Mass spectrometric methods for the analysis of nucleoside-protein cross-links: application to oxopropenyl-deoxyadenosine.

Abstract:

:Electrophilic DNA adducts produced following oxidative stress can form DNA-protein cross-links (DPCs), dramatically altering genomic maintenance pathways. Complete characterization of DPCs has been hindered, in part, because of a lack of comprehensive techniques for their analysis. We have, therefore, established a proteomics approach to investigate sites of cross-link formation using N(6)-(3-oxo-1-propenyl)-2'-deoxyadenosine (OPdA), an electrophilic DNA adduct produced from oxidative stress. OPdA was reacted with albumin and reduced with NaBH4 to stabilize DPCs. Using LC-MS/MS proteomics techniques, high-resolution peptide sequence data were obtained; however, using a database searching strategy, adducted peptides were only identified in samples subjected to chemical depurination. This strategy revealed multiple oxopropenyl adenine-lysine adducts and oxopropenyl-lysine adducts with the most reactive lysines identified to be Lys256 and Lys548. Manual interrogation of the mass spectral data provided evidence of OPdA deoxynucleoside conjugates to lysines and cross-links that underwent facile collision-induced dissociation to release an unmodified peptide without subsequent fragmentation. These fragmentations precluded adduct detection and peptide sequencing using database searching methods. Thus, comprehensive analysis of DPCs requires chemical depurination of DNA-protein reaction mixtures followed by a combination of database-dependent and manual interrogation of LC-MS/MS data using higher-energy collision-induced dissociation. In the present case, this approach revealed that OPdA selectively modifies surface lysine residues and produces nucleoside-protein cross-links and oxopropenyl lysine.

journal_name

Chem Res Toxicol

authors

Shuck SC,Rose KL,Marnett LJ

doi

10.1021/tx400384e

subject

Has Abstract

pub_date

2014-01-21 00:00:00

pages

136-46

issue

1

eissn

0893-228X

issn

1520-5010

journal_volume

27

pub_type

杂志文章
  • Low kinetic hydrogen isotope effects in the dehydrogenation of 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester (nifedipine) by cytochrome P-450 enzymes are consistent with an electron/proton/electron transfer mechan

    abstract::Cytochrome P-450 enzymes have been postulated to oxidize amines through a variety of mechanisms. One of the means of distinguishing among potential pathways involves the use of kinetic hydrogen isotope effects: low isotope effects are characteristic of aminium radical mechanisms while high values are consistent with h...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00013a004

    authors: Guengerich FP

    更新日期:1990-01-01 00:00:00

  • Induction of cytotoxicity, aldehydic DNA lesions, and poly(ADP-ribose) polymerase-1 activation by catechol derivatives of pentachlorophenol in calf thymus DNA and in human breast cancer cells.

    abstract::The purpose of this study was to investigate the degree of chlorination of catechol (CAT) derivatives of pentachlorophenol (PCP) on the induction of cytotoxicity and DNA damaging effects in calf thymus DNA (ct-DNA) and in two human breast carcinoma cell lines. Results indicated that with the addition of the transition...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0498511

    authors: Lin CH,Leow HT,Huang SC,Nakamura J,Swenberg JA,Lin PH

    更新日期:2005-02-01 00:00:00

  • In vitro metabolism of 2-acetylbenzothiophene: relevance to zileuton hepatotoxicity.

    abstract::Zileuton, an inhibitor of 5-lipooxygenase, the initial enzyme in the leukotriene pathway, was marketed as a new treatment for asthma. This drug has been associated with liver toxicity, which has limited its clinical usefulness. We provide evidence here that the liver toxicity likely involves a sequence of biotransform...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0341409

    authors: Joshi EM,Heasley BH,Chordia MD,Macdonald TL

    更新日期:2004-02-01 00:00:00

  • Quantitative Evaluation of Reactivity and Toxicity of Acyl Glucuronides by [35S]Cysteine Trapping.

    abstract::Acyl glucuronides (AGs) are reactive metabolites of carboxylic acid-containing drugs, which are associated with idiosyncratic toxicity (IDT) such as anaphylaxis, drug-induced liver injury, and so on. In this study, we developed a new in vitro approach for the quantitative assessment of the reactivity of AGs and their ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.9b00111

    authors: Harada H,Toyoda Y,Abe Y,Endo T,Takeda H

    更新日期:2019-10-21 00:00:00

  • Covalent modification at Cys151 dissociates the electrophile sensor Keap1 from the ubiquitin ligase CUL3.

    abstract::The regulation of cellular stress responses to electrophiles and oxidants is mediated by the transcription factor NF-E2-related factor 2 (Nrf2), which, in turn, is regulated by CUL-E3 (CUL3) ligase-mediated ubiquitylation. The Kelch-like ECH-associated protein 1 (Keap1) serves as an adapter between CUL3 and Nrf2. We u...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700302s

    authors: Rachakonda G,Xiong Y,Sekhar KR,Stamer SL,Liebler DC,Freeman ML

    更新日期:2008-03-01 00:00:00

  • Chemical and glutathione conjugation-related degradation of fotemustine: formation and characterization of a glutathione conjugate of diethyl (1-isocyanatoethyl)phosphonate, a reactive metabolite of fotemustine.

    abstract::Fotemustine is a chemotherapeutic drug for the treatment of melanoma. In this study, we investigated the metabolic and chemical stability of fotemustine with 31P-NMR and FAB-MS. In the absence of GSH, 95% of fotemustine decomposed rapidly into a reactive diethyl ethylphosphonate (DEP) isocyanate, both in rat liver S9 ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00039a016

    authors: Brakenhoff JP,Commandeur JN,de Kanter FJ,van Baar BL,Luijten WC,Vermeulen NP

    更新日期:1994-05-01 00:00:00

  • Inhibition of the alpha-ketoglutarate dehydrogenase and pyruvate dehydrogenase complexes by a putative aberrant metabolite of serotonin, tryptamine-4,5-dione.

    abstract::A transient energy impairment with resultant release and subsequent reuptake of 5-hydroxytryptamine (5-HT) and NMDA receptor activation with consequent cytoplasmic superoxide (O(2)(-)(*)), nitric oxide (NO(*)), and peroxynitrite (ONOO(-)) generation have all been implicated in a neurotoxic cascade which ultimately lea...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx020029b

    authors: Jiang XR,Dryhurst G

    更新日期:2002-10-01 00:00:00

  • 42,43,44,45,46,47,55-Heptanor-41-oxohomoyessotoxin, a new biotoxin from mussels of the northern Adriatic sea.

    abstract::The diarrhetic shellfish toxin composition in the digestive glands of mussels from the northern Adriatic sea was investigated. Along with known yessotoxins, identified by comparison of their chromatographic and spectral properties with those reported in the literature, we isolated a new analogue of yessotoxin, 42,43,4...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx000259v

    authors: Ciminiello P,Fattorusso E,Forino M,Poletti R

    更新日期:2001-05-01 00:00:00

  • (5'S)- and (5'R)-5',8-cyclo-2'-deoxyguanosine: mechanistic insights on the 2'-deoxyguanosin-5'-yl radical cyclization.

    abstract::The two diastereomeric forms (5'S) and (5'R) of 5',8-cyclo-2'-deoxyguanosine have been synthesized and fully characterized. They have been used as references for the investigation of gamma-irradiation of 2'-deoxyguanosine and photolysis of 8-bromo-2'-deoxyguanosine in aqueous solutions. The observed (5'R)/(5'S) ratio ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700282x

    authors: Chatgilialoglu C,Bazzanini R,Jimenez LB,Miranda MA

    更新日期:2007-12-01 00:00:00

  • Biochemical investigations into the mutagenic potential of 8-oxo-2'-deoxyguanosine using nucleotide analogues.

    abstract::8-Oxo-2'-deoxyguanosine (OdG) is an abundant DNA lesion produced during oxidative damage to DNA. It can form relatively stable base pairs with both dC and dA that mimic natural dG:dC and dT:dA base pairs, respectively. Thus, when in the template strand, OdG can direct the insertion of either dCTP or dATP during replic...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300365g

    authors: Hamm ML,Crowley KA,Ghio M,Lindell MA,McFadden EJ,Silberg JS,Weaver AM

    更新日期:2012-11-19 00:00:00

  • Protein binding and metabolism influence the relative skin sensitization potential of cinnamic compounds.

    abstract::Skin protein modification (haptenation) is thought to be a key step in the manifestation of sensitization to low molecular mass chemicals (<500 g/mol). For sensitizing chemicals that are not protein reactive, it is hypothesised that metabolic activation can convert such chemicals into protein reactive toxins within th...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0341456

    authors: Elahi EN,Wright Z,Hinselwood D,Hotchkiss SA,Basketter DA,Pease CK

    更新日期:2004-03-01 00:00:00

  • Increased levels of inosine in a mouse model of inflammation.

    abstract::One possible mechanism linking inflammation with cancer involves the generation of reactive oxygen, nitrogen, and halogen species by activated macrophages and neutrophils infiltrating sites of infection or tissue damage, with these chemical mediators causing damage that ultimately leads to cell death and mutation. To ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300473n

    authors: Prestwich EG,Mangerich A,Pang B,McFaline JL,Lonkar P,Sullivan MR,Trudel LJ,Taghizedeh K,Dedon PC

    更新日期:2013-04-15 00:00:00

  • The detection and identification of 42,43,44,45,46,47,55-heptanor-41-oxoyessotoxin, a new marine toxin from adriatic shellfish, by liquid chromatography-mass spectrometry.

    abstract::The diarrhetic shellfish toxin composition in the digestive glands of mussels collected in June 2001 from the Northern Adriatic sea was investigated by high-performance liquid chromatography coupled with electrospray ion trap mass spectrometry. Along with known yessotoxins (1, 3-6), identified by comparison of their r...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx025527z

    authors: Ciminiello P,Dell'Aversano C,Fattorusso E,Forino M,Magno S,Poletti R

    更新日期:2002-07-01 00:00:00

  • Metabolism of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline in human hepatocytes: 2-amino-3-methylimidazo[4,5-f]quinoxaline-8-carboxylic acid is a major detoxification pathway catalyzed by cytochrome P450 1A2.

    abstract::Metabolic pathways of the mutagen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) remain incompletely characterized in humans. In this study, the metabolism of MeIQx was investigated in primary human hepatocytes. Six metabolites were characterized by UV and mass spectroscopy. Novel metabolites were additionally ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx000176e

    authors: Langouët S,Welti DH,Kerriguy N,Fay LB,Huynh-Ba T,Markovic J,Guengerich FP,Guillouzo A,Turesky RJ

    更新日期:2001-02-01 00:00:00

  • No role of homologous recombination in dealing with β-lapachone cytotoxicity in yeast.

    abstract::β-Lapachone (β-lap) is a promising antitumoral agent. DNA base oxidation and alkylation are among the expected damages by β-lap. Herein, we have explored the role that the homologous recombination pathway (HR), a critical DNA repair process in Saccharomyces cerevisiae, has in the cytotoxic profile of β-lap. We have fu...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx2004618

    authors: Quevedo O,García-Luis J,Lorenzo-Castrillejo I,Machín F

    更新日期:2011-12-19 00:00:00

  • Molecular cytotoxicity mechanisms of allyl alcohol (acrolein) in budding yeast.

    abstract::Allyl alcohol (AA) is one of the environmental pollutants used as a herbicide and industrial chemical. AA undergoes enzymatic oxidation in vivo to form Acrolein (Acr), a highly reactive and ubiquitous environmental toxicant. The exposure to AA/Acr has detrimental effects on cells and is highly fatal. In corroboration ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.5b00071

    authors: Golla U,Bandi G,Tomar RS

    更新日期:2015-06-15 00:00:00

  • Interaction of Cd2+ with Zn finger 3 of transcription factor IIIA: structures and binding to cognate DNA.

    abstract::Finger 3 of transcription factor IIIA of Xenopus laevis was synthesized and constituted with Zn(2+) or Cd(2+). The C-block element of the internal control region of the promoter of the 5S rRNA gene binds to the Zn-F3 and Cd-F3 with dissociation constants of 2.6 x 10(-5) and 1.5 x 10(-4) M, respectively. According to N...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx030057+

    authors: Krepkiy D,Försterling FH,Petering DH

    更新日期:2004-07-01 00:00:00

  • Genotoxicity-related chemistry of human metabolites of benzo[ghi]perylene (B[ghi]P) investigated using electro-optical arrays and DNA/microsome biocolloid reactors with LC-MS/MS.

    abstract::There is limited and sometimes contradictory information about the genotoxicity of the polycyclic aromatic hydrocarbon benzo[ghi]perylene (B[ghi]P). Using recently developed metabolic toxicity screening arrays and a biocolloid reactor-LC-MS/MS approach, both featuring films of DNA and human metabolic enzymes, we demon...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx400147c

    authors: Pan S,Li D,Zhao L,Schenkman JB,Rusling JF

    更新日期:2013-08-19 00:00:00

  • Neurotoxic potential and cellular uptake of T-2 toxin in human astrocytes in primary culture.

    abstract::The trichothecene mycotoxin T-2 toxin, which is produced by fungi of the Fusarium species, is a worldwide occurring contaminant of cereal based food and feed. The cytotoxic properties of T-2 toxin are already well described with apoptosis being a major mechanism of action in various cell lines as well as in primary ce...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx3004664

    authors: Weidner M,Lenczyk M,Schwerdt G,Gekle M,Humpf HU

    更新日期:2013-03-18 00:00:00

  • Hydroxywarfarin metabolites potently inhibit CYP2C9 metabolism of S-warfarin.

    abstract::Coumadin (R/S-warfarin) anticoagulant therapy poses a risk to over 50 million Americans, in part due to interpersonal variation in drug metabolism. Consequently, it is important to understand how metabolic capacity is influenced among patients. Cytochrome P450s (P450 or CYP for a specific isoform) catalyze the first m...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx1000283

    authors: Jones DR,Kim SY,Guderyon M,Yun CH,Moran JH,Miller GP

    更新日期:2010-05-17 00:00:00

  • Use of electrochemical oxidation and model peptides to study nucleophilic biological targets of reactive metabolites: the case of rimonabant.

    abstract::Electrochemical oxidation of drug molecules is a useful tool to generate several different types of metabolites. In the present study we developed a model system involving electrochemical oxidation followed by characterization of the oxidation products and their propensity to modify peptides. The CB1 antagonist rimona...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500255r

    authors: Thorsell A,Isin EM,Jurva U

    更新日期:2014-10-20 00:00:00

  • Potentialities and pitfalls accompanying chemico-pharmacological strategies against endogenous electrophiles and carbonyl stress.

    abstract::The use of powerful analytical technologies to detect endogenous carbonyls formed as byproducts of oxidative cell injury has revealed that these species contribute to many human diseases. As electrophiles, they are attacked by reactive centers in cell macromolecules to form adducts, the levels of which serve as useful...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700399q

    authors: Burcham PC

    更新日期:2008-04-01 00:00:00

  • Novel resveratrol-based substrates for human hepatic, renal, and intestinal UDP-glucuronosyltransferases.

    abstract::Trans-Resveratrol (tRes) has been shown to have powerful antioxidant, anti-inflammatory, anticarcinogenic, and antiaging properties; however, its use as a therapeutic agent is limited by its rapid metabolism into its conjugated forms by UDP-glucuronosyltransferases (UGTs). The aim of the current study was to test the ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx400408x

    authors: Greer AK,Madadi NR,Bratton SM,Eddy SD,Mazerska Z,Hendrickson HP,Crooks PA,Radominska-Pandya A

    更新日期:2014-04-21 00:00:00

  • Drug metabolite-specific lymphocyte responses in sulfamethoxazole allergic patients with cystic fibrosis.

    abstract::Sulfamethoxazole (SMX) is an important antibiotic in the management of patients with cystic fibrosis, but allergic reactions may develop thus restricting therapy. The aim of this study was to utilize drug (metabolite) antigens to diagnose SMX-mediated allergic reactions in patients with cystic fibrosis. Lymphocytes fr...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx100151v

    authors: Lavergne SN,Whitaker P,Peckham D,Conway S,Park BK,Naisbitt DJ

    更新日期:2010-06-21 00:00:00

  • Base sequence-dependent bends in site-specific benzo[a]pyrene diol epoxide-modified oligonucleotide duplexes.

    abstract::The site specifically modified oligonucleotides 5'-d(TCCTCCTG1G2CCTCTC) (I) and 5'-d(CTATG1G2G3TATC) (II) were synthesized with single modified guanine residues at positions G1, G2, or G3, derived from the covalent binding reaction of 7R,8S-dihydroxy-9S,10R-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene ((+)-anti-BPDE) with ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx9501086

    authors: Liu T,Xu J,Tsao H,Li B,Xu R,Yang C,Amin S,Moriya M,Geacintov NE

    更新日期:1996-01-01 00:00:00

  • Enzyme-linked immunosorbent assay for the specific detection of the mercapturic acid metabolites of naphthalene.

    abstract::The measurement of metabolites constitutes a useful tool for detection of exposure and in pharmacokinetic studies. Epoxidation with subsequent glutathione conjugation and mercapturic acid formation is an important deactivation pathway for naphthalene, a toxin which presumably causes lung disease. The mercapturic acid ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00033a006

    authors: Marco MP,Nasiri M,Kurth MJ,Hammock BD

    更新日期:1993-05-01 00:00:00

  • Identification and quantification of DNA adducts in the oral tissues of mice treated with the environmental carcinogen dibenzo[a,l]pyrene by HPLC-MS/MS.

    abstract::Tobacco smoking is one of the leading causes for oral cancer. Dibenzo[a,l]pyrene (DB[a,l]P), an environmental pollutant and a tobacco smoke constituent, is the most carcinogenic polycyclic aromatic hydrocarbon (PAH) tested to date in several animal models (target organs: skin, lung, ovary, and mammary tissues). We hav...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx200188j

    authors: Zhang SM,Chen KM,Aliaga C,Sun YW,Lin JM,Sharma AK,Amin S,El-Bayoumy K

    更新日期:2011-08-15 00:00:00

  • Determination of the Cd/S cluster stoichiometry in Fucus vesiculosus metallothionein.

    abstract::The seaweed Fucus vesiculosus is unusual when compared with other algal species, in that it can survive in toxic-metal-contaminated aquatic environments. The metallothionein gene has been identified in F. vesiculosus by Kille and co-workers (Morris, C. A., Nicolaus, B., Sampson, V., Harwood, J. L., and Kille, P. (1999...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx050206j

    authors: Merrifield ME,Chaseley J,Kille P,Stillman MJ

    更新日期:2006-03-01 00:00:00

  • Inhibition of topoisomerase I function by nitidine and fagaronine.

    abstract::The benzophenanthridine alkaloids nitidine and fagaronine were characterized as inhibitors of topoisomerase I function. In common with the antitumor agent camptothecin, both nitidine and fagaronine stabilized the covalent binary complex formed between calf thymus topoisomerase I and DNA. The effects of these compounds...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00036a010

    authors: Wang LK,Johnson RK,Hecht SM

    更新日期:1993-11-01 00:00:00

  • Mechanism of formation of ethenoguanine adducts from 2-haloacetaldehydes: 13C-labeling patterns with 2-bromoacetaldehyde.

    abstract::The mechanism of formation of etheno (epsilon) adducts of nucleic acid bases from 2-haloacetaldehydes is generally assumed to occur via initial Schiff base formation resulting from reaction of the aldehyde with an exocyclic amine. We recently revised the 1H NMR assignments of the epsilon protons of 1,N2-epsilon-Guo (G...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00038a014

    authors: Guengerich FP,Persmark M

    更新日期:1994-03-01 00:00:00