Coupling across a DNA helical turn yields a hybrid DNA/organic catenane doubly tailed with functional termini

J Am Chem Soc. 2008 Aug 20;130(33):10882-3. doi: 10.1021/ja8041096. Epub 2008 Jul 29.

Abstract

We describe the synthesis of a hybrid DNA/organic macrocycle that is prepared by formation of an amide linkage across one full turn of DNA. Formation of a catenane proved that the linkage crossed a turn rather than running along the phosphodiester backbone contour. The product, a doubly tailed catenane, contains 5'- and 3'-termini that can be functionalized further or used to incorporate the catenane structure into other DNA assemblies.

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

  • Anthracenes / chemical synthesis*
  • Anthracenes / chemistry*
  • Anthracenes / radiation effects
  • DNA / chemistry*
  • DNA / radiation effects
  • Molecular Structure
  • Nucleic Acid Conformation
  • Oligonucleotides / chemistry
  • Oligonucleotides / radiation effects
  • Stereoisomerism
  • Ultraviolet Rays

Substances

  • Anthracenes
  • Oligonucleotides
  • catenane
  • DNA