Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1216183 | Journal of Chromatography B | 2007 | 12 Pages |
Abstract
S-Nitrosothiol (SNO) cysteine modifications are regulated signaling reactions that dramatically affect, and are affected by, protein conformation. The lability of the SNO bond can make SNO-modified proteins cumbersome to measure accurately. Here, we review methodologies for detecting SNO modifications in biology. There are three caveats. (1) Many assays for biological SNOs are used near the limit of detection: standard curves must be in the biologically relevant concentration range. (2) The assays that are most reliable are those that modify SNO protein or peptide chemistry the least. (3) Each result should be quantitatively validated using more than one assay. Improved assays are needed and are in development.
Related Topics
Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Andrew Gow, Allan Doctor, Joan Mannick, Benjamin Gaston,