Journal
PHARMACEUTICAL RESEARCH
Volume 20, Issue 4, Pages 684-692Publisher
KLUWER ACADEMIC/PLENUM PUBL
DOI: 10.1023/A:1023219420935
Keywords
human serum albumin; cysteine mutation; chloramine-T; Site II; oxidative damage; pharmacokinetics
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Purpose. The validity of using chloramine- T as a model compound for mimicing oxidative stress was examined using human serum albumin ( HSA) as a model. Important sites of oxidation were studied by mild treatment with chloramine- T and by mutating (34)Cys for a serine ( C34S). Methods. High- performance liquid chromatography ( HPLC) combined with fluorescence detection to confirm the validity of chloramine-T as an oxidizing agent was used. Oxidized amino acid residues were detected by reaction with 5,5 '- dithiobis( 2- nitro benzoic acid), digestion with cyanogen bromide, followed by capillary electrophoresis. Protein conformation was examined by spectroscopic techniques. Results. From the HPLC analysis of human serum, the validity of using chloramine- T as an oxidizing agent was confirmed. At low chloramine-T concentrations ( CT0.1- HSA, CT1- HSA), (34)Cys and Met residues were oxidized, at medium concentrations ( CT10- HSA), the tryptophan residue also appeared to be oxidized, and at the highest concentration ( CT50- HSA), the net charge of Site II of HSA was found to be more negative. The two highest levels of oxidation of HSA ( CT10- HSA, CT50- HSA) resulted in conformational changes with an increased exposure of hydrophobic regions, decreased high-affinity bindings of warfarin and ketoprofen and a reduced esterase-like activity. The latter protein also has a shorter plasma half- life and an increased liver clearance. Conclusions. We succeeded in imitating oxidative damage to HSA using chloramine- T and the findings show that Site II is more affected than Site I and (34)Cys, when HSA is exposed to oxidative stress.
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