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Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution
Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer targets. Here we show that four-repeat human telomeric DNA sequences can adopt two different intramolecular G-quadruplex folds in K(+) solution. The two structures contain the (3+1) G-tetrad core, in w...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635308/ https://www.ncbi.nlm.nih.gov/pubmed/17040899 http://dx.doi.org/10.1093/nar/gkl726 |
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author | Phan, Anh Tuân Luu, Kim Ngoc Patel, Dinshaw J. |
author_facet | Phan, Anh Tuân Luu, Kim Ngoc Patel, Dinshaw J. |
author_sort | Phan, Anh Tuân |
collection | PubMed |
description | Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer targets. Here we show that four-repeat human telomeric DNA sequences can adopt two different intramolecular G-quadruplex folds in K(+) solution. The two structures contain the (3+1) G-tetrad core, in which three G-tracts are oriented in one direction and the fourth in the opposite direction, with one double-chain-reversal and two edgewise loops, but involve different loop arrangements. This result indicates the robustness of the (3+1) core G-quadruplex topology, thereby suggesting it as an important platform for structure-based drug design. Our data also support the view that multiple human telomeric G-quadruplex conformations coexist in K(+) solution. Furthermore, even small changes to flanking sequences can perturb the equilibrium between different coexisting G-quadruplex forms. |
format | Text |
id | pubmed-1635308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-16353082006-11-29 Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution Phan, Anh Tuân Luu, Kim Ngoc Patel, Dinshaw J. Nucleic Acids Res Structural Biology Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer targets. Here we show that four-repeat human telomeric DNA sequences can adopt two different intramolecular G-quadruplex folds in K(+) solution. The two structures contain the (3+1) G-tetrad core, in which three G-tracts are oriented in one direction and the fourth in the opposite direction, with one double-chain-reversal and two edgewise loops, but involve different loop arrangements. This result indicates the robustness of the (3+1) core G-quadruplex topology, thereby suggesting it as an important platform for structure-based drug design. Our data also support the view that multiple human telomeric G-quadruplex conformations coexist in K(+) solution. Furthermore, even small changes to flanking sequences can perturb the equilibrium between different coexisting G-quadruplex forms. Oxford University Press 2006-11 2006-10-12 /pmc/articles/PMC1635308/ /pubmed/17040899 http://dx.doi.org/10.1093/nar/gkl726 Text en © 2006 The Author(s) |
spellingShingle | Structural Biology Phan, Anh Tuân Luu, Kim Ngoc Patel, Dinshaw J. Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title | Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title_full | Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title_fullStr | Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title_full_unstemmed | Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title_short | Different loop arrangements of intramolecular human telomeric (3+1) G-quadruplexes in K(+) solution |
title_sort | different loop arrangements of intramolecular human telomeric (3+1) g-quadruplexes in k(+) solution |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1635308/ https://www.ncbi.nlm.nih.gov/pubmed/17040899 http://dx.doi.org/10.1093/nar/gkl726 |
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