School of Life Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
School of Life Sciences, Zhengzhou University, Zhengzhou 450001, Henan, China.
Int J Biol Macromol. 2021 Sep 30;187:683-689. doi: 10.1016/j.ijbiomac.2021.07.168. Epub 2021 Jul 30.
Glycoprotein 3 (GP3), a highly glycosylated membrane protein, is a protective antigen and minor structural protein of porcine reproductive and respiratory syndrome virus (PRRSV), and plays a crucial role in virus assembly and infection. In the present study, we synthesized 23 overlapping peptides span GP3 protein sequence and used pig anti-PRRSV serums to identify immunodominant peptides by indirect ELISA. Five immunodominant peptides GP3-P3, P4, P5, P6 and P7 were identified and GP3-P4 (PLCPTRQAAAEILEPGKS) was conjugated to carrier protein BSA. One mAb 1E5 against GP3 was generated from BALB/c mice immunized with the conjugates BSA-P4. The Characterization of mAb was identified by Western blot, Dot-ELISA, IPMA and IFA. We found that mAb 1E5 can specifically react with HP-PRRSV strains but not C-PRRSV or NADC30-like PRRSV strains tested in this study. Site-directed alanine substitution analysis revealed that 8 amino acid residues were involved in antibody binding, among them E65, L67 and P69 were critical residue recognized by mAb 1E5. Taken together, this study provided a novel strategy for generating specific mAbs against virus proteins by using immunodominant peptides as targets, and the mAb 1E5 may be useful for development of rapid differential detection method differentiating HP-PRRSV from C-PRRSV and NADC30-like PRRSV.
糖蛋白 3(GP3)是一种高度糖基化的膜蛋白,是猪繁殖与呼吸综合征病毒(PRRSV)的保护性抗原和次要结构蛋白,在病毒组装和感染中起关键作用。本研究合成了 23 个重叠肽,跨越 GP3 蛋白序列,并使用猪抗 PRRSV 血清通过间接 ELISA 鉴定免疫显性肽。鉴定出 5 个免疫显性肽 GP3-P3、P4、P5、P6 和 P7,并将 GP3-P4(PLCPTRQAAAEILEPGKS)与载体蛋白 BSA 缀合。用 BSA-P4 免疫 BALB/c 小鼠产生了针对 GP3 的单克隆抗体 1E5。通过 Western blot、Dot-ELISA、IPMA 和 IFA 鉴定了 mAb 的特性。我们发现 mAb 1E5 可以特异性地与 HP-PRRSV 株反应,但不能与本研究中测试的 C-PRRSV 或 NADC30 样 PRRSV 株反应。定点丙氨酸取代分析显示,8 个氨基酸残基参与抗体结合,其中 E65、L67 和 P69 是 mAb 1E5 识别的关键残基。总之,这项研究提供了一种通过使用免疫显性肽作为靶点生成针对病毒蛋白的特异性 mAb 的新策略,mAb 1E5 可能有助于开发快速区分检测方法,区分 HP-PRRSV 与 C-PRRSV 和 NADC30 样 PRRSV。