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G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch
Nucleic acid based molecular device is a developing research field which attracts great interests in material for building machinelike nanodevices. G-quadruplex, as a new type of DNA secondary structures, can be harnessed to construct molecular device owing to its rich structural polymorphism. Herei...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438431/ https://www.ncbi.nlm.nih.gov/pubmed/25990684 http://dx.doi.org/10.1038/srep10479 |
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author | Guan, Ai-Jiao Shen, Meng-Jie Xiang, Jun-Feng Zhang, En-Xuan Li, Qian Sun, Hong-Xia Wang, Li-Xia Xu, Guang-Zhi Tang, Ya-Lin Xu, Li-Jin Gong, Han-Yuan |
author_facet | Guan, Ai-Jiao Shen, Meng-Jie Xiang, Jun-Feng Zhang, En-Xuan Li, Qian Sun, Hong-Xia Wang, Li-Xia Xu, Guang-Zhi Tang, Ya-Lin Xu, Li-Jin Gong, Han-Yuan |
author_sort | Guan, Ai-Jiao |
collection | PubMed |
description | Nucleic acid based molecular device is a developing research field which attracts great interests in material for building machinelike nanodevices. G-quadruplex, as a new type of DNA secondary structures, can be harnessed to construct molecular device owing to its rich structural polymorphism. Herein, we developed a switching system based on G-quadruplexes and methylazacalix[6]pyridine (MACP6). The induced circular dichroism (CD) signal of MACP6 was used to monitor the switch controlled by temperature or pH value. Furthermore, the CD titration, Job-plot, variable temperature CD and (1)H-NMR experiments not only confirmed the binding mode between MACP6 and G-quadruplex, but also explained the difference switching effect of MACP6 and various G-quadruplexes. The established strategy has the potential to be used as the chiral probe for specific G-quadruplex recognition. |
format | Online Article Text |
id | pubmed-4438431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44384312015-06-01 G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch Guan, Ai-Jiao Shen, Meng-Jie Xiang, Jun-Feng Zhang, En-Xuan Li, Qian Sun, Hong-Xia Wang, Li-Xia Xu, Guang-Zhi Tang, Ya-Lin Xu, Li-Jin Gong, Han-Yuan Sci Rep Article Nucleic acid based molecular device is a developing research field which attracts great interests in material for building machinelike nanodevices. G-quadruplex, as a new type of DNA secondary structures, can be harnessed to construct molecular device owing to its rich structural polymorphism. Herein, we developed a switching system based on G-quadruplexes and methylazacalix[6]pyridine (MACP6). The induced circular dichroism (CD) signal of MACP6 was used to monitor the switch controlled by temperature or pH value. Furthermore, the CD titration, Job-plot, variable temperature CD and (1)H-NMR experiments not only confirmed the binding mode between MACP6 and G-quadruplex, but also explained the difference switching effect of MACP6 and various G-quadruplexes. The established strategy has the potential to be used as the chiral probe for specific G-quadruplex recognition. Nature Publishing Group 2015-05-20 /pmc/articles/PMC4438431/ /pubmed/25990684 http://dx.doi.org/10.1038/srep10479 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Guan, Ai-Jiao Shen, Meng-Jie Xiang, Jun-Feng Zhang, En-Xuan Li, Qian Sun, Hong-Xia Wang, Li-Xia Xu, Guang-Zhi Tang, Ya-Lin Xu, Li-Jin Gong, Han-Yuan G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title | G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title_full | G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title_fullStr | G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title_full_unstemmed | G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title_short | G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
title_sort | g-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: en route to multiplex controlled molecular switch |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438431/ https://www.ncbi.nlm.nih.gov/pubmed/25990684 http://dx.doi.org/10.1038/srep10479 |
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