Petushkova Anastasiia I, Zamyatnin Andrey A
Institute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.
Pharmaceuticals (Basel). 2020 Sep 28;13(10):277. doi: 10.3390/ph13100277.
Papain-like proteases (PLpro) of coronaviruses (CoVs) support viral reproduction and suppress the immune response of the host, which makes CoV PLpro perspective pharmaceutical targets. Their inhibition could both prevent viral replication and boost the immune system of the host, leading to the speedy recovery of the patient. Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the third CoV outbreak in the last 20 years. Frequent mutations of the viral genome likely lead to the emergence of more CoVs. Inhibitors for CoV PLpro can be broad-spectrum and can diminish present and prevent future CoV outbreaks as PLpro from different CoVs have conservative structures. Several inhibitors have been developed to withstand SARS-CoV and Middle East respiratory syndrome CoV (MERS-CoV). This review summarizes the structural features of CoV PLpro, the inhibitors that have been identified over the last 20 years, and the compounds that have the potential to become novel effective therapeutics against CoVs in the near future.
冠状病毒(CoV)的木瓜蛋白酶样蛋白酶(PLpro)有助于病毒繁殖并抑制宿主的免疫反应,这使得CoV PLpro成为有前景的药物靶点。对它们的抑制作用既能阻止病毒复制,又能增强宿主的免疫系统,从而使患者迅速康复。由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019冠状病毒病(COVID-19)是过去20年中的第三次冠状病毒爆发。病毒基因组的频繁突变可能导致更多冠状病毒的出现。由于不同冠状病毒的PLpro具有保守结构,因此针对CoV PLpro的抑制剂可能具有广谱性,可减少当前的冠状病毒爆发并预防未来可能出现的爆发。已经开发出几种抑制剂来对抗严重急性呼吸综合征冠状病毒(SARS-CoV)和中东呼吸综合征冠状病毒(MERS-CoV)。本文综述了CoV PLpro的结构特征、过去20年中已鉴定出的抑制剂,以及在不久的将来有可能成为对抗冠状病毒的新型有效疗法的化合物。