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Photoresponsive Formation of an Intermolecular Minimal G‐Quadruplex Motif
Authors:Julie Thevarpadam  Irene Bessi  Oliver Binas  Dr Diana P N Gonçalves  Dr Chavdar Slavov  Dr Hendrik R A Jonker  Dr Christian Richter  Prof?Dr Josef Wachtveitl  Prof?Dr Harald Schwalbe  Prof?Dr Alexander Heckel
Institution:1. Goethe University Frankfurt, Institute for Organic Chemistry and Chemical Biology, Buchmann Institute for Molecular Life Sciences, Frankfurt, Germany;2. Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Frankfurt, Germany;3. Institute for Physical and Theoretical Chemistry, Frankfurt, Germany;4. http://schwalbe.org.chemie.uni‐frankfurt.de;5. http://photochem.uni‐frankfurt.de
Abstract:The ability of three different bifunctional azobenzene linkers to enable the photoreversible formation of a defined intermolecular two‐tetrad G‐quadruplex upon UV/Vis irradiation was investigated. Circular dichroism and NMR spectroscopic data showed the formation of G‐quadruplexes with K+ ions at room temperature in all three cases with the corresponding azobenzene linker in an E conformation. However, only the parapara‐substituted azobenzene derivative enables photoswitching between a nonpolymorphic, stacked, tetramolecular G‐quadruplex and an unstructured state after EZ isomerization.
Keywords:azobenzene  DNA structures  G-quadruplexes  IR spectroscopy  NMR spectroscopy
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