摘要:变异型兔出血症病毒(Rabbit hemorrhagic disease virus variant,RHDV2)VP60蛋白是免疫保护性抗原,在诱导抗病毒感染的免疫反应中发挥重要作用。本实验以质粒pMD19-T-VP60-2为模板,PCR扩增获取VP60基因的主要抗原序列。然后用DNase I随机消化PCR产物,T4 DNA聚合酶补平,连接pEcoR I Linker和EcoR I酶切,以获取EcoR I识别的黏性末端。同时用pEcoR I酶切pC89 pⅧ型噬菌粒载体并进行去磷酸化处理。Microcon超滤装置回收20-125bp带有黏性末端的随机片段,并与pC89噬菌粒载体进行连接。将重组噬菌粒转化XL1-Blue感受态细胞,用辅助噬菌体VCSM13超感染,使制备的随机片段以融合蛋白形式展示于噬菌体表面,从而构建了RHDV2基因特异性噬菌体展示肽库。测定肽库滴度。结果显示所建肽库滴度约为3.5×1012PFU/mL,可以满足VP60抗原表位的筛选。27471 毕业论文关键词:变异型兔出血症病毒;VP60基因;特异性噬菌体展示肽库
Construction of VP60 Gene - specific Phage Peptide Library for Rabbit Hemorrhagic Disease Virus Variant(RHDV2)
Abstract:Variant Rabbit hemorrhagic disease virus (RHDV2) VP60 protein is an immune protective antigen that plays an important role in antiviral infection. In this study, VP60 gene was amplified by PCR using plasmid pMD19-T-VP60-2 as template. The PCR product was randomly digested by DNase I, catalyzed by T4 DNA polymerase to generate blunt ends, ligated with pEcoR I Linker and followed by EcoR I digestion to obtain the EcoR I–recognized viscous ends. The pC89-pVIII phagemid vector was digested with pEcoR I and subjected to dephosphorylation. The random fragments of 20-125bp with sticky ends were purified by the Microcon ultrafiltration device and were inserted into the pC89 phagemid vector. The recombinant phagemids was transformed into XL1-Blue competent cells and superimposed with the helper phage VCSM13. Obtained random fragments were expressed on the phage surface in form of fusion proteins, and thus the RHDV2 gene specific phage display peptide library was constructed. The peptide titer was determined. The results showed that the titer of the peptides was about 3.5×1012PFU/mL, which could be used to screen the VP60 epitopes.
Key words: RHDV2;VP60;Gene-specific phage peptide library
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