Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin 1-converting enzyme

Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin 1-converting enzyme

Author Teixeira, Luis Gustavo de Deus Autor UNIFESP Google Scholar
Bersanetti, Patricia Alessandra Autor UNIFESP Google Scholar
Schreier, Shirley Google Scholar
Carmona, Adriana Karaoglanovich Autor UNIFESP Google Scholar
Nakaie, Clovis Ryuichi Autor UNIFESP Google Scholar
Institution Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Abstract The angiotensin I-converting enzyme (ACE) converts the decapeptide angiotensin I (Ang I) into angiotensin II by releasing the C-terminal dipeptide. A novel approach combining enzymatic and electron paramagnetic resonance (EPR) studies was developed to determine the enzyme effect on Ang I containing the paramagnetic 2,2,6,6-tetramethylpiperidine-1-oxyl-4-amino-4-carboxylic acid (TOAC) at positions 1, 3, 8, and 9. Biological assays indicated that TOAC(1)-Ang I maintained partly the Ang I activity, and that only this derivative and the TOAC(3)-Ang I were cleaved by ACE. Quenching of Tyr(4) fluorescence by TOAC decreased with increasing distance between both residues, suggesting an overall partially extended structure. However, the local bend known to be imposed by the substituted diglycine TOAC is probably responsible for steric hindrance, not allowing the analogues containing TOAC at positions 8 and 9 to act as substrates. in some cases, although substrates and products differ by only two residues, the difference between their EPR spectral lineshapes allows monitoring the enzymatic reaction as a function of time. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Keywords peptides
angiotensins
angiotensin I-converting
enzyme
TOAC
electron spin resonance spectroscopy
enzymes
Language English
Date 2007-05-29
Published in Febs Letters. Amsterdam: Elsevier B.V., v. 581, n. 13, p. 2411-2415, 2007.
ISSN 0014-5793 (Sherpa/Romeo, impact factor)
Publisher Elsevier B.V.
Extent 2411-2415
Origin http://dx.doi.org/10.1016/j.febslet.2007.04.058
Access rights Open access Open Access
Type Article
Web of Science ID WOS:000247087600005
URI http://repositorio.unifesp.br/handle/11600/29754

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