413567-58-5Relevant academic research and scientific papers
Modified immunoenriched 32P-HPLC assay for the detection of O4-ethylthymidine in human biomonitoring studies
Godschalk, Roger,Nair, Jagadeesan,Kliem, Hans-Christian,Wiessler, Manfred,Bouvier, Guy,Bartsch, Helmut
, p. 433 - 437 (2007/10/03)
Increased excretion of ethylated DNA bases has been reported in the urine of cigarette smokers. To study DNA ethylation in the target organs of smokers, an immunoenriched 32P-postlabeling assay for O4-ethylthymidine (O4-etT) was developed. O4-etT-3′-monophosphate (O4-etT-3′P) was synthesized, purified, and characterized by LC-MS, ESI-MS, and NMR. DNA was enzymatically digested to 2′-deoxynucleoside-3′-monophosphate followed by immunoprecipitation of O4-etT-3′P using specific monoclonal antibodies. The immunoconjugate was washed by filtration, and O4-etT-3′P was recovered by ethanol treatment. The enriched O4-etT-3′P was labeled with [γ-32P]ATP in the presence of T4-polynucleotide kinase at pH 6.8 to yield its 5′labeled monophosphate and was subsequently resolved on RP-HPLC and detected with online detection of radioactivity. Adduct recovery was > 80%, and the detection limit was approximately 500 amol. To further validate the method, O4-etT levels were determined in calf thymus DNA treated with N-ethyl-N-nitrosourea, and a dose-dependent formation of O4-etT was observed. Furthermore, O4-etT was found to be present in the cells obtained from the lower respiratory tract by sputum induction of two out of four smokers but not in three nonsmokers. O4-etT is a poorly repaired promutagenic DNA lesion; thus, it could be of potential use for biomonitoring smoking-related DNA damage. Our improved assay was found to be sufficiently sensitive and specific to detect O4-etT in surrogate cells from cigarette smoke exposed humans.
