利用噬菌体展示技术筛选草鱼呼肠孤病毒VP39蛋白相互作用多肽

VP39是草鱼呼肠孤Ⅲ型病毒(GCRV GenotypeⅢ, GCRV-Ⅲ)S9基因编码的蛋白,为研究VP39蛋白在GCRV-Ⅲ感染草鱼细胞过程中行使的生物学功能,将克隆VP39基因序列并构建原核表达载体pET32a-VP39,通过原核表达得到VP39-HIS融合蛋白;利用VP39蛋白溶液免疫小鼠,制备鼠抗VP39多克隆抗体,通过Western Blot对抗体进行评估;利用制备的多克隆抗体探究GCRV-Ⅲ感染细胞过程中VP39蛋白表达动力学;利用噬菌体展示技术筛选与VP39蛋白特异性结合的多肽序列并进行分析。SDS-PAGE电泳结果显示, VP39-HIS融合蛋白可良好溶于PBS中,蛋白大小约为39 kD; Western Blot检测表明实验所制备的VP39多克隆抗体在1:10000稀释比例下,既能识别原核表达的VP39-HIS融合蛋白,也能识别GCRV-Ⅲ感染CIK细胞后表达的VP39蛋白,具有良好的效价与特异性;在病毒侵染过程中, VP39前期表达量较少,在中后期大量表达;噬菌体展示技术筛选出两条多肽与VP39蛋白有高度亲和性,经过在NCBI上比对后发现草鱼基因组中有7个基因与筛...

SCREENING OF PEPTIDES INTERACTING WITH GRASS CARP REOVIRUS VP39 PROTEIN BY PHAGE DISPLAY TECHNOLOGY

VP39 is a protein encoded by S9 gene of type Ⅲ grass carp reovirus (GCRV-Ⅲ). In order to study the biological function of VP39 protein in the process of GCRV infection of grass carp cells, the sequence of VP39 gene was cloned and the prokaryotic expression vector PET32A-VP39 was constructed. The fusion protein VP39-HIS was obtained by using prokaryotic expression method. Mouse anti-VP39 polyclonal antibody was prepared by immunizing mice with VP39 solution protein, and the antibody was evaluated by Western Blot. The polyclonal antibody was used to investigate the expression dynamics of VP39 protein in GCRV infected cells. The results of SDS-PAGE showed that the fusion protein of vp39-his was well soluble in PBS and the protein size was about 39 kDa. Western Blot analysis showed that the prepared VP39 polyclonal antibody could recognize both the prokaryotic expression of VP39-HIS fusion protein and the expression of VP39 protein after GCRV infection with CIK cells at the dilution ratio of 1﹕10000, showing good titer and specificity. In the process of virus infection, the expression of VP39 was low in the early stage and high in the middle and late stage. Two peptides were screened by phage display technology for specific binding to VP39 protein, and further bioinformatics analysis also found that 7 genes in grass carp genome had homology with the peptide, indicating that these genes may interact with VP39. In this study, mouse anti-VP39 polyclonal antibody was prepared, which provided a new immunological method for GCRV-Ⅲ detection. The screening of binding peptides also laid a foundation for the study of the biological function of VP39 in the process of GCRV infection.