Literature DB >> 16791886

Guanine oxidation: one- and two-electron reactions.

Geneviève Pratviel1, Bernard Meunier.   

Abstract

Guanine bases in DNA are the most sensitive to oxidation. A lot of effort has been devoted to the understanding of the chemical modifications of guanine under different oxidizing conditions, the final goal being to know which lesions in DNA can be expected in vivo and their biological consequences. This article analyses the mechanisms underlying guanine oxidation by the comparison between one- and two-electron transfer processes. The different oxidants used in vitro give complementary answers. This overview presents a choice of some key intermediates and the predictive description of G-oxidation products that can be generated from these intermediates depending on the reaction conditions.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16791886     DOI: 10.1002/chem.200600539

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  30 in total

1.  Comparison of Transition Metal-Mediated Oxidation Reactions of Guanine in Nucleoside and Single-Stranded Oligodeoxynucleotide Contexts.

Authors:  Pranjali Ghude; Mark A Schallenberger; Aaron M Fleming; James G Muller; Cynthia J Burrows
Journal:  Inorganica Chim Acta       Date:  2011-04-15       Impact factor: 2.545

2.  Biochemical identification of a hydroperoxide derivative of the free 8-oxo-7,8-dihydroguanine base.

Authors:  Gyorgy Hajas; Attila Bacsi; Leopoldo Aguilerra-Aguirre; Peter German; Zsolt Radak; Sanjiv Sur; Tapas K Hazra; Istvan Boldogh
Journal:  Free Radic Biol Med       Date:  2011-12-01       Impact factor: 7.376

Review 3.  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

4.  pH-Dependent Equilibrium between 5-Guanidinohydantoin and Iminoallantoin Affects Nucleotide Insertion Opposite the DNA Lesion.

Authors:  Judy Zhu; Aaron M Fleming; Anita M Orendt; Cynthia J Burrows
Journal:  J Org Chem       Date:  2015-11-24       Impact factor: 4.354

5.  A biochemical and biophysical model of G-quadruplex DNA recognition by positive coactivator of transcription 4.

Authors:  Wezley C Griffin; Jun Gao; Alicia K Byrd; Shubeena Chib; Kevin D Raney
Journal:  J Biol Chem       Date:  2017-04-17       Impact factor: 5.157

6.  G-quadruplex folds of the human telomere sequence alter the site reactivity and reaction pathway of guanine oxidation compared to duplex DNA.

Authors:  Aaron M Fleming; Cynthia J Burrows
Journal:  Chem Res Toxicol       Date:  2013-03-13       Impact factor: 3.739

7.  Biologically relevant oxidants cause bound proteins to readily oxidatively cross-link at Guanine.

Authors:  Morwena J Solivio; Dessalegn B Nemera; Larry Sallans; Edward J Merino
Journal:  Chem Res Toxicol       Date:  2012-02-06       Impact factor: 3.739

8.  Reconciliation of chemical, enzymatic, spectroscopic and computational data to assign the absolute configuration of the DNA base lesion spiroiminodihydantoin.

Authors:  Aaron M Fleming; Anita M Orendt; Yanan He; Judy Zhu; Rina K Dukor; Cynthia J Burrows
Journal:  J Am Chem Soc       Date:  2013-11-21       Impact factor: 15.419

9.  Iminohydantoin lesion induced in DNA by peracids and other epoxidizing oxidants.

Authors:  Wenjie Ye; R Sangaiah; Diana E Degen; Avram Gold; K Jayaraj; Karl M Koshlap; Gunnar Boysen; Jason Williams; Kenneth B Tomer; Viorel Mocanu; Nedyalka Dicheva; Carol E Parker; Roel M Schaaper; Louise M Ball
Journal:  J Am Chem Soc       Date:  2009-05-06       Impact factor: 15.419

10.  Structural context effects in the oxidation of 8-oxo-7,8-dihydro-2'-deoxyguanosine to hydantoin products: electrostatics, base stacking, and base pairing.

Authors:  Aaron M Fleming; James G Muller; Adrienne C Dlouhy; Cynthia J Burrows
Journal:  J Am Chem Soc       Date:  2012-08-29       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.