School of Public Health, Xinxiang Medical University, Xinxiang 453003, P.R. China.
School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang 453003, P.R. China.
Pol J Vet Sci. 2023 Dec 12;26(4):571-579. doi: 10.24425/pjvs.2023.148277.
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to be a major public health concern. Nucleocapsid (N) protein is the most abundant structural protein on SARS-CoV-2 virions and induces the production of antibodies at the early stage of infection. Large-scale preparation of N protein is essential for the development of immunoassays to detect antibodies to SARS-CoV-2 and the control of virus transmission. In this study, expression of water-soluble N protein was achieved through inducing protein expression at 25°C with 0.5 mM IPTG for 12 h. Western blot and ELISA showed that recombinant N protein could be recognized by sera collected from subjects immunized with Sinovac inactivated SARS-CoV-2 vaccine. Four monoclonal antibodies namely 2B1B1, 4D3A3, 5G1F8, and 7C6F5 were produced using hybridoma technology. Titers of all four monoclonal antibodies in ELISA reached more than 1.28×10 6.0. Moreover, all monoclonal antibodies could react specifically with N protein expressed by transfection of pcDNA3.1-N into BHK-21 cells in IPMA and IFA. These results indicated that water-soluble N protein retained high immunogenicity and possessed the same epitopes as that of native N protein on virions. In addition, the preparation of water-soluble N protein and its monoclonal antibodies laid the basis for the development of immunoassays for COVID-19 detection.
新型冠状病毒病(COVID-19)由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起,仍是一项重大公共卫生关注点。核衣壳(N)蛋白是 SARS-CoV-2 病毒粒子上最丰富的结构蛋白,可在感染早期诱导产生抗体。大规模制备 N 蛋白对于开发用于检测 SARS-CoV-2 抗体的免疫测定以及控制病毒传播至关重要。在本研究中,通过在 25°C 下用 0.5mM IPTG 诱导蛋白表达 12 小时来实现水溶性 N 蛋白的表达。Western blot 和 ELISA 显示,用科兴公司生产的 SARS-CoV-2 灭活疫苗免疫的受试者血清可识别重组 N 蛋白。使用杂交瘤技术生产了四种单克隆抗体,分别为 2B1B1、4D3A3、5G1F8 和 7C6F5。在 ELISA 中,这四种单克隆抗体的滴度均超过 1.28×10 6.0。此外,所有单克隆抗体均能在 IPMA 和 IFA 中特异性识别 pcDNA3.1-N 转染 BHK-21 细胞表达的 N 蛋白。这些结果表明,水溶性 N 蛋白保留了高免疫原性,并且与病毒粒子上天然 N 蛋白具有相同的表位。此外,水溶性 N 蛋白的制备及其单克隆抗体的制备为 COVID-19 检测免疫测定的开发奠定了基础。