摘要
目的筛选SARS病毒S蛋白的B细胞表位。方法使用SARS-CoV S DNA疫苗免疫BALB/c小鼠,获得SARS病毒S蛋白的免疫血清。人工合成包含169条部分氨基酸序列重叠的SARS-CoV S蛋白的多肽库。将多肽片段包被ELISA板,利用免疫小鼠血清,通过抗体结合试验来筛选SARS病毒S蛋白的线性B细胞表位。并将筛选结果与使用B细胞表位分析软件预测的结果进行比较。结果使用重叠肽合成法筛选到SARS-CoV蛋白两条多肽片段S335-352和S442-458,能与免疫动物血清特异性结合,与使用Bcipep数据库预测B细胞表位的结果相一致。结论鉴定了两个新的SARS病毒S蛋白B细胞表位。
Objective Identification of antibody epitopes in the severe acute respiratory syndrome eoronavirus spike glycoprotein. Method BALB/c mice were immunized with SARS-CoV S DNA vaccine, and sera were collected from immunized mice. 169 peptides contained overlapped peptide pool which covered the whole SARS-CoV S protein were synthesized. ELISA plate was coated with the peptides and B cell epitopes were determined by antibody binding test by sera from DNA vaccine immunized mice. The results were compared with that predicted by Bcipep data. Result Sera from SARS-CoV S DNA vaccine immunized mice reacted with the peptides of S335-352 and S442-458 among 169 SARS- CoV S peptides. These two antibody epitopes also can be predicted by Bcipep data. Conclusion Two new B cell epitopes of SARS-CoV spike protein were identified in mice following SARS-CoV S DNA vaccination.
出处
《热带医学杂志》
CAS
2009年第2期161-163,184,共4页
Journal of Tropical Medicine
基金
国家科技部863项目(No.2007AA02Z415)
广州市2008年第5批科学技术经费项目(No.2008J1-C141-3)