Analysis of DNA-bound advanced glycation end-products by LC and mass spectrometry

J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Aug;855(1):51-8. doi: 10.1016/j.jchromb.2006.11.033. Epub 2006 Dec 11.

Abstract

Sugars and sugar degradation products readily react in vitro with guanine derivatives, resulting in the formation of DNA-bound advanced glycation end-products (DNA-AGEs). The two diastereomers of N(2)-(1-carboxyethyl)-2'-deoxyguanosine (CEdG(A,B)) and the cyclic adduct of methylglyoxal and 2'-deoxyguanosine (mdG) (N(2)-7-bis(1-hydroxy-2-oxopropyl)-2'-deoxyguanosine have also been detected in cultured cells and/or in vivo. LC-MS/MS methods have been developed to analyze sensitively DNA adducts in vitro and in vivo. In this paper, the chemical structures of possible DNA-AGEs and the application of LC-MS/MS to measure DNA-AGEs are reviewed.

Publication types

  • Review

MeSH terms

  • Animals
  • Chromatography, Liquid / methods*
  • DNA / chemistry*
  • DNA / metabolism
  • DNA Adducts / analysis
  • Glycation End Products, Advanced / analysis*
  • Glycation End Products, Advanced / urine
  • Humans
  • Mass Spectrometry / methods*

Substances

  • DNA Adducts
  • Glycation End Products, Advanced
  • DNA