Your browser doesn't support javascript.
loading
Identification of bradykinin: related peptides from Phyllomedusa nordestina skin secretion using electrospray ionization tandem mass spectrometry after a single-step liquid chromatography
Conceição, K; Bruni, F. M; Sciani, J. M; Konno, K; Melo, R. L; Antoniazzi, M. M; Jared, C; Lopes-Ferreira, M; Pimenta, D. C.
  • Conceição, K; Center for Applied Toxinology. Special Laboratory of Applied Toxinology. São Paulo. BR
  • Bruni, F. M; Center for Applied Toxinology. Special Laboratory of Applied Toxinology. São Paulo. BR
  • Sciani, J. M; Butantan Institute. Laboratory of Biochemistry and Biophysics. São Paulo. BR
  • Konno, K; Center for Applied Toxinology. Special Laboratory of Applied Toxinology. São Paulo. BR
  • Melo, R. L; Center for Applied Toxinology. Special Laboratory of Applied Toxinology. São Paulo. BR
  • Antoniazzi, M. M; Center for Applied Toxinology. Laboratory of Cell Biology. São Paulo. BR
  • Jared, C; Center for Applied Toxinology. Laboratory of Cell Biology. São Paulo. BR
  • Lopes-Ferreira, M; Center for Applied Toxinology. Special Laboratory of Applied Toxinology. São Paulo. BR
  • Pimenta, D. C; Butantan Institute. Laboratory of Biochemistry and Biophysics. São Paulo. BR
J. venom. anim. toxins incl. trop. dis ; 15(4): 633-652, 2009. ilus, tab
Article in English | LILACS | ID: lil-532750
ABSTRACT
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.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Anura / Peptides / Bradykinin Type of study: Diagnostic study Limits: Animals Language: English Journal: J. venom. anim. toxins incl. trop. dis Journal subject: Toxicology Year: 2009 Type: Article Affiliation country: Brazil Institution/Affiliation country: Butantan Institute/BR / Center for Applied Toxinology/BR

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: LILACS (Americas) Main subject: Anura / Peptides / Bradykinin Type of study: Diagnostic study Limits: Animals Language: English Journal: J. venom. anim. toxins incl. trop. dis Journal subject: Toxicology Year: 2009 Type: Article Affiliation country: Brazil Institution/Affiliation country: Butantan Institute/BR / Center for Applied Toxinology/BR