Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing, China; School of Biological Science and Medical Engineering, Beihang University, Beijing China.
School of Biological Science and Medical Engineering, Beihang University, Beijing China.
Virus Res. 2020 Oct 15;288:198082. doi: 10.1016/j.virusres.2020.198082. Epub 2020 Jul 1.
The outbreak of the 2019 novel coronavirus (SARS-CoV-2) has infected millions of people with a large number of deaths across the globe. The existing therapies are limited in dealing with SARS-CoV-2 due to the sudden appearance of the virus. Therefore, vaccines and antiviral medicines are in desperate need. We took immune-informatics approaches to identify B- and T-cell epitopes for surface glycoprotein (S), membrane glycoprotein (M) and nucleocapsid protein (N) of SARS-CoV-2, followed by estimating their antigenicity and interactions with the human leukocyte antigen (HLA) alleles. Allergenicity, toxicity, physiochemical properties analysis and stability were examined to confirm the specificity and selectivity of the epitope candidates. We identified a total of five B cell epitopes in RBD of S protein, seven MHC class-I, and 18 MHC class-II binding T-cell epitopes from S, M and N protein which showed non-allergenic, non-toxic and highly antigenic features and non-mutated in 55,179 SARS-CoV-2 virus strains until June 25, 2020. The epitopes identified here can be a potentially good candidate repertoire for vaccine development.
2019 年新型冠状病毒(SARS-CoV-2)的爆发感染了数百万人,并在全球范围内造成了大量死亡。由于该病毒的突然出现,现有的治疗方法在应对 SARS-CoV-2 方面受到限制。因此,疫苗和抗病毒药物急需开发。我们采用免疫信息学方法来鉴定 SARS-CoV-2 表面糖蛋白(S)、膜糖蛋白(M)和核衣壳蛋白(N)的 B 细胞和 T 细胞表位,然后评估它们的抗原性以及与人类白细胞抗原(HLA)等位基因的相互作用。我们还对表位候选物的变应原性、毒性、理化性质和稳定性进行了分析,以确认其特异性和选择性。我们从 S、M 和 N 蛋白中总共鉴定出 S 蛋白的 RBD 中的五个 B 细胞表位、七个 MHC Ⅰ类和 18 个 MHC Ⅱ类结合 T 细胞表位,这些表位具有非变应原性、非毒性和高抗原性的特征,并且在截至 2020 年 6 月 25 日的 55179 株 SARS-CoV-2 病毒中未发生突变。这里鉴定的表位可以作为疫苗开发的潜在良好候选物。