Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3

Phen-DC3 is a highly promising compound that specifically targets G-quadruplexes, with potent biological effects observed in vivo. We used NMR spectroscopy to solve the structure of the complex formed between Phen-DC3 and an intramolecular G-quadruplex derived from the c-myc promoter. Structural inf...

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Main Authors: Chung, Wan Jun, Heddi, Brahim, Hamon, Florian, Teulade-Fichou, Marie-Paule, Phan, Anh Tuân
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2014
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Online Access:https://hdl.handle.net/10356/102946
http://hdl.handle.net/10220/19192
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1029462020-03-07T12:37:12Z Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3 Chung, Wan Jun Heddi, Brahim Hamon, Florian Teulade-Fichou, Marie-Paule Phan, Anh Tuân School of Physical and Mathematical Sciences DRNTU::Science::Chemistry Phen-DC3 is a highly promising compound that specifically targets G-quadruplexes, with potent biological effects observed in vivo. We used NMR spectroscopy to solve the structure of the complex formed between Phen-DC3 and an intramolecular G-quadruplex derived from the c-myc promoter. Structural information revealed that Phen-DC3 interacts with the quadruplex through extensive π-stacking with guanine bases of the top G-tetrad. On the basis of our structure, modifications are proposed for the development of this compound for selective targeting of a specific G-quadruplex conformation. 2014-04-09T06:16:49Z 2019-12-06T21:02:36Z 2014-04-09T06:16:49Z 2019-12-06T21:02:36Z 2014 2014 Journal Article Chung, W. J., Heddi, B., Hamon, F., Teulade-Fichou, M.-P., & Phan, A. T. (2014). Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3. Angewandte Chemie International Edition, 53(4), 999-1002. 1433-7851 https://hdl.handle.net/10356/102946 http://hdl.handle.net/10220/19192 10.1002/anie.201308063 en Angewandte chemie international edition © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Chemistry
spellingShingle DRNTU::Science::Chemistry
Chung, Wan Jun
Heddi, Brahim
Hamon, Florian
Teulade-Fichou, Marie-Paule
Phan, Anh Tuân
Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
description Phen-DC3 is a highly promising compound that specifically targets G-quadruplexes, with potent biological effects observed in vivo. We used NMR spectroscopy to solve the structure of the complex formed between Phen-DC3 and an intramolecular G-quadruplex derived from the c-myc promoter. Structural information revealed that Phen-DC3 interacts with the quadruplex through extensive π-stacking with guanine bases of the top G-tetrad. On the basis of our structure, modifications are proposed for the development of this compound for selective targeting of a specific G-quadruplex conformation.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Chung, Wan Jun
Heddi, Brahim
Hamon, Florian
Teulade-Fichou, Marie-Paule
Phan, Anh Tuân
format Article
author Chung, Wan Jun
Heddi, Brahim
Hamon, Florian
Teulade-Fichou, Marie-Paule
Phan, Anh Tuân
author_sort Chung, Wan Jun
title Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
title_short Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
title_full Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
title_fullStr Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
title_full_unstemmed Solution structure of a G-quadruplex bound to the bisquinolinium compound Phen-DC3
title_sort solution structure of a g-quadruplex bound to the bisquinolinium compound phen-dc3
publishDate 2014
url https://hdl.handle.net/10356/102946
http://hdl.handle.net/10220/19192
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