Literature DB >> 10747804

Strand cleavage of supercoiled DNA by water-soluble peroxyl radicals. The overlooked importance of peroxyl radical charge.

T Paul1, M J Young, I E Hill, K U Ingold.   

Abstract

It is well established that the peroxyl radicals formed during the thermal decomposition of 2,2'-azobis(amidinopropane), ABAP, in oxygenated water can cleave double-stranded DNA, from which fact it has been concluded that peroxyl radicals, as a general class, can induce DNA strand scission. However, the ABAP-derived radicals are positively charged, and DNA is a negatively charged polyanion. Moreover, the relatively small and, therefore, free to diffuse peroxyl radicals likely to be formed in vivo will generally be negatively charged or neutral. Plasmid supercoiled DNA [pBR 322, 4361 base pairs (bp)] was reacted with known, equal fluxes of two positively charged peroxyl radicals, a negatively charged peroxyl radical, and a neutral peroxyl radical. The two positively charged peroxyl radicals degraded >/=80% of the supercoiled pBR 322 at a flux of 4 radicals/bp, but the negatively charged and neutral peroxyl radicals had no significant effect even at a flux as high as 24 radicals/bp. The same lack of effect on the DNA was also observed with high fluxes of superoxide/hydroperoxyl radicals. Similar results were obtained with another supercoiled DNA, pUC 19, except that pUC 19 is somewhat more sensitive to strand scission by positively charged peroxyl radicals than pBR 322. We conclude that most of the peroxyl radicals likely to be formed in vivo have little or no ability to induce DNA strand scission and that the potential role of electrostatics in radical/DNA reactions should always be considered.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10747804     DOI: 10.1021/bi991463o

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  5 in total

1.  Structure-dependent reactivity of oxyfunctionalized acetophenones in the photooxidation of DNA: base oxidation and strand breaks through photolytic radical formation (spin trapping, EPR spectroscopy, transient kinetics) versus photosensitization (electron transfer, hydrogen-atom abstraction).

Authors:  W Adam; M A Arnold; W M Nau; U Pischel; C R Saha-Möller
Journal:  Nucleic Acids Res       Date:  2001-12-15       Impact factor: 16.971

2.  Direct real-time molecular scale visualisation of the degradation of condensed DNA complexes exposed to DNase I.

Authors:  Hosam G Abdelhady; Stephanie Allen; Martyn C Davies; Clive J Roberts; Saul J B Tendler; Philip M Williams
Journal:  Nucleic Acids Res       Date:  2003-07-15       Impact factor: 16.971

3.  Oxidation of 8-oxo-7,8-dihydro-2'-deoxyguanosine by oxyl radicals produced by photolysis of azo compounds.

Authors:  Jie Shao; Nicholas E Geacintov; Vladimir Shafirovich
Journal:  Chem Res Toxicol       Date:  2010-05-17       Impact factor: 3.739

4.  Oxidative modification of guanine bases initiated by oxyl radicals derived from photolysis of azo compounds.

Authors:  Jie Shao; Nicholas E Geacintov; Vladimir Shafirovich
Journal:  J Phys Chem B       Date:  2010-05-20       Impact factor: 2.991

5.  DNA sequence context as a determinant of the quantity and chemistry of guanine oxidation produced by hydroxyl radicals and one-electron oxidants.

Authors:  Yelena Margolin; Vladimir Shafirovich; Nicholas E Geacintov; Michael S DeMott; Peter C Dedon
Journal:  J Biol Chem       Date:  2008-10-23       Impact factor: 5.157

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.