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J. Biol. Chem., Vol. 269, Issue 48, 30200-30205, 12, 1994
CK Mukhopadhyay and IB Chatterjee
In this paper we demonstrate that in the absence of free metal ions, active
oxygen species, generated by activated macrophages or xanthine/xanthine
oxidase (XOD), carry out oxidative degradation of collagen fibrils type I
in conjunction with proteases. The collagen degradation is completely
prevented by ascorbate (AH2) but not by catalase. The free metal
ion-independent collagen degradation is a two- step process: (i) oxidation
of collagen and (ii) subsequent proteolytic cleavage of the oxidatively
modified collagen. AH2 completely prevents collagen oxidation and thereby
protects the collagen from subsequent proteolytic degradation. This is in
contrast to free metal ion- catalyzed spontaneous fragmentation of
collagen, which is accelerated by AH2 and inhibited by catalase (Kato, Y.,
Uchida, K., and Kawakishi, S. (1992) J. Biol. Chem. 267, 23646-23651).
Studies using xanthine/XOD and model polypeptides, namely, poly-L-Pro,
poly-L-hydroxyproline, poly- L-Lys, and poly(Pro-Gly-Pro) indicate that
although O2-. is needed along with XOD, oxidation of model polypeptides
appears to be a direct function of XOD iron, which is also stimulated by
cytochrome P450.
Free metal ion-independent oxidative damage of collagen. Protection by ascorbic acid
Department of Biochemistry, University College of Science, Calcutta, India.
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