Department of Histology and Embryology, School of Basic Medicine, Third Military Medical University, Chongqing 400038, People's Republic of China.
Appl Microbiol Biotechnol. 2013 Feb;97(4):1553-60. doi: 10.1007/s00253-012-4419-z. Epub 2012 Oct 19.
Dengue virus is a major international public health concern, and there is a lack of available effective vaccines. Virus-specific epitopes could help in developing epitope peptide vaccine. Previously, a neutralizing monoclonal antibody (mAb) 4F5 against nonstructural protein 3 (NS3) of dengue virus 2 (DV2) was developed in our lab. In this work, the B cell epitope recognized by mAb 4F5 was identified using the phage-displayed peptide library. The results of the binding assay and competitive inhibition assay indicated that the peptides, residues 460-469 (U460-469 RVGRNPKNEN) of DV2 NS3 protein, were the B cell epitopes recognized by mAb 4F5. Furthermore, the epitope peptides and a control peptide were synthesized and then immunized female BALB/c mice. ELISA analysis showed that immunization with synthesized epitope peptide elicited a high level of antibody in mice, and immunofluorescent staining showed that the antisera from fusion epitope-immunized mice also responded to DV2 NS3 protein, which further characterized the specific response of the present epitope peptide. Therefore, the present work revealed the specificity of the newly identified epitope (U460-469) of DV2 NS3 protein, which may shed light on dengue virus (DV) vaccine design, DV pathogenesis study, and even DV diagnostic reagent development.
登革热病毒是一个主要的国际公共卫生关注点,目前缺乏有效的可用疫苗。病毒特异性表位有助于开发表位肽疫苗。此前,我们实验室研发了一种针对登革热病毒 2 型(DV2)非结构蛋白 3(NS3)的中和单克隆抗体(mAb)4F5。在这项工作中,使用噬菌体展示肽文库鉴定了 mAb 4F5 识别的 B 细胞表位。结合实验和竞争抑制实验的结果表明,DV2 NS3 蛋白的残基 460-469(U460-469 RVGRNPKNEN)为 mAb 4F5 识别的 B 细胞表位。此外,合成了表位肽和对照肽,并对雌性 BALB/c 小鼠进行了免疫。ELISA 分析表明,合成表位肽免疫可使小鼠产生高水平的抗体,免疫荧光染色显示融合表位免疫小鼠的抗血清也可与 DV2 NS3 蛋白反应,进一步证实了本研究表位肽的特异性反应。因此,本研究揭示了 DV2 NS3 蛋白新鉴定的表位(U460-469)的特异性,这可能为登革热病毒(DV)疫苗设计、DV 发病机制研究甚至 DV 诊断试剂的开发提供线索。