Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Moscow State University, Moscow, Russia.
Dokl Biochem Biophys. 2023 Dec;513(Suppl 1):S63-S66. doi: 10.1134/S1607672923700709. Epub 2024 Feb 20.
Two eukaryotic cell lines, A549 and A431, with stable expression of the nucleocapsid protein (N-protein) of the SARS-CoV-2 virus fused with the red fluorescent protein mRuby3 were obtained. Using microscopy, the volumes of the cytoplasm and nucleus were determined for these cells. Using quantitative immunoblotting techniques, the concentrations of the N-mRuby3 fusion protein in their cytoplasm were assessed. They were 19 and 9 μM for A549 and A431 cells, respectively. Using these concentrations, the initial rate of N-protein degradation in the studied cells was estimated from the decrease in cell fluorescence. In A549 and A431 cells, it was the same (84 nM per hour). The approach of quantitatively describing the degradation process can be applied to analyze the effectiveness of a wide class of antiviral drugs that cause degradation of viral proteins.
获得了两种稳定表达 SARS-CoV-2 病毒核衣壳蛋白(N 蛋白)与红色荧光蛋白 mRuby3 融合产物的真核细胞系 A549 和 A431。使用显微镜测量了这些细胞的细胞质和细胞核体积。使用定量免疫印迹技术评估了其细胞质中 N-mRuby3 融合蛋白的浓度。A549 和 A431 细胞的浓度分别为 19 和 9 μM。根据细胞荧光强度的降低,使用这些浓度估计了研究细胞中 N 蛋白降解的初始速率。在 A549 和 A431 细胞中,其速率相同(每小时 84 nM)。这种定量描述降解过程的方法可用于分析广泛类别的抗病毒药物的效果,这些药物可导致病毒蛋白降解。