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GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin.

GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Research Abstract Details 

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  • GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Abstract Text:

    bingzi chenBingzi Chen,xinfeng zhouXinfeng Zhou,koli taghizadehKoli Taghizadeh,jingyang chenJingyang Chen,joanne stubbeJoanne Stubbe,peter c dedonPeter C Dedon,bingzi chenBingzi Chen,xinfeng zhouXinfeng Zhou,koli taghizadehKoli Taghizadeh,jingyang chenJingyang Chen,joanne stubbeJoAnne Stubbe,peter c dedonPeter C Dedon,bingzi chenBingzi Chen,xinfeng zhouXinfeng Zhou,koli taghizadehKoli Taghizadeh,jingyang chenJingyang Chen,joanne stubbeJoAnne Stubbe,peter c dedonPeter C Dedon,bingzi chenBingzi Chen,xinfeng zhouXinfeng Zhou,koli taghizadehKoli Taghizadeh,jingyang chenJingyang Chen,joanne stubbeJoAnne Stubbe,peter c dedonPeter C Dedon,

    DNA oxidation plays a substantive role in the pathophysiology of human diseases, such as cancer. While the chemistry of nucleobase lesions has dominated studies of DNA damage, there is growing evidence that the oxidation of 2-deoxyribose in DNA plays a critical role in the genetic toxicology of oxidative stress. As part of an effort to define the spectrum of 2-deoxyribose oxidation products arising in vitro and in vivo, we now describe methods for quantifying products arising from 4' oxidation of 2-deoxyribose in DNA. The chemistry of 4' oxidation partitions between either of two pathways to form either a 2-deoxypentos-4-ulose abasic site (oxAB) or a strand break comprised of a 3'-phosphoglycolate (3PG) residue and a 5'-phosphate, with the release of either malondialdehyde and free base or a base propenal. Highly sensitive gas chromatography/mass spectrometry (GC/MS) methods were developed to quantify both lesions. The abasic site was converted to a 3'-phosphoro-3-pyridazinylmethylate derivative by treatment of the damaged DNA with hydrazine, which was released from DNA as 3-hydroxymethylpyridazine (HMP) by enzymatic hydrolysis. Similarly, 3PG was released as 2-phosphoglycolic acid (PG) by enzymatic hydrolysis. Following HPLC prepurification, both PG and HMP were silylated and quantified by GC/MS, with limits of detection of 100 and 200 fmol and sensitivities of 2 and 4 lesions per 10 (6) nucleotides (nt) in 250 microg of DNA, respectively. Following validation of the methods with oligodeoxynucleotides containing the two lesions, the methods were applied to DNA damage produced by bleomycin and gamma radiation. As expected for an agent known to produce only 4' oxidation of DNA, the quantities of 3PG and oxAB accounted for all 2-deoxyribose oxidation events, as indicated by slopes of 0.8 and 0.3, respectively, in plots of the lesion frequency against total 2-deoxyribose oxidation events, with the latter determined by a plasmid-nicking assay. 3PG residues and oxAB were produced at the rate of 32 and 12 lesions per 10 (6) nt per microM, respectively. For gamma radiation, on the other hand, 4' oxidation was found to comprise only 13% of 2-deoxyribose oxidation chemistry, with 3% oxAB (4 per 10 (6) nt per Gy) and 10% 3PG (13 per 10 (6) nt per Gy).

    GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Publishing Authors By Initials

    b chenB Chen,x zhouX Zhou,k taghizadehK Taghizadeh,j chenJ Chen,j stubbeJ Stubbe,pc dedonPC Dedon,b chenB Chen,x zhouX Zhou,k taghizadehK Taghizadeh,j chenJ Chen,j stubbeJ Stubbe,pc dedonPC Dedon,b chenB Chen,x zhouX Zhou,k taghizadehK Taghizadeh,j chenJ Chen,j stubbeJ Stubbe,pc dedonPC Dedon,b chenB Chen,x zhouX Zhou,k taghizadehK Taghizadeh,j chenJ Chen,j stubbeJ Stubbe,pc dedonPC Dedon,

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    GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Chemical research in toxicology

    VOLUME: 20

    Page Numbers: 1701-8

    Journal Abbreviation: Chem. Res. Toxicol.

    ISSN: 0893-228X

    DAY: 19

    MONTH: 10

    YEAR: 2007

    GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Information

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    LANGUAGE: eng

    NlmUniqueID: 8807448

    GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin. Information

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    AFFILIATION: pcdedon@mit.edu.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Chem Res Toxicol

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    GC/MS Methods To Quantify the 2-Deoxypentos-4-ulose and 3'-Phosphoglycolate Pathways of 4' Oxidation of 2-Deoxyribose in DNA: Application to DNA Damage Produced by gamma Radiation and Bleomycin Related Publications

     

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