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570537 
Journal Article 
Oxidation of 5-thio-2-nitrobenzoic acid, by the biologically relevant oxidants peroxynitrite anion, hydrogen peroxide and hypochlorous acid 
Landino, LM; Mall, CB; Nicklay, JJ; Dutcher, SK; Moynihan, KL 
2008 
1 
Nitric Oxide
ISSN: 1089-8603
EISSN: 1089-8611 
18 
1 
11-18 
English 
18023374 
WOS:000252608600002 
The modification of protein and non-protein thiols by oxidants including hydrogen peroxide (H2O2), peroxynitrite anion (ONOO-) and hypochlorous acid (HOCl) is well documented. Using an aromatic thiol, 5-thio-2-nitrobenzoic acid, and biologically relevant oxidants, we have identified higher oxidation states of sulfur including the sulfonic acid derivative and the disulfide S-oxide, a thiosulfinate, by HPLC and mass spectrometry. The initial reaction of ONOO- with 5-thio-2-nitrobenzoic acid yielded a transient red intermediate, the sulfenate anion. The red intermediate was observed when ONOO- and H2O2 were used to oxidize 5-thio-2-nitrobenzoic acid and it persisted for several seconds at pH 7. HOCl oxidized the disulfide, 5,5'dithiobis(2-nitrobenzoic acid) to the corresponding sulfonic acid and no additional products were detected. Using this system, we can directly compare the thiol-oxidizing abilities of several oxidants. Because 5-thio-2-nitrobenzoic acid is the product of the reaction of Ellman's reagent with protein thiols, a detailed study of its stability in biological matrices where oxidants may be generated is warranted. 
Thiol; Peroxynitrite; Reactive sulfur species; Sulfenic acid; Thiosulfinate; Sulfonic acid