Covalent Linkage of One-Dimensional DNA Arrays Bonded by Paranemic Cohesion

ACS Nano. 2015 Oct 27;9(10):10304-12. doi: 10.1021/acsnano.5b04335. Epub 2015 Sep 11.

Abstract

The construction of DNA nanostructures from branched DNA motifs, or tiles, typically relies on the use of sticky-ended cohesion, owing to the specificity and programmability of DNA sequences. The stability of such constructs when unligated is restricted to a specific range of temperatures, owing to the disruption of base pairing at elevated temperatures. Paranemic (PX) cohesion was developed as an alternative to sticky ends for the cohesion of large topologically closed species that could be purified reliably on denaturing gels. However, PX cohesion is also of limited stability. In this work, we added sticky-ended interactions to PX-cohesive complexes to create interlocked complexes by functionalizing the sticky ends with psoralen, which can form cross-links between the two strands of a double helix. We were able to reinforce the stability of the constructs by creating covalent linkages between the 3'-ends and 5'-ends of the sticky ends; the sticky ends were added to double crossover domains via 3'-3' and 5'-5' linkages. Catenated arrays were obtained either by enzymatic ligation or by UV cross-linking. We have constructed finite-length one-dimensional arrays linked by interlocking loops and have positioned streptavidin-gold particles on these constructs.

Keywords: 3′,3′ and 5′,5′ linkages; UV cross-linking; catenanes; ligated DNA constructs; one-dimensional DNA arrays; paranemic cohesion; topological linkage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Pairing
  • DNA Topoisomerases, Type I / metabolism
  • DNA, Catenated / chemistry*
  • DNA, Catenated / metabolism
  • Escherichia coli / enzymology
  • Gold / chemistry
  • Models, Molecular
  • Nanostructures / chemistry*
  • Nanostructures / ultrastructure
  • Nanotechnology / methods
  • Nucleic Acid Conformation
  • Nucleotide Motifs
  • Oligonucleotide Array Sequence Analysis*

Substances

  • DNA, Catenated
  • Gold
  • DNA Topoisomerases, Type I