The fragment of the 1-methylpyrene cation, is expected to exist in two isomeric forms, 1-pyrenemethylium and the tropylium containing species We measured the infrared (IR) action spectrum of cold tagged with Ne using a cryogenic ion trap instrument coupled to the FELIX laser. Comparison of the experimental data with density functional theory calculations allows us to identify the isomer in our experiments. The IR Multi-Photon Dissociation spectrum was also recorded following the CH loss channel. Its analysis suggests combined effects of anharmonicity and isomerisation while heating the trapped ions, as shown by molecular dynamics simulations.
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http://dx.doi.org/10.1016/j.cplett.2018.03.028 | DOI Listing |
Arch Toxicol
February 2021
Department of Toxicology, School of Public Health, Southern Medical University, 1023 S. Shatai Road, Guangzhou, 510515, China.
1-Methylpyrene (1-MP) is a common environmental pollutant and animal carcinogen. After sequential activation by cytochromes P450 and sulfotransferases, it induced gene mutations and micronuclei in mammalian cells. The type of micronuclei formed, entire chromosomes or fragments, was not analysed.
View Article and Find Full Text PDFChem Phys Lett
April 2018
Institut de Recherche en Astrophysique et Planétologie (IRAP), Université de Toulouse (UPS), CNRS, CNES, 9 Av. du Colonel Roche, 31028 Toulouse Cedex 4, France.
The fragment of the 1-methylpyrene cation, is expected to exist in two isomeric forms, 1-pyrenemethylium and the tropylium containing species We measured the infrared (IR) action spectrum of cold tagged with Ne using a cryogenic ion trap instrument coupled to the FELIX laser. Comparison of the experimental data with density functional theory calculations allows us to identify the isomer in our experiments. The IR Multi-Photon Dissociation spectrum was also recorded following the CH loss channel.
View Article and Find Full Text PDFChem Res Toxicol
October 2008
Department of Toxicology, German Institute of Human Nutrition (DIfE), 14558 Nuthetal, Germany.
The alkylated polycyclic aromatic hydrocarbon 1-methylpyrene is a carcinogen in rodents and has been detected in various environmental matrices and foodstuffs. It is activated metabolically by benzylic hydroxylation to 1-hydroxymethylpyrene followed by sulfoconjugation to yield electrophilic 1-sulfooxymethylpyrene (1-SMP) that is prone to form DNA adducts. An LC-MS/MS method using multiple reaction monitoring (MRM) of fragment ions has been developed for specific detection and quantification of N (2)-(1-methylpyrenyl)-2'-deoxyguanosine (MP-dGuo) and N (6)-(1-methylpyrenyl)-2'-deoxyadenosine (MP-dAdo) formed in DNA in the presence of 1-SMP.
View Article and Find Full Text PDFCarcinogenesis
April 1993
Ben May Institute, University of Chicago, IL 60637.
Twenty-eight base complementary oligonucleotides were synthesized with deoxyadenosine residues modified at the N6 position with 1-methylpyrene (MP) specifically positioned 3 bp apart in opposite DNA strands. Doubly modified constructs as well as non-modified and singly modified constructs were ligated into M13mp19 and an SV40-based shuttle vector pSVL-lac for transfection into Escherichia coli and large T-antigen-expressing monkey kidney epithelial cells respectively. Repair of MP adducts was analyzed by direct nucleotide sequencing after selection of clones containing the 28mer construct.
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