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J Biol Chem ; 275(15): 10745-53, 2000 Apr 14.
Artigo em Inglês | MEDLINE | ID: mdl-10753865

RESUMO

Vasostatin-1, the natural N-terminal 1-76 chromogranin A (CGA)-derived fragment in bovine sequence, has been purified from chromaffin secretory granules and identified by sequencing and matrix-assisted laser desorption time-of-flight mass spectrometry. This peptide, which displays antibacterial activity against Gram-positive bacteria at micromolar concentrations, is also able to kill a large variety of filamentous fungi and yeast cells in the 1-10 microM range. We have found that the C-terminal moiety of vasostatin-1 is essential for the antifungal activity, and shorter active peptides have been synthesized. In addition, from the comparison with the activity displayed by related peptides (human recombinant and rat synthetic fragments), we could determine that antibacterial and antifungal activities have different structural requirements. To assess for such activities in vivo, CGA and CGA-derived fragments were identified in secretory material released from human polymorphonuclear neutrophils upon stimulation. Vasostatin-1, which is stored in a large variety of cells (endocrine, neuroendocrine, and neurons) and which is liberated from stimulated chromaffin and immune cells upon stress, may represent a new component active in innate immunity.


Assuntos
Anti-Infecciosos/farmacologia , Bactérias/efeitos dos fármacos , Cromograninas/farmacologia , Fungos/efeitos dos fármacos , Fragmentos de Peptídeos/farmacologia , Sequência de Aminoácidos , Animais , Antibacterianos , Bovinos , Cromogranina A , Humanos , Dados de Sequência Molecular , Neutrófilos/metabolismo , Ratos , Proteínas Recombinantes/farmacologia , Relação Estrutura-Atividade
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