Endogenous 3,4-Dihydroxyphenylalanine and Dopaquinone Modifications on Protein Tyrosine

• Published in: Molecular & cellular proteomics Vol. 9; no. 6; pp. 1199 - 1208
• Main Authors: Zhang, Xu, Monroe, Matthew E., Chen, Baowei, Chin, Mark H., Heibeck, Tyler H., Schepmoes, Athena A., Yang, Feng, Petritis, Brianne O., Camp, David G., Pounds, Joel G., Jacobs, Jon M., Smith, Desmond J., Bigelow, Diana J., Smith, Richard D., Qian, Wei-Jun
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 01.06.2010
• ISSN: 1535-9476; 1535-9484
• DOI: 10.1074/mcp.M900321-MCP200

Oxidative modifications of protein tyrosines have been implicated in multiple human diseases. Among these modifications, elevations in levels of 3,4-dihydroxyphenylalanine (DOPA), a major product of hydroxyl radical addition to tyrosine, has been observed in a number of pathologies. Here we report the first proteome survey of endogenous site-specific modifications, i.e. DOPA and its further oxidation product dopaquinone in mouse brain and heart tissues. Results from LC-MS/MS analyses included 50 and 14 DOPA-modified tyrosine sites identified from brain and heart, respectively, whereas only a few nitrotyrosine-containing peptides, a more commonly studied marker of oxidative stress, were detectable, suggesting the much higher abundance for DOPA modification as compared with tyrosine nitration. Moreover, 20 and 12 dopaquinone-modified peptides were observed from brain and heart, respectively; nearly one-fourth of these peptides were also observed with DOPA modification on the same sites. For both tissues, these modifications are preferentially found in mitochondrial proteins with metal binding properties, consistent with metal-catalyzed hydroxyl radical formation from mitochondrial superoxide and hydrogen peroxide. These modifications also link to a number of mitochondrially associated and other signaling pathways. Furthermore, many of the modification sites were common sites of previously reported tyrosine phosphorylation, suggesting potential disruption of signaling pathways. Collectively, the results suggest that these modifications are linked with mitochondrially derived oxidative stress and may serve as sensitive markers for disease pathologies.