Podmore I D, Cooper D, Evans M D, Wood M, Lunec J
Oxidative Stress Group, Division of Chemical Pathology, Leicester, LE2 7LX, United Kingdom.
Biochem Biophys Res Commun. 2000 Nov 2;277(3):764-70. doi: 10.1006/bbrc.2000.3752.
An assay with high selectivity and sensitivity has been developed which, for the first time, allows quantitative, simultaneous measurement in DNA of both 8-oxo-2'-deoxyguanosine (8-oxodG) and 8-oxo-2'-deoxyadenosine (8-oxodA)-important biomarkers of oxidative DNA damage in vivo. Using reversed-phase HPLC coupled to electrospray tandem mass spectrometry (HPLC-MS/MS) in multiple reaction monitoring (MRM) mode it was possible to detect background levels of these lesions in commercially available calf thymus DNA (85 +/- 3 and 7.1 +/- 0.2 per 10(6) DNA bases for 8-oxodG and 8-oxodA respectively; n = 3). Levels of 8-oxodG determined by HPLC coupled to an electrochemical detection system (HPLC-EC) were found to be similar (75 +/- 6 per 10(6) DNA bases; n = 3) to those obtained using tandem mass spectrometry.
已开发出一种具有高选择性和灵敏度的检测方法,该方法首次能够对体内氧化DNA损伤的重要生物标志物8-氧代-2'-脱氧鸟苷(8-oxodG)和8-氧代-2'-脱氧腺苷(8-oxodA)在DNA中进行定量、同时测量。使用反相高效液相色谱-电喷雾串联质谱联用仪(HPLC-MS/MS)在多反应监测(MRM)模式下,可以检测市售小牛胸腺DNA中这些损伤的背景水平(8-oxodG和8-oxodA分别为每10⁶个DNA碱基85±3和7.1±0.2;n = 3)。通过高效液相色谱-电化学检测系统(HPLC-EC)测定的8-oxodG水平与使用串联质谱法获得的水平相似(每10⁶个DNA碱基75±6;n = 3)。