SARS-CoV-2 水溶性核壳蛋白的表达及其免疫原性分析。

Y B Wang, S W Wang, Q Y Jin, L P Chen, F Q Zhang, J J Shi, Y Yin, Z X Fan, X Y Liu, L P Wang, P Li
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摘要

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的冠状病毒病 2019(COVID-19)仍然是一个重大的公共卫生问题。核头壳(N)蛋白是 SARS-CoV-2 病毒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 蛋白对于开发检测 SARS-CoV-2 抗体的免疫测定方法和控制病毒传播至关重要。Western印迹和ELISA表明,重组N蛋白可被接种华卫SARS-CoV-2灭活疫苗的受试者血清识别。利用杂交瘤技术产生了四种单克隆抗体,即 2B1B1、4D3A3、5G1F8 和 7C6F5。在酶联免疫吸附试验中,这四种单克隆抗体的滴度都超过了 1.28×10.6.0。此外,在 IPMA 和 IFA 中,所有单克隆抗体都能与转染 pcDNA3.1-N 到 BHK-21 细胞中表达的 N 蛋白发生特异性反应。这些结果表明,水溶性 N 蛋白具有很高的免疫原性,并且与病毒上的原生 N 蛋白具有相同的表位。此外,水溶性 N 蛋白及其单克隆抗体的制备为 COVID-19 检测免疫分析的开发奠定了基础。
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Expression of water-soluble nucleocapsid protein of SARS-CoV-2 and analysis of its immunogenicity.

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.

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