Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-zzh7m Total loading time: 0 Render date: 2024-04-27T00:53:06.278Z Has data issue: false hasContentIssue false

13 - Not just plain vanilla DNA nanotechnology: other pairings, other backbones

Published online by Cambridge University Press:  05 December 2015

Nadrian C. Seeman
Affiliation:
New York University
Get access

Summary

Up to this point, we have been talking largely about Watson–Crick double helical DNA. No variations in the base-pairing and no variations in the backbone. Here we are going to discuss just a little bit of the work that is going on with other DNA structures, work that entails non-DNA backbones, and other species organized by DNA nanoconstructs. This chapter is not meant to be a comprehensive review of variations on the theme of either DNA nor its interactions with other species, just a taste to stimulate the reader to pursue other materials on her own.

Paukstelis DNA structure. Perhaps the first place to start is DNA, but DNA that is not simply Watson–Crick. A robust motif discovered in a single-crystal structure is shown in Figure 13-1. This motif contains three conventional nucleotide pairs and three parallel pairs, consisting of one A–G pair and two G–G pairs. This overall motif is shown in stereo in Figure 13-2. A salient feature of the structure is that it crystallizes in a hexagonal space group with a cavity whose volume is 300 Å3, which is shown in stereo in Figure 13-3a. The robustness of the motif is demonstrated by the fact that the Watson–Crick portion of the motif can be extended by 10 nucleotide pairs, yet the space group remains the same. Although the resolution of the crystal decreases somewhat, the cavity is greatly expanded by this expansion, so its volume is now increased markedly, as shown in Figure 13-3b.

Triplex DNA. In addition to the simple double helical motif, there are other helical motifs that have been characterized. The earliest of these was the DNA triplex, wherein a pyrimidine–purine–pyrimidine structure was formed (see Figures 2-4 and 2-5). There are a number of utilities that one can imagine for such systems in DNA constructs. Without disrupting the double helix, it is possible to address specifically designed locations within the assembly by adding a triplex-forming oligonucleotide (TFO). One could imagine tethering both small molecules and macromolecules to DNA constructs by the use of triplex associations. An example of triplex DNA added to DNA tensegrity-triangle crystals (see Chapter 7, especially Figure 7-23) is shown schematically in Figure 13-4; crystals to which triplex molecules containing dyes have been attached are shown in Figure 13-5.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2016

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

13.1 Paukstelis, P., Nowakowski, J., Birktoft, J.J., Seeman, N.C., The Crystal Structure of a Continuous Three-Dimensional DNA Lattice. Chem. Biol. 11, 1119–1126 (2004).CrossRefGoogle ScholarPubMed
13.2 Felsenfeld, G., Davies, D.R., Rich, A., Formation of a Three-Stranded Polynucleotide Molecule. J. Am. Chem. Soc. 79, 2023–2024 (1957).CrossRefGoogle Scholar
13.3 Rusling, D.A., Chandrasekaran, A.R., Ohayon, Y., Brown, T., Fox, K.R., Sha, R., Mao, C., Seeman, N.C., Functionalizing Designer DNA Crystals with a Triple-Helical Veneer. Angew. Chemie Int. Ed. 53, 4060–4063 (2014).CrossRefGoogle ScholarPubMed
13.4 Gellert, M., Gellert, M.F., Davies, D.R., Helix Formation by Guanylic Acid. Proc. Nat. Acad. Sci. (USA) 48, 2013–2018 (1962).CrossRefGoogle ScholarPubMed
13.5 Sen, D., Gilbert, W., Novel DNA Superstructures Formed by Telomere-Like Oligomers. Biochem. 31, 65–70 (1992).CrossRefGoogle ScholarPubMed
13.6 Venczel, E.A., Sen, D., Synapsable DNA. J. Mol. Biol. 257, 210–224 (1996).CrossRefGoogle ScholarPubMed
13.7 Yatsunyk, L.A., Piétrement, O., Albrecht, D., Tran, P.L.T., Renciuk, D., Sugiyama, H., Arbona, J.-M., Aimé, J.P., Mergny, J.-L., Guided Assembly of Tetramolecular G-Quadruplexes. ACSNano 7, 5701–5710 (2013).Google ScholarPubMed
13.8 Marsh, T.C., Vesenka, J., Henderson, E., A New DNA Nanostructure, the G-Wire, Imaged by Scanning Probe Microscopy. Nucl. Acids Res. 23, 696–700 (1995).CrossRefGoogle ScholarPubMed
13.9 Saphir, E., Sagiv, L., Molotsky, T., Kotlyar, A.B., Felice, R. Di, Porath, D., Electronic Structure of G4-DNA by Scanning Tunneling Spectroscopy. J. Phys. Chem. C 114, 22079–22084 (2010).Google Scholar
13.10 Borovok, N., Iram, N., Zikich, D., Ghabboun, J., Livshits, G.I., Porath, D., Kotlyar, A.B., Assembling of G-Strand into Novel Tetra-Molecular Parallel G4-DNA Nanostructures Using Avidin-Biotin Recognition. Nucl. Acids Res. 36, 5050–5060 (2008).CrossRefGoogle ScholarPubMed
13.11 Modi, S., Nizak, C., Surana, S., Halder, S., Krishnan, Y., Two DNA Machines Map pH Changes Along Intersecting Endocytic Pathways in the Same Cell. Nature Nanotech. 6, 459–467 (2013).Google Scholar
13.12 Wang, H., Gate, R.J. Di, Seeman, N.C., The Construction of an RNA Knot and Its Role in Demonstrating That E. Coli DNA Topoisomerase III is an RNA Topoisomerase. In Structure, Motion, Interaction and Expression of Biological Macromolecules, ed. Sarma, R.H., Sarma, M.H., New York, Adenine Press, pp. 103–116 (1998).Google Scholar
13.13 Seeman, N.C., Maestre, M.F., Ma, R.-I., Kallenbach, N.R., Physical Characterization of a Nucleic Acid Junction. In Progress in Clinical and Biological Research, Vol. 172A: The Molecular Basis of Cancer, ed. Rein, R., New York, Alan R. Liss, pp. 99–108 (1985).Google Scholar
13.14 Xu, D., Shen, W., Guo, R., Xu, Y., Peng, W., Sima, J., Yang, J., Sharov, A., Srikantan, S., Yang, J., Fox, D. III, Qian, Y., Martindale, J.L., Piao, Y., Machamer, J., Joshi, S.R., Mohanty, S., Shaw, A.C., Lloyd, T.E., Brown, G.W., Ko, M.S.H., Gorospe, M., Zou, S., Wang, W., Top3β is an RNA Topoisomerase That Works with Fragile X Syndrome Protein to Promote Synapse Formation. Nature Neurosci. 16, 1238–1250 (2013).CrossRefGoogle ScholarPubMed
13.15 Afonin, K.A., Cieply, D.J, Leontis, N.B., Specific RNA Assembly with Paranemic Motifs. J. Am. Chem. Soc. 130, 93–102 (2008).CrossRefGoogle ScholarPubMed
13.16 Dibrov, S.M., McLean, J., Parsons, J., Hermann, T., Self-Assembling RNA Square. Proc. Nat. Acad. Sci. (USA) 108, 6405–6408 (2011).CrossRefGoogle ScholarPubMed
13.17 Chworos, A., Severcan, I., Koyfman, A.Y., Weinkam, P., Oroudjem, E., Hansma, H.G., Jaeger, L., Building Programmable Jigsaw Puzzles with RNA. Science 306, 2068–2072 (2004).CrossRefGoogle ScholarPubMed
13.18 Alfonin, K.A., Bindewald, E., Yaghoubian, A.J., Voss, N., Jocovetty, E., Shapiro, B.A., Jaeger, L., In Vitro Assembly of Cubic RNA-Based Scaffolds Designed in Silico. Nature Nanotech. 5, 676–682 (2010).Google Scholar
13.19 Delebecque, C.J., Lindner, A.B., Silver, P.A., Aldaye, F.A., Organization of Intracellular Reactions with Rationally Designed RNA Assemblies. Science 333, 470–474 (2011).CrossRefGoogle ScholarPubMed
13.20 Geary, C., Rothemund, P.W.K., Andersen, E.S., A Single-Stranded Architecture for Cotranscriptional Folding of RNA Nanostructures. Science 345, 799–804 (2014).CrossRefGoogle ScholarPubMed
13.21 Egholm, M., Buchardt, O., Nielsen, P.E., Berg, R.H., Peptide Nucleic Acids (PNA): Oligonucleotide Analogues with an Achiral Peptide Backbone. J. Am. Chem. Soc. 114, 1895–1897 (1992).CrossRefGoogle Scholar
13.22 Lukeman, P.S., Mittal, A., Seeman, N.C., Two Dimensional PNA/DNA Arrays: Estimating the Helicity of Unusual Nucleic Acid Polymers. Chem. Comm. 2004, 1694–1695 (2004).Google Scholar
13.23 Gnapareddy, B., Kim, J.A., Dugasani, S.R., Tandon, A., Kim, B., Bashar, S., Choi, J.A., Joe, G.H., Kim, T., Ha, T.H., Park, S.H., Fabrication and Characterization of PNA-DNA Hybrid Nanostructure. RSC Adv. 4, 35554–35558 (2014).CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×