Light-driven chiroptical photoswitchable DNA assemblies mediated by bioinspired photoresponsive molecules
Source abstract
Abstract
We show that the incorporation of chiral bioinspired photochromic compounds into inherently chiral DNA matrices enables the building of smart nanoscale photoswitchable chiroptical assemblies tunable over a wide range of wavelengths. Moreover, the use of light as external trigger affords precise control of the resulting hybrid DNA nanostructures, and their chiroptical activities can be spatially modulated without photochemical fatigue.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Advanced Materials Engineering and Modelling Group
Faculty of Chemistry
Wroclaw University of Science and Technology
50-370 Wroclaw
Poland
Department of Bioorganic Chemistry
Funding
Narodowe Centrum Nauki
References (28)
Show source-provided references
1. Kamiya · Acc. Chem. Res. · 2014 · 47 · 166310.1021/ar400308f ↗
2. Pijper · Soft Matter · 2008 · 4 · 134910.1039/b801886c ↗
3. Pinheiro · Nat. Nanotechnol. · 2011 · 6 · 76310.1038/nnano.2011.187 ↗
4. Zhao · Nat. Chem. · 2017 · 9 · 25010.1038/nchem.2668 ↗
5. Song · Chem. Commun. · 2010 · 46 · 728310.1039/c0cc01312a ↗
6. Zhao · Chem. Commun. · 2016 · 52 · 136510.1039/C5CC08401F ↗
7. Fu · Chem. Commun. · 2016 · 52 · 1005210.1039/C6CC04866H ↗
8. Chung · Proc. Natl. Acad. Sci. U. S. A. · 2015 · 112 · 272910.1073/pnas.1418718112 ↗
9. Kim · Nat. Nanotechnol. · 2017 · 12 · 55110.1038/nnano.2017.42 ↗
10. Mammana · J. Phys. Chem. B · 2011 · 115 · 1158110.1021/jp205893y ↗
11. Kel · Chem. – Eur. J. · 2013 · 19 · 717310.1002/chem.201203915 ↗
12. Kawara · Chem. – Eur. J. · 2017 · 23 · 176310.1002/chem.201605276 ↗
13. Lubbe · Chem. Soc. Rev. · 2017 · 46 · 105210.1039/C6CS00461J ↗
14. Bergen · Nano Lett. · 2016 · 16 · 77310.1021/acs.nanolett.5b04762 ↗
15. Beharry · Chem. Soc. Rev. · 2011 · 40 · 442210.1039/c1cs15023e ↗
16. Deiana · Sci. Rep. · 2016 · 6 · 2860510.1038/srep28605 ↗
17. Deiana · J. Mater. Chem. B · 2017 · 5 · 102810.1039/C6TB02732F ↗
18. Deiana · Phys. Chem. Chem. Phys. · 2017 · 19 · 2127210.1039/C7CP03336B ↗
19. Hahn · Chem. – Eur. J. · 2016 · 22 · 631410.1002/chem.201504934 ↗
20. Grande · Angew. Chem., Int. Ed. · 2017 · 56 · 752010.1002/anie.201702096 ↗
21. Tran · Biochimie · 2011 · 93 · 128810.1016/j.biochi.2011.05.011 ↗
22. Deiana · Biomacromolecules · 2016 · 17 · 360910.1021/acs.biomac.6b01113 ↗
23. Deiana · Phys. Chem. Chem. Phys. · 2015 · 17 · 3031810.1039/C5CP05381A ↗
24. Deiana · ACS Omega · 2017 · 2 · 571510.1021/acsomega.7b00665 ↗
25. Deiana · J. Phys. Chem. Lett. · 2017 · 8 · 591510.1021/acs.jpclett.7b02547 ↗
26. Mohanty · J. Am. Chem. Soc. · 2013 · 135 · 36710.1021/ja309588h ↗
27. Pescitelli · Chem. Soc. Rev. · 2014 · 43 · 521110.1039/C4CS00104D ↗
28. Neidle · J. Med. Chem. · 2016 · 59 · 598710.1021/acs.jmedchem.5b01835 ↗