Institute of Molecular Genetics of National Research Centre Kurchatov Institute, Moscow, Russian Federation.
PLoS One. 2022 May 24;17(5):e0266015. doi: 10.1371/journal.pone.0266015. eCollection 2022.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of coronavirus disease 2019 (COVID-19) which has extremely rapidly spread worldwide. In order to develop the effective antiviral therapies, it is required to understand the molecular mechanisms of the SARS-CoV-2 pathogenesis. The main protease, or 3C-like protease (3CLpro), plays the essential role in the coronavirus replication that makes the enzyme a promising therapeutic target. Viral enzymes are known to be multifunctional. Particularly, 3CLpro of SARS-CoV was shown to induce apoptosis in addition to its main function. In the present study we analyzed the cytotoxicity of active SARS-CoV-2 3CLpro and its inactivated form upon their individual expression in four human cell lines. For this purpose, we constructed a protein biosensor which allows to detect the proteolytic activity of SARS-CoV-2 3CLpro and confirmed the expression of the active protease in all cell lines used. We studied viability and morphology of the cells and found that both active and inactivated enzyme variants induce no cell death in contrast to the homologous 3CL protease of SARS-CoV. These results indicate that SARS-CoV-2 3CLpro is unlikely contribute to the cytopathic effect observed during viral infection directly.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是 2019 年冠状病毒病(COVID-19)的病原体,它在全球范围内迅速传播。为了开发有效的抗病毒疗法,需要了解 SARS-CoV-2 发病机制的分子机制。主要蛋白酶,或 3C 样蛋白酶(3CLpro),在冠状病毒复制中起着至关重要的作用,使该酶成为有前途的治疗靶点。众所周知,病毒酶具有多功能性。特别是,SARS-CoV 的 3CLpro 除了其主要功能外,还被证明能诱导细胞凋亡。在本研究中,我们分析了在四种人类细胞系中单独表达的活性 SARS-CoV-2 3CLpro 及其失活形式的细胞毒性。为此,我们构建了一种蛋白质生物传感器,该传感器可检测 SARS-CoV-2 3CLpro 的蛋白水解活性,并证实了在所有使用的细胞系中均表达了活性蛋白酶。我们研究了细胞的活力和形态,发现与 SARS-CoV 的同源 3CL 蛋白酶相比,活性和失活的酶变体均不会诱导细胞死亡。这些结果表明,SARS-CoV-2 3CLpro 不太可能直接导致病毒感染过程中观察到的细胞病变效应。