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PMID: 11087351 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

NMR evidence for syn-anti interconversion of a trans opened (10R)-dA adduct of benzo[a]pyrene (7S,8R)-diol (9R,10S)-epoxide in a DNA duplex.

Biochemistry ·Vol. 39 ·No. 46 ·2000-11-21 ·Pages 14040-53

Volk DE, Rice JS, Luxon BA, Yeh HJ, Liang C, Xie G, Sayer JM, Jerina DM, Gorenstein DG

Abstract

2D NMR has been used to examine the structure and dynamics of a 12-mer DNA duplex, d(T(1)A(2)G(3)T(4)C(5)A(6)A(7)G(8)G(9)G(10)C(11)A(12))-d(T(13)G(14)C( 15)C(16)C(17)T(18)T(19)G(20)A(21)C(22)T(23)A(24)), containing a 10R adduct at dA(7) that corresponds to trans addition of the N(6)-amino group of dA(7) to (-)-(7S,8R,9R,10S)-7,8-dihydroxy-9, 10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene [(-)-(S,R,R,S)-BP DE-2]. This DNA duplex contains the base sequence for the major dA mutational hot spot in the HPRT gene when Chinese hamster V79 cells are given low doses of the highly carcinogenic (+)-(R,S,S,R)-BP DE-2 enantiomer. NOE data indicate that the hydrocarbon is intercalated on the 5'-side of the modified base as has been seen previously for other oligonucleotides containing BP DE-2 (10R)-dA adducts. 2D chemical exchange-only experiments indicate dynamic behavior near the intercalation site especially at the 10R adducted dA, such that this base interconverts between the normal anti conformation and a less populated syn conformation. Ab initio molecular orbital chemical shift calculations of nucleotide and dinucleotide fragments in the syn and anti conformations support these conclusions. Although this DNA duplex containing a 10R dA adduct exhibits conformational flexibility as described, it is nevertheless more conformationally stable than the corresponding 10S adducted duplex corresponding to trans opening of the carcinogenic isomer (+)-(R,S,S, R)-BP DE-2, which was too dynamic to permit NMR structure determination. UV and imino proton NMR spectral observations indicated pronounced differences between these two diastereomeric 12-mer duplexes, consistent with conformational disorder at the adduct site and/or an equilibrium with a nonintercalated orientation of the hydrocarbon in the duplex containing the 10S adduct. The existence of conformational flexibility around adducts may be related to the occurrence of multiple mutagenic outcomes resulting from a single DE adduct.

MeSH Terms
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide/chemistry Chrysenes/chemistry Crystallography, X-Ray DNA Adducts/chemistry Deoxyadenosines/chemistry Intercalating Agents/chemistry Nuclear Magnetic Resonance, Biomolecular/methods Nucleic Acid Heteroduplexes/chemistry Oligonucleotides/chemistry Protein Conformation Protons Stereoisomerism Thermodynamics
Chemicals
Chrysenes DNA Adducts Deoxyadenosines Intercalating Agents Nucleic Acid Heteroduplexes Oligonucleotides Protons 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Volk D E
Sealy Center for Structural Biology and Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston, Texas 77555-1157, USA. david@nmr.utmb.edu
Rice J S
Luxon B A
Yeh H J
Liang C
Xie G
Sayer J M
Jerina D M
Gorenstein D G
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2000-11-21
Pages
14040-53
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NCI NIH HHS · 1CO6CA59098 · United States
NIEHS NIH HHS · 1P30 ES06676 · United States
NIEHS NIH HHS · ES06839 · United States
Databases
PDB
Analysis Services
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