Dizdaroglu M, Jaruga P, Rodriguez H
Chemical Science and Technology Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899-8311, USA.
Nucleic Acids Res. 2001 Feb 1;29(3):E12. doi: 10.1093/nar/29.3.e12.
Measurement of 8-hydroxy-2'-deoxyguanosine (8-OH-dGuo) in DNA by high-performance liquid chromatography/mass spectrometry (LC/MS) was studied. A methodology was developed for separation by LC of 8-OH-dGuo from intact and modified nucleosides in DNA hydrolyzed by a combination of four enzymes: DNase I, phosphodiesterases I and II and alkaline phosphatase. The atmospheric pressure ionization-electrospray process was used for mass spectral measurements. A stable isotope-labeled analog of 8-OH-dGuo was used as an internal standard for quantification by isotope-dilution MS (IDMS). Results showed that LC/IDMS with selected ion-monitoring (SIM) is well suited for identification and quantification of 8-OH-dGuo in DNA at background levels and in damaged DNA. The sensitivity level of LC/IDMS-SIM was found to be comparable to that reported previously using LC-tandem MS (LC/MS/MS). It was found that approximately five lesions per 10(6) DNA bases can be detected using amounts of DNA as low as 2 microgram. The results also suggest that this lesion may be quantified in DNA at levels of one lesion per 10(6) DNA bases, or even lower, when more DNA is used. Up to 50 microgram of DNA per injection were used without adversely affecting the measurements. Gas chromatography/isotope-dilution MS with selected-ion monitoring (GC/IDMS-SIM) was also used to measure this compound in DNA following its removal from DNA by acidic hydrolysis or by hydrolysis with Escherichia coli Fpg protein. The background levels obtained by LC/IDMS-SIM and GC/IDMS-SIM were almost identical. Calf thymus DNA and DNA isolated from cultured HeLa cells were used for this purpose. This indicates that these two techniques can provide similar results in terms of the measurement of 8-OH-dGuo in DNA. In addition, DNA in buffered aqueous solution was damaged by ionizing radiation at different radiation doses and analyzed by LC/IDMS-SIM and GC/IDMS-SIM. Again, similar results were obtained by the two techniques. The sensitivity of GC/MS-SIM for 7,8-dihydro-8-oxoguanine was also examined and found to be much greater than that of LC/MS-SIM and the reported sensitivity of LC/MS/MS for 8-OH-dGuo. Taken together, the results unequivocally show that LC/IDMS-SIM is well suited for sensitive and accurate measurement of 8-OH-dGuo in DNA and that both LC/IDMS-SIM and GC/IDMS-SIM can provide similar results.
研究了采用高效液相色谱/质谱联用(LC/MS)法测定DNA中的8-羟基-2'-脱氧鸟苷(8-OH-dGuo)。开发了一种方法,通过液相色谱从经四种酶(脱氧核糖核酸酶I、磷酸二酯酶I和II以及碱性磷酸酶)组合水解的DNA中的完整和修饰核苷中分离8-OH-dGuo。采用大气压电离-电喷雾过程进行质谱测量。使用8-OH-dGuo的稳定同位素标记类似物作为内标,通过同位素稀释质谱法(IDMS)进行定量。结果表明,采用选择离子监测(SIM)的LC/IDMS非常适合在背景水平和受损DNA中鉴定和定量DNA中的8-OH-dGuo。发现LC/IDMS-SIM的灵敏度水平与先前使用液相色谱串联质谱(LC/MS/MS)报道的相当。发现使用低至2微克的DNA量,每10⁶个DNA碱基中大约五个损伤可以被检测到。结果还表明,当使用更多DNA时,这种损伤在DNA中可以以每10⁶个DNA碱基一个损伤甚至更低的水平进行定量。每次进样使用高达50微克的DNA,且不会对测量产生不利影响。气相色谱/同位素稀释质谱联用选择离子监测(GC/IDMS-SIM)也用于在通过酸性水解或用大肠杆菌Fpg蛋白水解从DNA中去除该化合物后测量DNA中的这种化合物。通过LC/IDMS-SIM和GC/IDMS-SIM获得的背景水平几乎相同。为此使用了小牛胸腺DNA和从培养的HeLa细胞中分离的DNA。这表明这两种技术在测量DNA中的8-OH-dGuo方面可以提供相似的结果。此外,缓冲水溶液中的DNA在不同辐射剂量下受到电离辐射损伤,并通过LC/IDMS-SIM和GC/IDMS-SIM进行分析。同样,这两种技术获得了相似的结果。还检查了GC/MS-SIM对7,8-二氢-8-氧代鸟嘌呤的灵敏度,发现其远高于LC/MS-SIM以及报道的LC/MS/MS对8-OH-dGuo的灵敏度。综上所述,结果明确表明LC/IDMS-SIM非常适合灵敏且准确地测量DNA中的8-OH-dGuo,并且LC/IDMS-SIM和GC/IDMS-SIM都可以提供相似的结果。