Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/62157
Type: Artigo de periódico
Title: Novel natural peptide substrates for endopeptidase 24.15, neurolysin, and angiotensin-converting enzyme
Author: Rioli, V
Gozzo, FC
Heimann, AS
Linardi, A
Krieger, JE
Shida, CS
Almeida, PC
Hyslop, S
Eberlin, MN
Ferro, ES
Abstract: Endopeptidase 24.15 (EC 3.4.24.15; ep24.15), neurolysin (EC 3.4.24.16; ep24.16), and angiotensin-converting enzyme (EC 3.4.15.1; ACE) are metallopepticlases involved in neuropeptide metabolism in vertebrates. Using catalytically inactive forms of ep24.15 and ep24.16, we have identified new peptide substrates for these enzymes. The enzymatic activity of ep24.15 and ep24.16 was inactivated by site-directed mutagenesis of amino acid residues within their conserved HEXXH motifs, without disturbing their secondary structure or peptide binding ability, as shown by circular dichroism and binding assays. Fifteen of the peptides isolated were sequenced by electrospray ionization tandem mass spectrometry and shared homology with fragments of intracellular proteins such as hemoglobin. Three of these peptides (PVNFKFLSH, VVYPWTQRY, and LVVYPWTQRY) were synthesized and shown to interact with ep24.15, ep24.16, and ACE, with K-i values ranging from 1.86 to 27.76 muM. The hemoglobin alpha-chain fragment PVNFKFLSH, which we have named hemopressin, produced dose-dependent hypotension in anesthetized rats, starting at 0.001 mug/kg. The hypotensive effect of the peptide was potentiated by enalapril only at the lowest peptide dose. These results suggest a role for hemopressin as a vasoactive substance in vivo. The identification of these putative intracellular substrates for ep24.15 and ep24.16 is an important step toward the elucidation of the role of these enzymes within cells.
Country: EUA
Editor: Amer Soc Biochemistry Molecular Biology Inc
Rights: fechado
Identifier DOI: 10.1074/jbc.M212030200
Date Issue: 2003
Appears in Collections:Unicamp - Artigos e Outros Documentos

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