A comprehensive proteomic study of the skin secretions of the frog lithobates spectabilis

Disulfide c-terminal loop fragments derived from amps and the presence of peptidases have been previously reported in the skin secretions of different amphibians. however,there are only a few studies on the identification of enzymes in frog skin secretion based on the primary structure of these proteins. similarly,little data exist regarding the identification of disulfide c-terminal loops at large scale. therefore,a comprehensive study on this issue certainly could bring in much more information for understanding this molecular process and its biochemical consequences. thus,the aim of this work was to characterize the presence of disulfide c-terminal loop fragments of amps and identify the proteins and probable enzymes present in the completely unknown secretion contents of the frog lithobates spectabilis. for this purpose,high-resolution mass spectrometry was applied to analyze the skin secretions processed by two different protocols: (1) using a cocktail of enzymatic inhibitors and 2) without any protease inhibitors,maintaining the solution for 2 hours at 10° c. results from procedure-1,revealed 122 molecular masses,whereas procedure-2 permitted 253 different molecular masses to be identified. fifty-nine peptides including 22 disulfide c-terminal loop-containing peptides were obtained following procedure-2. polyacrylamide gel electrophoresis separation,tryptic digestion and lc-ms/ms were used for de novo sequencing of 111 different peptides and the unequivocal identification of fifteen proteins including at least three different peptidases. additionally,it was possible to fully sequence eight peptides,including a ranatuerin-related peptide identified here as spectabilin,that was subsequently chemically synthesized and showed high antibacterial,antiparasitic and cytotoxic activities. © 2016 bentham science publishers.