Screening for DNA adducts by data-dependent constant neutral loss-triple stage mass spectrometry with a linear quadrupole ion trap mass spectrometer

Erin E. Bessette, Angela K. Goodenough, Sophie Langouët, Isil Yasa, Ivan D. Kozekov, Simon D. Spivack, Robert J. Turesky

Research output: Contribution to journalArticle

58 Scopus citations

Abstract

A two-dimensional linear quadrupole ion trap mass spectrometer (LIT/MS) was employed to simultaneously screen for DNA adducts of environmental, dietary, and endogenous genotoxicants, by data-dependent constant neutral loss scanning followed by triple-stage mass spectrometry (CNL-MS 3). The loss of the deoxyribose (dR) from the protonated DNA adducts ([M + H - 116] +) in the MS/MS scan mode triggered the acquisition of MS 3 production spectra of the aglycone adducts [BH 2] +. Five DNA adducts of the tobacco carcinogen 4-aminobiphenyl (4-ABP) were detected in human hepatocytes treated with 4-ABP, and three DNA adducts of the cooked-meat carcinogen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) were identified in the livers of rats exposed to MeIQx, by the CNL-MS 3 scan mode. Buccal cell DNA from tobacco smokers was screened for DNA adducts of various classes of carcinogens in tobacco smoke including 4-ABP, 2-amino-9H-pyrido[2,3- b]indole (AαC), and benzo[a]pyrene (BaP); the cooked-meat carcinogens MeIQx, AαC, and 2-amino-1-methyl-6-phenylmidazo[4,5-b]pyridine (PhIP); and the lipid peroxidation products acrolein (AC) and trans-4-hydroxynonenal (HNE). The CNL-MS 3 scanning technique can be used to simultaneously screen for multiple DNA adducts derived from different classes of carcinogens, at levels of adduct modification approaching 1 adduct per 10 8 unmodified DNA bases, when 10 μg of DNA is employed for the assay.

Original languageEnglish (US)
Pages (from-to)809-819
Number of pages11
JournalAnalytical Chemistry
Volume81
Issue number2
DOIs
StatePublished - Jan 15 2009

ASJC Scopus subject areas

  • Analytical Chemistry

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