应用噬菌体展示技术筛选、鉴定抗汉滩病毒单克隆抗体的模拟表位

Screening and identification of mimic epitopes of monoclonal antibodies against hantaan virus using phage display technique

目的 :应用噬菌体 12肽文库筛选抗汉滩病毒单抗 (mAb)F3、B11的模拟配体肽 ,并对其免疫学特性进行初步分析。方法 :以纯化的mAb为筛选配基 ,进行噬菌体肽库的生物亲和淘选。用ELISA法鉴定筛选克隆的结合活性 ,对阳性克隆进行序列测定和分析。用动物免疫试验初步分析噬菌体颗粒展示的抗原肽的免疫特性。结果 :通过 3～ 4轮生物淘选 ,ELISA显示筛选到的多数噬菌体克隆均可与mAb特异性结合 ;与mAbF3结合的阳性克隆的氨基酸序列高度一致 ,均为 MHGP TKNQMWHT ,与HTNV/SEOVM蛋白G2区第 75 0～ 75 9位氨基酸具有较高的同源性 ;而mAbB11特异性的结合肽在氨基酸水平上表现出一定的多态性 ,其序列的基序尚未能确定 ;动物免疫试验表明 ,噬菌体肽抗原具有良好的免疫反应性和免疫原性 ,是天然病毒抗原较好的免疫原模拟物。结论 :获得了具有良好结合活性的模拟表位肽 ,为基于表位的HFRSV多肽疫苗及DNA疫苗的研制奠定了基础。

AIM: To obtain mimic epitopes of monoclonal antibody (mAb) against Hantaan virus, and identify preliminarily their immunological characteristics. METHODS: Group-specific mAbs F3 and B11 were used as selective molecules for biopanning. After biopanning, the positive phages were identified by ELISA and DNA sequencing. Among the positive phages, F3-8, B11-18, B11-20 and B11-24 were selected to immunize BALB/c mice three times, respectively. The antiserum was then tittered and confirmed by sandwich ELISA and competition ELISA. RESULTS: After 3 to 4 rounds of effective screening, the majority of the selected clones were found able to react to mAb F3 or B11 in a dose-dependent manner, but not to BSA, rHBsAg or other unrelated mAbs. The amino acid sequences of the clones binding to mAb F3 contained an identical sequence MHGPTKNQMWHT, which had higher homology to 750-759 amino acids between a pair of cysteines within glycoprotein G2 of HTNV/SEOV, while those of clones binding to mAb B11 had no evident homologous regions within HTNV/SEOV proteins. The specific antibodies increased significantly following immunization with phage peptides, which indicated that the phage-displayed peptides had not only good antigenicity, but also strong immunoreactivity. CONCLUSION: The phage-displayed peptides could mimic the epitope of HFRSV antigen, which would provide the potential for preparing more effective epitope-based vaccines and specific diagnostic reagents.