Literature DB >> 7578905

Conformational studies of the (+)-trans, (-)-trans, (+)-cis, and (-)-cis adducts of anti-benzo[a]pyrene diolepoxide to N2-dG in duplex oligonucleotides using polyacrylamide gel electrophoresis and low-temperature fluorescence spectroscopy.

M Suh1, F Ariese, G J Small, R Jankowiak, T M Liu, N E Geacintov.   

Abstract

Using polyacrylamide gel electrophoresis (PAGE) and low-temperature, laser-induced fluorescence line narrowing (FLN) and non-line narrowing (NLN) spectroscopic methods, the conformational characteristics of stereochemically defined and site-specific adducts derived from the binding of 7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene (anti-BPDE, a metabolite of the environmental carcinogen benzo[a]pyrene), to DNA were studied. The focus of these studies was on the four stereochemically distinct anti-BPDE modified duplexes 5'-d(CCATCGCTACC).(GGTAGCGATGG), where G denotes the lesion site derived from trans or cis addition of the exocyclic amino group of guanine to the C10 position of either (+) or (-)-anti-BPDE. PAGE experiments under non-denaturing conditions showed that the (+)-trans adduct causes a significantly greater retardation in the electrophoretic mobility than the other three adducts, probably the result of important adduct-induced distortions of the duplex structure. Low-temperature fluorescence studies in frozen aqueous buffer matrices showed that the (+)-trans adduct adopts primarily an external conformation with only minor interactions with the helix, but a smaller fraction (approximately 25%) appears to exists in a partially base-stacked conformation. The (-)-trans adduct exists almost exclusively (approximately 97%) in an external conformation. Both cis adducts were found to be intercalated; strong electron-phonon coupling observed in their FLN spectra provided additional evidence for significant pi-pi stacking interactions between the pyrenyl residues and the bases. FLN spectroscopy is shown to be suitable for distinguishing between trans and cis adducts, but lesions with either (+)- or (-)-trans, or (+)- or (-)-cis stereochemical characteristics showed very similar vibrational patterns.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7578905     DOI: 10.1016/0301-4622(95)00055-3

Source DB:  PubMed          Journal:  Biophys Chem        ISSN: 0301-4622            Impact factor:   2.352


  3 in total

1.  Distant neighbor base sequence context effects in human nucleotide excision repair of a benzo[a]pyrene-derived DNA lesion.

Authors:  Yuqin Cai; Konstantin Kropachev; Rong Xu; Yijin Tang; Marina Kolbanovskii; Alexander Kolbanovskii; Shantu Amin; Dinshaw J Patel; Suse Broyde; Nicholas E Geacintov
Journal:  J Mol Biol       Date:  2010-04-22       Impact factor: 5.469

2.  Influence of C-5 substituted cytosine and related nucleoside analogs on the formation of benzo[a]pyrene diol epoxide-dG adducts at CG base pairs of DNA.

Authors:  Rebecca Guza; Delshanee Kotandeniya; Kristopher Murphy; Thakshila Dissanayake; Chen Lin; George Madalin Giambasu; Rahul R Lad; Filip Wojciechowski; Shantu Amin; Shana J Sturla; Robert H E Hudson; Darrin M York; Ryszard Jankowiak; Roger Jones; Natalia Y Tretyakova
Journal:  Nucleic Acids Res       Date:  2011-01-17       Impact factor: 16.971

3.  Unusual sequence effects on nucleotide excision repair of arylamine lesions: DNA bending/distortion as a primary recognition factor.

Authors:  Vipin Jain; Benjamin Hilton; Bin Lin; Satyakam Patnaik; Fengting Liang; Eva Darian; Yue Zou; Alexander D Mackerell; Bongsup P Cho
Journal:  Nucleic Acids Res       Date:  2012-11-23       Impact factor: 16.971

  3 in total

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