Identification and cloning of a trypsin inhibitor from skin secretions of Chinese red-belly toad Bombina maxima

Abstract

A novel trypsin inhibitor was identified and purified from skin secretions of Chinese red-belly toad Bombina maxima. The partial N-terminal 29 amino acid residues of the peptide, named BMTI, were determined by automated Edman degradation. This allowed the cloning of a full-length cDNA encoding BMTI from a cDNA library prepared from the toad skin. The deduced complete amino acid sequence of BMTI indicates that mature BMTI is composed of 60 amino acids. A fasta search in the databanks revealed that BMTI exhibits 81.7% sequence identity with BSTI, a trypsin/thrombin inhibitor from European toad Bombina bombina skin secretions. Sequence differences between BMTI and BSTI were due to 11 substitutions at positions 2, 9, 25, 27, 36–37, 39, 41–42, 50 and 56. BMTI potently inhibited trypsin with a K i value of 0.06 μM, similar to that of BSTI. However, unlike BSTI, which also inhibited thrombin with a K i value of 1 μM, no inhibitory effect of BMTI on thrombin was observed under the assay conditions.