G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: En route to multiplex controlled molecular switch

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Abstract

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.

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Guan, A. J., Shen, M. J., Xiang, J. F., Zhang, E. X., Li, Q., Sun, H. X., … Gong, H. Y. (2015). G-quadruplex induced chirality of methylazacalix[6]pyridine via unprecedented binding stoichiometry: En route to multiplex controlled molecular switch. Scientific Reports, 5. https://doi.org/10.1038/srep10479

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