Journal of Molecular Catalysis A-Chemical, Vol.269, No.1-2, 225-233, 2007
N-bromosuccinimide assisted oxidation of hydrophobic tetrapeptide sequences of elastin: A mechanistic study
The repeating sequences of elastin, glycyl-glycyl-alanyl-proline (GGAP) glycyl-glycyl-isoleucyl-proline (GGIP) and more hydrophobic glycyl-glycyl-phenylalanyl-proline (GGPP), were synthesized by classical solution phase methods and characterized. The kinetics of oxidation of tetrapeptides (TPs) and their constituent amino acids (AAs) by N-bromosuccinimide (NBS) was studied in the presence of perchlorate ions in acidic medium at 28 degrees C. The reaction was followed spectrophotometrically at gimel(max)=240 nm. The reactions follow identical kinetics, being first order each in [NBS], [AA] and TP]. No effect on the rate of [H+], reduction product [succinimide] and ionic strength was observed. Effects of dielectric constant of the medium and the added anions such as chloride and perchlorate were studied. Activation parameters have been computed. The oxidation products of the reaction were isolated and characterized. The proposed mechanism is consistent with the experimental results. An apparent correlation was noted between the rate of oxidation and the hydrophobicity of AAs and TPs. (c) 2007 Elsevier B.V. All rights reserved.