Is ascorbate able to reduce disulfide bridges? A cautionary note

被引:98
作者
Giustarini, Daniela [1 ]
Dalle-Donne, Isabella [2 ]
Colombo, Roberto [2 ]
Milzani, Aldo [2 ]
Rossi, Ranieri [1 ]
机构
[1] Univ Siena, Dept Evolut Biol, Lab Pharmacol & Toxicol, I-53100 Siena, Italy
[2] Univ Milan, Dept Biol, I-20133 Milan, Italy
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2008年 / 19卷 / 03期
关键词
S-Nitrosothiols; Nitric oxide; Ascorbate; Biotin switch assay;
D O I
10.1016/j.niox.2008.07.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The biotin switch assay has recently been proposed as the eligible method to identify different S-nitrosated proteins in biological matrices. However, notwithstanding its wide application, a thorough validation of this method is still lacking. In particular, it has been suggested that ascorbate concentrations higher than 1 mM (as proposed in the original method) are needed since ascorbate reaction with S-nitrosothiols is slow. But the selectivity of ascorbate as a cleaving agent of the S-N bond under these conditions has not been well characterized. Our data indicate that ascorbate is able to reduce disulfide bridges of DTNB, cystine, cystinylglycine, glutathione disulfide, protein mixed disuffides and biotin-HPDP with pH and concentration dependent rates. Additionally, we tested the effect of indirect sunlight on ascorbate-mediated cleavage of both disulfides and S-nitrosothiols. (c) 2008 Elsevier Inc. All rights reserved.
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页码:252 / 258
页数:7
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