Triple-Stranded DNA As a Structural Element in DNA Origami
Source abstract
Abstract
Molecular self-assembly with DNA origami offers an attractive route to fabricate arbitrary three-dimensional nanostructures. In DNA origami, B-form double-helical DNA domains (dsDNA) are commonly linked with covalent phosphodiester strand crossovers to build up three-dimensional objects. To expand the palette of structural motifs in DNA origami, here we describe hybrid duplex-triplex DNA motifs as pH-dependent building blocks in DNA origami. We investigate design rules for incorporating triplex forming oligonucleotides and noncanonical duplex-triplex crossovers in multilayer DNA origami objects. We use single-particle cryoelectron microscopy to elucidate the structural basis of triplex domains and of duplex-triplex crossovers. We find that duplex-triplex crossovers can complement and fully replace the canonical duplex-duplex crossovers within DNA origami objects, for example, to increase the crossover density for potentially greater rigidity and reduced interhelical spacing, and to create connections at sites where conventional crossovers may be undesirable. We also show the pH-induced formation of a DNA origami object stabilized entirely by triplex-mediated strand crossovers.
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
Department of Biosciences, School of Natural Sciences and Munich Institute of Biomedical Engineering, Technical University Munich (TUM), Munich, Garching 85748, Germany
Funding
Deutsche Forschungsgemeinschaft · H2020 Future and Emerging Technologies · H2020 European Research Council · Nederlandse Organisatie voor Wetenschappelijk Onderzoek
References (37)
Show source-provided references
1. 10.1126/sciadv.150120910.1126/sciadv.1501209 ↗
2. 10.1038/s41576-019-0175-610.1038/s41576-019-0175-6 ↗
3. 10.1073/pnas.140886911210.1073/pnas.1408869112 ↗
4. 10.1038/ncomms1241410.1038/ncomms12414 ↗
5. 10.1016/0378-1119(93)90054-710.1016/0378-1119(93)90054-7 ↗
6. 10.1016/0006-3002(57)90091-410.1016/0006-3002(57)90091-4 ↗
7. 10.1021/bi00104a03110.1021/bi00104a031 ↗
8. 10.1021/bi00153a02110.1021/bi00153a021 ↗
9. 10.1089/15454570332286082510.1089/154545703322860825 ↗
10. 10.1021/ja500619w10.1021/ja500619w ↗
11. 10.1021/bi992630n10.1021/bi992630n ↗
12. 10.1021/bi010666l10.1021/bi010666l ↗
13. 10.1002/anie.20046078910.1002/anie.200460789 ↗
14. 10.1021/ja045718j10.1021/ja045718j ↗
15. 10.1021/ja805945r10.1021/ja805945r ↗
16. 10.1021/acs.nanolett.5b0212310.1021/acs.nanolett.5b02123 ↗
17. 10.1021/acsnano.9b0185710.1021/acsnano.9b01857 ↗
18. 10.1002/chem.20150503010.1002/chem.201505030 ↗
19. 10.1039/C6CC03695C10.1039/C6CC03695C ↗
20. 10.1021/acsnano.9b0102510.1021/acsnano.9b01025 ↗
21. 10.1021/jacs.9b0416810.1021/jacs.9b04168 ↗
22. 10.1038/s41467-021-24675-810.1038/s41467-021-24675-8 ↗
23. 10.1038/s41467-020-20020-710.1038/s41467-020-20020-7 ↗
24. 10.1038/s41586-018-0332-710.1038/s41586-018-0332-7 ↗
25. 10.1093/nar/gkp43610.1093/nar/gkp436 ↗
26. 10.1021/acs.nanolett.5b0146110.1021/acs.nanolett.5b01461 ↗
27. 10.1126/science.122991910.1126/science.1229919 ↗
28. 10.1002/cbic.20170037710.1002/cbic.201700377 ↗
29. 10.1038/nature2465010.1038/nature24650 ↗
30. 10.7554/eLife.4216610.7554/eLife.42166 ↗
31. 10.1038/nmeth.419310.1038/nmeth.4193 ↗
32. 10.1016/j.jsb.2015.08.00810.1016/j.jsb.2015.08.008 ↗
33. 10.1038/s42003-019-0437-z10.1038/s42003-019-0437-z ↗
34. 10.7554/eLife.3686110.7554/eLife.36861 ↗
35. 10.1002/jcc.2008410.1002/jcc.20084 ↗
36. 10.1093/nar/gkw15510.1093/nar/gkw155 ↗
37. 10.1006/jmbi.2001.498710.1006/jmbi.2001.4987 ↗