Abstract

DNA has recently emerged as a promising material for the construction of nanosized architectures. Chemically modified DNA has been suggested to be an important component of such architectural building blocks. We have designed and synthesized a novel H-shaped DNA oligonucleotide dimer that is cross-linked with a structurally rigid linker composed of phenylene and ethynylene groups. A rotatable DNA unit was constructed through the self-assembly of this H-shaped DNA component and two complementary DNA oligonucleotides. In addition to the rotatable unit, a locked DNA unit containing two H-shaped DNA components was also constructed. As an example of an extended locked structure, a hexagonal DNA origami dimer and oligomer were constructed by using H-shaped DNA as linkers.

Highlights

  • DNA is a powerful tool that can be used to create nanosized architectures and devices because of its synthetic accessibility and ability to self-assemble (1–6)

  • Various types of DNA–rigid-molecule conjugates have been reported (12–17). In these cases, the rigid linker is connected to the flexible phosphodiester backbone of the DNA oligomer

  • In our DNA unit design, each terminal of the rigid molecule, which is composed of phenylene and ethynylene groups, is joined through a triple bond at the 5 -position of the uridine base located in the middle of the DNA duplexes (Figure 1B)

Read more

Summary

Introduction

DNA is a powerful tool that can be used to create nanosized architectures and devices because of its synthetic accessibility and ability to self-assemble (1–6). For assembling the hexagonal DNA origami, two hexagonal origami monomers, Hex 1 and Hex 2 (5 nM), with four connection strands at the D- and A-edges, respectively, were annealed with H-shaped DNA (H4 linker, 6–8 equiv) from 40 to 15◦ C at a rate of −1.0◦ C/min. (2) After the first elongation, the support was removed from the synthesizer, and a coupling reaction between two reactive alkynes (an oligonucleotide on the support and a modified monomeric nucleotide in solution) was performed by using a solid-phase Glaser reaction (Scheme 1, step A).

Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.