Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs
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Data
2002-01-01
Autores
Nakaie, C. R.
Silva, E. G.
Cilli, Eduardo Maffud [UNESP]
Marchetto, Reinaldo [UNESP]
Schreier, S.
Paiva, T. B.
Paiva, ACM
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Título de Volume
Editor
Elsevier B.V.
Resumo
Angiotensin II (AngII) and bradykinin (BK) derivatives containing the TOAC (2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid) spin label were synthesized by solid phase methodology. Ammonium hydroxide (pH 10, 50degreesC, 1 h) was the best means for reverting nitroxide protonation occurring during peptide cleavage. EPR spectra yielded rotational correlation times for internally labeled analogs that were nearly twice as large as those of N-terminally labeled analogs. Except for TOAC(1)-AngII and TOAC(0)-BK, which showed high intrinsic activities, other derivatives were inactive in smooth muscle preparations. These active paramagnetic analogs may be useful for conformational studies in solution and in the presence of model and biological membranes. (C) 2002 Elsevier B.V. All rights reserved.
Descrição
Palavras-chave
angiotensin analogs, bradykinin analogs, peptide synthesis, spin labeled peptides, TOAC spin label, electron paramagnetic resonance
Como citar
Peptides. New York: Elsevier B.V., v. 23, n. 1, p. 65-70, 2002.