Literature DB >> 11275477

Identification and quantification of 8,5'-cyclo-2'-deoxy-adenosine in DNA by liquid chromatography/ mass spectrometry.

M Dizdaroglu1, P Jaruga, H Rodriguez.   

Abstract

Recent studies suggested that 8,5'-cyclo-2'-deoxyadenosine may play a role in diseases with defective nucleotide-excision repair. This compound is one of the major lesions, which is formed in DNA by hydroxyl radical attack on the sugar moiety of 2'-deoxyadenosine. It is likely to be repaired by nucleotide-excision repair rather than by base-excision repair because of a covalent bond between the sugar and base moieties. We studied the measurement of 8,5'-cyclo-2'-deoxyadenosine in DNA by liquid chromatography/isotope-dilution mass spectrometry. A methodology was developed for the analysis of 8,5'-cyclo-2'-deoxyadenosine by liquid chromatography in DNA hydrolyzed to nucleosides by a combination of four enzymes, i.e., DNase I, phosphodiesterases I and II, and alkaline phosphatase. Detection by mass spectrometry was performed using atmospheric pressure ionization-electrospray process in the positive ionization mode. Results showed that liquid chromatography/isotope-dilution mass spectrometry is well suited for identification and quantification of 8,5'-cyclo-2'-deoxyadenosine in DNA. Both (5'R)- and (5'S)-diastereomers of 8,5'-cyclo-2'-deoxyadenosine were detected. The level of sensitivity of liquid chromatography/mass spectrometry with selected-ion monitoring amounted to 2 fmol of this compound on the column. The yield of 8,5'-cyclo-2'-deoxyadenosine was measured in DNA in aqueous solution exposed to ionizing radiation at doses from 2.5 to 80 Gray. Gas chromatography/mass spectrometry was also used to measure this compound in DNA. Both techniques yielded similar results. The yield of 8,5'-cyclo-2'-deoxyadenosine was comparable to the yields of some of the other major modified bases in DNA, which were measured using gas chromatography/mass spectrometry. The measurement of 8,5'-cyclo-2'-deoxyadenosine by liquid chromatography/mass spectrometry may contribute to the understanding of its biological properties and its role in diseases with defective nucleotide-excision repair.

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Year:  2001        PMID: 11275477     DOI: 10.1016/s0891-5849(01)00464-6

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  22 in total

Review 1.  Biologically relevant oxidants and terminology, classification and nomenclature of oxidatively generated damage to nucleobases and 2-deoxyribose in nucleic acids.

Authors:  Jean Cadet; Steffen Loft; Ryszard Olinski; Mark D Evans; Karol Bialkowski; J Richard Wagner; Peter C Dedon; Peter Møller; Marc M Greenberg; Marcus S Cooke
Journal:  Free Radic Res       Date:  2012-02-22

2.  Top-down mass spectrometry for sequencing of larger (up to 61 nt) RNA by CAD and EDD.

Authors:  Monika Taucher; Kathrin Breuker
Journal:  J Am Soc Mass Spectrom       Date:  2010-03-09       Impact factor: 3.109

3.  Quantification of DNA damage products resulting from deamination, oxidation and reaction with products of lipid peroxidation by liquid chromatography isotope dilution tandem mass spectrometry.

Authors:  Koli Taghizadeh; Jose L McFaline; Bo Pang; Matthew Sullivan; Min Dong; Elaine Plummer; Peter C Dedon
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

Review 4.  An overview of chemical processes that damage cellular DNA: spontaneous hydrolysis, alkylation, and reactions with radicals.

Authors:  Kent S Gates
Journal:  Chem Res Toxicol       Date:  2009-11       Impact factor: 3.739

Review 5.  Formation and repair of oxidatively generated damage in cellular DNA.

Authors:  Jean Cadet; Kelvin J A Davies; Marisa Hg Medeiros; Paolo Di Mascio; J Richard Wagner
Journal:  Free Radic Biol Med       Date:  2017-01-02       Impact factor: 7.376

6.  Structure and stability of duplex DNA containing (5'S)-5',8-cyclo-2'-deoxyadenosine: an oxidatively generated lesion repaired by NER.

Authors:  Tatiana Zaliznyak; Mark Lukin; Carlos de los Santos
Journal:  Chem Res Toxicol       Date:  2012-09-11       Impact factor: 3.739

7.  Stability of N-glycosidic bond of (5'S)-8,5'-cyclo-2'-deoxyguanosine.

Authors:  Rajat S Das; Milinda Samaraweera; Martha Morton; José A Gascón; Ashis K Basu
Journal:  Chem Res Toxicol       Date:  2012-10-15       Impact factor: 3.739

8.  Synthesis of [1,3, NH2-(15)N3] (5'S)-8,5'-cyclo-2'-deoxyguanosine.

Authors:  Chanchal K Malik; Rajat S Das; Ashis K Basu
Journal:  J Labelled Comp Radiopharm       Date:  2013-05-23       Impact factor: 1.921

9.  Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.

Authors:  Güldal Kirkali; Nadja C de Souza-Pinto; Pawel Jaruga; Vilhelm A Bohr; Miral Dizdaroglu
Journal:  DNA Repair (Amst)       Date:  2008-11-18

10.  Repair efficiency of (5'S)-8,5'-cyclo-2'-deoxyguanosine and (5'S)-8,5'-cyclo-2'-deoxyadenosine depends on the complementary base.

Authors:  Paritosh Pande; Rajat S Das; Clayton Sheppard; Yoke W Kow; Ashis K Basu
Journal:  DNA Repair (Amst)       Date:  2012-10-10
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