Abstract
Highly reactive hydroxyl radical (OH) is generated during reaction of Cu,Zn-SOD (SOD) 1 with H 2 0 2 , its own enzymatic reaction product (SOD plus 0;-). During inactivation of Cu,Zn-SOD with H 2 0 2 , Cu 2 + liberated from the SOD catalyzes the formation of OH from H 2 0 2 . The OH thus generated will react with a,-protease inhibitor (a,-PI) if it is available in the milieu. To circumvent OH generation, we prepared eight different polymer-SOD conjugates and compared their stability against H 2 0 2 treatment. Furthermore, the effect of each polymer-SOD conjugate on a,-PI in the presence of H 2 0 2 was tested. Most polymer-SOD conjugates, except poly(styrene-co-maleic acid butylate; SMA)-SOD and poly(ethylene glycol; PEG)-SOD, showed higher stability than native SOD against inactivation by H 2 0 2 . The residual activity of divinylether maleic acid/anhydride copolymer (pyran copolymer)-conjugated SOD was 87% of the initial activity after incubation with 0.1 mM H 2 0 2 for 2 h, whereas that of native SOD was 49%. Antiprotease activity of ca,-PI was completely abrogated when the inhibitor was treated with native SOD and 3.0 mM H 2 0 2 , but there was no change with pyran copolymer-SOD after 3 h of incubation with H 2 0 2 . Our results suggest that pyran copolymer captured loosely bound Cu 2 + during the reaction of SOD with H 2 0 2 , thus resulting in suppression of both 0OH-mediated inactivation of SOD and suppression of activity of a,-PI. PEG showed little Cu 2 +-binding activity; no appreciable protection of SOD and a,-PI against OH generation was observed when Cu,Zn-SOD was conjugated with PEG. Circular dichroism and electron spin resonance studies of Cu,Zn-SOD treated with H 2 0 2 indicated that the peptide conformation as well as the copper ligand of Cu,Zn-SOD can be stabilized not only by pyran copolymer per se but also by conjugation of Cu,Zn-SOD with some copolymers such as pyran.
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Publication Info
- Year
- 1996
- Type
- article
- Volume
- 11
- Issue
- 3
- Pages
- 169-190
- Citations
- 26
- Access
- Closed
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Identifiers
- DOI
- 10.1177/088391159601100301