 2024, WHO Director-General declared monkeypox outbreak a public health emergency of international concern. Similar to variola virus core protease K7L, the I7L could be identified as a promising target to against monkeypox virus. Our work provides a solid foundation as well as specific molecular tools (protease production methods, assay design, inhibitor design) that can now be used to probe the function of I7L in vitro. Notably, in this work, various reported covalent lead compounds for COVID-19 proteases were screened and A68, shikonin and myricetin were identified as exhibiting high inhibitory activity against I7L. This work not only sheds light on effective inhibitors for the monkeypox virus core protease but also contributes to the broader search for antiviral agents targeting this enzyme.

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