Objective     To screen rhEndoglin-binding peptides from phage displayed 12-peptide library.      Methods     The rhEndoglin was used as target protein for biopanning of phage-displayed 12-peptide library. After three rounds of screening

16 phage clones were randomly selected and identified by sandwich ELISA. The positive phage clones were sequenced

and the fuse peptides were deduced by the DNA sequence. Further we identified the affinity and speciality by competitive inhibition test.      Results     Six of 16 phage clones were identified as positive clones by competent ELISA which could bind to rhEndoglin. Five sequences were obtained

and the amino acid sequence in two of these five was AHKHVHHVPVRL.      Conclusion     The rhEndoglin-binding peptides can be obtained by screening phage random peptide library. It could play an important role in early diagnosis of ovarian cancer.