journal article·2010-12-28

Single Molecule Atomic Force Microscopy Studies of Photosensitized Singlet Oxygen Behavior on a DNA Origami Template

Sarah Helmig, Alexandru Rotaru, Dumitru Arian, Larisa Kovbasyuk, Jacob Arnbjerg, Peter R. Ogilby, Jørgen Kjems, Andriy Mokhir, Flemming Besenbacher, Kurt V. Gothelf

ACS Nano· Volume 4· Issue 12
Publisher page

Abstract

DNA origami, the folding of a long single-stranded DNA sequence (scaffold strand) by hundreds of short synthetic oligonucleotides (staple strands) into parallel aligned helices, is a highly efficient method to form advanced self-assembled DNA-architectures. Since molecules and various materials can be conjugated to each of the short staple strands, the origami method offers a unique possibility of arranging molecules and materials in well-defined positions on a structured surface. Here we combine the action of light with AFM and DNA nanostructures to study the production of singlet oxygen from a single photosensitizer molecule conjugated to a selected DNA origami staple strand on an origami structure. We demonstrate a distance-dependent oxidation of organic moieties incorporated in specific positions on DNA origami by singlet oxygen produced from a single photosensitizer located at the center of each origami.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery · Plasmonic and Surface Plasmon Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Center for DNA Nanotechnology (CDNA) at the Interdisciplinary Nanoscience Center (iNANO)

Department of Chemistry

Institute of Inorganic Chemistry, Ruprecht-Karls University, Heidelberg, Germany

Center for Oxygen Microscopy and Imaging

Department of Molecular Biology

Department of Physics and Astronomy

References (28)

Show source-provided references
1. Rothemund P. W. K. · Nature · 2006 · 440 · 29710.1038/nature04586 ↗
2. Andersen E. S. · ACS Nano · 2008 · 2 · 121310.1021/nn800215j ↗
3. Ke Y. · Nano Lett. · 2009 · 9 · 244510.1021/nl901165f ↗
4. Andersen E. S. · Nature · 2009 · 459 · 7310.1038/nature07971 ↗
5. Douglas S. M. · Nature · 2009 · 459 · 41410.1038/nature08016 ↗
6. Yan H. · Science · 2003 · 301 · 188210.1126/science.1089389 ↗
7. Kuzuya A. · Chembiochem · 2009 · 10 · 181110.1002/cbic.200900229 ↗
8. Voigt N. V. · Nature Nanotechnol. · 2010 · 5 · 20010.1038/nnano.2010.5 ↗
9. Kuzyk A. · Nanotechnology · 2009 · 20 · 23530510.1088/0957-4484/20/23/235305 ↗
10. Endo M. · J. Am. Chem. Soc. · 2010 · 132 · 159210.1021/ja907649w ↗
11. Pal S. · Angew. Chem., Int. Ed. · 2010 · 49 · 270010.1002/anie.201000330 ↗
12. Ding B. Q. · J. Am. Chem. Soc. · 2010 · 132 · 324810.1021/ja9101198 ↗
13. Steinhauer C. · Angew. Chem., Int. Ed. · 2009 · 48 · 887010.1002/anie.200903308 ↗
14. Maune H. T. · Nat. Nanotechnol. · 2010 · 5 · 6110.1038/nnano.2009.311 ↗
15. Ke Y. G. · Science · 2008 · 319 · 18010.1126/science.1150082 ↗
16. Rinker S. · Nat. Nanotechnol. · 2008 · 3 · 41810.1038/nnano.2008.164 ↗
17. Schweitzer C. · Chem. Rev. · 2003 · 103 · 168510.1021/cr010371d ↗
18. Ogilby P. R. · Chem. Soc. Rev. · 2010 · 39 · 318110.1039/b926014p ↗
19. Naito K. · J. Phys. Chem. C · 2008 · 112 · 104810.1021/jp076335l ↗
20. Arian D. · Chem.—Eur. J. · 2010 · 16 · 28810.1002/chem.200902377 ↗
21. Winfree E. · Nature · 1998 · 394 · 53910.1038/28998 ↗
22. Li H. Y. · J. Am. Chem. Soc. · 2004 · 126 · 41810.1021/ja0383367 ↗
23. Rotaru A. · Angew. Chem., Int. Ed. · 2007 · 46 · 618010.1002/anie.200700641 ↗
24. Kautsky H. · Naturwissenschaften · 1931 · 19 · 104310.1007/BF01516190 ↗
25. Skovsen E. · J. Phys. Chem. B · 2005 · 109 · 857010.1021/jp051163i ↗
26. Hatz S. · Photochem. Photobiol. · 2008 · 84 · 128410.1111/j.1751-1097.2008.00359.x ↗
27. Davies M. J. · Biochem. Biophys. Res. Commun. · 2003 · 305 · 76110.1016/S0006-291X(03)00817-9 ↗
28. Tsushima M. · Anal. Chem. · 1994 · 66 · 455110.1021/ac00096a024 ↗