Abstract
Advanced glycation end products (AGEs), which are composed of various glucose or carbohydrate adducts, are thought to be responsible for several diabetic and age-related complications. However, to date, specific sites on proteins that are modified by AGEs remain largely unknown. We report here the use of matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) to determine the type and localization of several AGEs formed in vitro on human beta-2-microglobulin (β 2M),and in vivo on type 2 ryanodine receptor calcium-release channel (RyR2), and sarco(endo)plasmic reticulum (SERCA2a). A PERL script algorithm, developed in-house, makes searching the relatively large amount of data generated by the MALDI-MS more manageable.The outstanding sensitivity of MALDI-TOF-MS coupled with the PERL script algorithm allows such an approach to be a very useful tool in detecting AGEs and other post-translational modifications. We believe that this method could be an important tool when searching for post-translational modifications on proteins.
Original language | English |
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Pages (from-to) | 224-230 |
Number of pages | 7 |
Journal | Journal of Biomolecular Techniques |
Volume | 14 |
Issue number | 3 |
Publication status | Published - Sept 2003 |
Externally published | Yes |
Keywords
- Advanced-glycation end products
- Mass spectrometry
- Matrix-assisted laser desorption/ionization
- Post-translational modification