Cargando…

1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine

[Image: see text] The oligodeoxynucleotide 5′-CGCATXGAATCC-3′·5′-GGATTCAATGCG-3′ containing 1,N(2)-etheno-2′-deoxyguanosine (1,N(2)-εdG) opposite deoxyadenosine (named the 1,N(2)-εdG·dA duplex) models the mismatched adenine product associated with error-prone bypass of 1,N(2)-εdG by the Sulfolobus s...

Descripción completa

Detalles Bibliográficos
Autores principales: Shanmugam, Ganesh, Kozekov, Ivan D., Guengerich, F. Peter, Rizzo, Carmelo J., Stone, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2011
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138413/
https://www.ncbi.nlm.nih.gov/pubmed/21675798
http://dx.doi.org/10.1021/tx200089v
_version_ 1782208380534784000
author Shanmugam, Ganesh
Kozekov, Ivan D.
Guengerich, F. Peter
Rizzo, Carmelo J.
Stone, Michael P.
author_facet Shanmugam, Ganesh
Kozekov, Ivan D.
Guengerich, F. Peter
Rizzo, Carmelo J.
Stone, Michael P.
author_sort Shanmugam, Ganesh
collection PubMed
description [Image: see text] The oligodeoxynucleotide 5′-CGCATXGAATCC-3′·5′-GGATTCAATGCG-3′ containing 1,N(2)-etheno-2′-deoxyguanosine (1,N(2)-εdG) opposite deoxyadenosine (named the 1,N(2)-εdG·dA duplex) models the mismatched adenine product associated with error-prone bypass of 1,N(2)-εdG by the Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) and by Escherichia coli polymerases pol I exo(–) and pol II exo(–). At pH 5.2, the T(m) of this duplex was increased by 3 °C as compared to the duplex in which the 1,N(2)-εdG lesion is opposite dC, and it was increased by 2 °C compared to the duplex in which guanine is opposite dA (the dG·dA duplex). A strong NOE between the 1,N(2)-εdG imidazole proton and the anomeric proton of the attached deoxyribose, accompanied by strong NOEs to the minor groove A(20) H2 proton and the mismatched A(19) H2 proton from the complementary strand, establish that 1,N(2)-εdG rotated about the glycosyl bond from the anti to the syn conformation. The etheno moiety was placed into the major groove. This resulted in NOEs between the etheno protons and T(5) CH(3). A strong NOE between A(20) H2 and A(19) H2 protons established that A(19), opposite to 1,N(2)-εdG, adopted the anti conformation and was directed toward the helix. The downfield shifts of the A(19) amino protons suggested protonation of dA. Thus, the protonated 1,N(2)-εdG·dA base pair was stabilized by hydrogen bonds between 1,N(2)-εdG N1 and A(19) N1H(+) and between 1,N(2)-εdG O(9) and A(19)N(6)H. The broad imino proton resonances for the 5′- and 3′-flanking bases suggested that both neighboring base pairs were perturbed. The increased stability of the 1,N(2)-εdG·dA base pair, compared to that of the 1,N(2)-εdG·dC base pair, correlated with the mismatch adenine product observed during the bypass of 1,N(2)-εdG by the Dpo4 polymerase, suggesting that stabilization of this mismatch may be significant with regard to the biological processing of 1,N(2)-εdG.
format Online
Article
Text
id pubmed-3138413
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-31384132011-07-18 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine Shanmugam, Ganesh Kozekov, Ivan D. Guengerich, F. Peter Rizzo, Carmelo J. Stone, Michael P. Chem Res Toxicol [Image: see text] The oligodeoxynucleotide 5′-CGCATXGAATCC-3′·5′-GGATTCAATGCG-3′ containing 1,N(2)-etheno-2′-deoxyguanosine (1,N(2)-εdG) opposite deoxyadenosine (named the 1,N(2)-εdG·dA duplex) models the mismatched adenine product associated with error-prone bypass of 1,N(2)-εdG by the Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) and by Escherichia coli polymerases pol I exo(–) and pol II exo(–). At pH 5.2, the T(m) of this duplex was increased by 3 °C as compared to the duplex in which the 1,N(2)-εdG lesion is opposite dC, and it was increased by 2 °C compared to the duplex in which guanine is opposite dA (the dG·dA duplex). A strong NOE between the 1,N(2)-εdG imidazole proton and the anomeric proton of the attached deoxyribose, accompanied by strong NOEs to the minor groove A(20) H2 proton and the mismatched A(19) H2 proton from the complementary strand, establish that 1,N(2)-εdG rotated about the glycosyl bond from the anti to the syn conformation. The etheno moiety was placed into the major groove. This resulted in NOEs between the etheno protons and T(5) CH(3). A strong NOE between A(20) H2 and A(19) H2 protons established that A(19), opposite to 1,N(2)-εdG, adopted the anti conformation and was directed toward the helix. The downfield shifts of the A(19) amino protons suggested protonation of dA. Thus, the protonated 1,N(2)-εdG·dA base pair was stabilized by hydrogen bonds between 1,N(2)-εdG N1 and A(19) N1H(+) and between 1,N(2)-εdG O(9) and A(19)N(6)H. The broad imino proton resonances for the 5′- and 3′-flanking bases suggested that both neighboring base pairs were perturbed. The increased stability of the 1,N(2)-εdG·dA base pair, compared to that of the 1,N(2)-εdG·dC base pair, correlated with the mismatch adenine product observed during the bypass of 1,N(2)-εdG by the Dpo4 polymerase, suggesting that stabilization of this mismatch may be significant with regard to the biological processing of 1,N(2)-εdG. American Chemical Society 2011-06-16 2011-07-18 /pmc/articles/PMC3138413/ /pubmed/21675798 http://dx.doi.org/10.1021/tx200089v Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Shanmugam, Ganesh
Kozekov, Ivan D.
Guengerich, F. Peter
Rizzo, Carmelo J.
Stone, Michael P.
1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title_full 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title_fullStr 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title_full_unstemmed 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title_short 1,N(2)-Etheno-2′-deoxyguanosine Adopts the syn Conformation about the Glycosyl Bond When Mismatched with Deoxyadenosine
title_sort 1,n(2)-etheno-2′-deoxyguanosine adopts the syn conformation about the glycosyl bond when mismatched with deoxyadenosine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138413/
https://www.ncbi.nlm.nih.gov/pubmed/21675798
http://dx.doi.org/10.1021/tx200089v
work_keys_str_mv AT shanmugamganesh 1n2etheno2deoxyguanosineadoptsthesynconformationabouttheglycosylbondwhenmismatchedwithdeoxyadenosine
AT kozekovivand 1n2etheno2deoxyguanosineadoptsthesynconformationabouttheglycosylbondwhenmismatchedwithdeoxyadenosine
AT guengerichfpeter 1n2etheno2deoxyguanosineadoptsthesynconformationabouttheglycosylbondwhenmismatchedwithdeoxyadenosine
AT rizzocarmeloj 1n2etheno2deoxyguanosineadoptsthesynconformationabouttheglycosylbondwhenmismatchedwithdeoxyadenosine
AT stonemichaelp 1n2etheno2deoxyguanosineadoptsthesynconformationabouttheglycosylbondwhenmismatchedwithdeoxyadenosine