Literature DB >> 19937959

Absolute configurations of DNA lesions determined by comparisons of experimental ECD and ORD spectra with DFT calculations.

Shuang Ding1, Alexander Kolbanovskiy, Alexander Durandin, Conor Crean, Vladimir Shafirovich, Suse Broyde, Nicholas E Geacintov.   

Abstract

The usefulness of modern density functional theory (DFT) methods is considered for establishing the absolute configurations of DNA lesions by comparisons of computed and experimentally measured optical rotatory dispersion (ORD) and electronic circular dichroism (<span class="Disease">ECD) spectra. Two rigid, structurally different DNA lesions (two spiroiminodihydantoin stereoisomers and four equine estrogen 4-hydoxyequilenin-DNA stereoisomeric adducts) have been investigated. In all cases, the signs and shapes of the computed ORD spectra reproduced the experimentally measured ORD spectra, although the magnitudes of the computed and experimental ORD values do not coincide exactly. The computed ECD spectra also reproduced the shapes of the experimental ECD spectra rather well, but are blue-shifted by 10-20 nm. Since the assignments of the absolute configurations of the DNA lesions studied based on computed and experimental ORD and ECD spectra are fully consistent with one another, the computational DFT method shows significant promise for determining the absolute configurations of DNA lesions. Establishing the stereochemistry of DNA lesions is highly useful for understanding their biological impact, especially when sufficient amounts of material are not available for other methods of structural characterization. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19937959      PMCID: PMC4033673          DOI: 10.1002/chir.20804

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  85 in total

1.  Determining absolute configuration in flexible molecules: a case study.

Authors:  K M Specht; J Nam; D M Ho; N Berova; R K Kondru; D N Beratan; P Wipf; R A Pascal; D Kahne
Journal:  J Am Chem Soc       Date:  2001-09-19       Impact factor: 15.419

2.  Detection of estrogen DNA-adducts in human breast tumor tissue and healthy tissue by combined nano LC-nano ES tandem mass spectrometry.

Authors:  J Embrechts; F Lemière; W Van Dongen; E L Esmans; P Buytaert; E Van Marck; M Kockx; A Makar
Journal:  J Am Soc Mass Spectrom       Date:  2003-05       Impact factor: 3.109

3.  Determination of absolute configuration using ab initio calculation of optical rotation.

Authors:  P J Stephens; F J Devlin; J R Cheeseman; M J Frisch; O Bortolini; P Besse
Journal:  Chirality       Date:  2003       Impact factor: 2.437

Review 4.  Nature and nurture - lessons from chemical carcinogenesis.

Authors:  Andreas Luch
Journal:  Nat Rev Cancer       Date:  2005-02       Impact factor: 60.716

5.  Base selectivity and effects of sequence and DNA secondary structure on the formation of covalent adducts derived from the equine estrogen metabolite 4-hydroxyequilenin.

Authors:  Alexander Kolbanovskiy; Vladimir Kuzmin; Anant Shastry; Marina Kolbanovskaya; Dandan Chen; Minsun Chang; Judith L Bolton; Nicholas E Geacintov
Journal:  Chem Res Toxicol       Date:  2005-11       Impact factor: 3.739

Review 6.  Role of quinoids in estrogen carcinogenesis.

Authors:  J L Bolton; E Pisha; F Zhang; S Qiu
Journal:  Chem Res Toxicol       Date:  1998-10       Impact factor: 3.739

7.  Spiroiminodihydantoin is a major product in the photooxidation of 2'-deoxyguanosine by the triplet states and oxyl radicals generated from hydroxyacetophenone photolysis and dioxetane thermolysis.

Authors:  Waldemar Adam; Markus A Arnold; Matthias Grüne; Werner M Nau; Uwe Pischel; Chantu R Saha-Möller
Journal:  Org Lett       Date:  2002-02-21       Impact factor: 6.005

8.  Impact of the oxidized guanine lesion spiroiminodihydantoin on the conformation and thermodynamic stability of a 15-mer DNA duplex.

Authors:  Fadzai Chinyengetere; Elizabeth R Jamieson
Journal:  Biochemistry       Date:  2008-02-26       Impact factor: 3.162

9.  Translesional synthesis on a DNA template containing a single stereoisomer of dG-(+)- or dG-(-)-anti-BPDE (7,8-dihydroxy-anti-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene).

Authors:  S Shibutani; L A Margulis; N E Geacintov; A P Grollman
Journal:  Biochemistry       Date:  1993-07-27       Impact factor: 3.162

10.  The decrease in breast-cancer incidence in 2003 in the United States.

Authors:  Peter M Ravdin; Kathleen A Cronin; Nadia Howlader; Christine D Berg; Rowan T Chlebowski; Eric J Feuer; Brenda K Edwards; Donald A Berry
Journal:  N Engl J Med       Date:  2007-04-19       Impact factor: 91.245

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  4 in total

1.  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

2.  Thermodynamic profiles and nuclear magnetic resonance studies of oligonucleotide duplexes containing single diastereomeric spiroiminodihydantoin lesions.

Authors:  Irine Khutsishvili; Na Zhang; Luis A Marky; Conor Crean; Dinshaw J Patel; Nicholas E Geacintov; Vladimir Shafirovich
Journal:  Biochemistry       Date:  2013-02-13       Impact factor: 3.162

3.  Assignment of Vibrational Circular Dichroism Cross-Referenced Electronic Circular Dichroism Spectra of Flexible Foldamer Building Blocks: Towards Assigning Pure Chiroptical Properties of Foldamers.

Authors:  Viktor Farkas; Adrienn Nagy; Dóra K Menyhárd; András Perczel
Journal:  Chemistry       Date:  2019-10-23       Impact factor: 5.236

Review 4.  Understanding DNA under oxidative stress and sensitization: the role of molecular modeling.

Authors:  Elise Dumont; Antonio Monari
Journal:  Front Chem       Date:  2015-07-14       Impact factor: 5.221

  4 in total

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