Identification of bradykinin: related peptides from Phyllomedusa nordestina skin secretion using electrospray ionization tandem mass spectrometry after a single-step liquid chromatography
2009
Conceição, K(CEPID Center for Applied Toxinology Special Laboratory of Applied Toxinology) | Bruni, FM(CEPID Center for Applied Toxinology Special Laboratory of Applied Toxinology) | Sciani, JM(Butantan Institute Laboratory of Biochemistry and Biophysics) | Konno, K(CEPID Center for Applied Toxinology Special Laboratory of Applied Toxinology) | Melo, RL(CEPID Center for Applied Toxinology Special Laboratory of Applied Toxinology) | Antoniazzi, MM(CEPID Center for Applied Toxinology Laboratory of Cell Biology) | Jared, C(CEPID Center for Applied Toxinology Laboratory of Cell Biology) | Lopes-Ferreira, M(CEPID Center for Applied Toxinology Special Laboratory of Applied Toxinology) | Pimenta, DC(Butantan Institute Laboratory of Biochemistry and Biophysics)
Amphibian skin secretions are a source of potential new drugs with medical and biotechnological applications. Rich in peptides produced by holocrine-type serous glands in the integument, these secretions play different roles, either in the regulation of physiological skin functions or in the defense against predators or microorganisms. The aim of the present work was to identify novel peptides with bradykinin-like structure and/or activity present in the skin of Phyllomedusa nordestina. In order to achieve this goal, the crude skin secretion of this frog was pre-fractionated by solid phase extraction and separated by reversed-phase chromatography. The fractions were screened for low-molecular-mass peptides and sequenced by mass spectrometry. It was possible to identify three novel bradykinin-related peptides, namely: KPLWRL-NH2 (Pnor 3), RPLSWLPK (Pnor 5) and VPPKGVSM (Pnor 7) presenting vascular activities as assessed by intravital microscopy. Pnor 3 and Pnor 7 were able to induce vasodilation. On the other hand, Pnor 5 was a potent vasoconstrictor. These effects were reproduced by their synthetic analogues.
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