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Objective: The major capsid protein CP2 of Taura syndrome virus (TSV) was cloned and expressed, peptides binding to CP2 were successfully obtained from a phage display random dodecapeptide library.Methods: According to the nucleotide sequence of recombinant plasmid pMD-CP2, a pair of primer was designed to amplify the high variable region 376~1371bp of CP2 gene.The product was purified and cloned into the prokaryotic vector pET-32a to construct the recombinant plasmid,designated pET-CP2.