Rapid and efficient DNA strand cross-linking by click chemistry

Chembiochem. 2008 May 23;9(8):1280-5. doi: 10.1002/cbic.200800006.

Abstract

Click chemistry has been used to covalently cross-link complementary DNA strands between bases to form very stable duplexes. Several alkyne- and azide-modified uracil monomers were used to evaluate the effect of the linkers on the efficiency of the click reaction. All cross-linked duplexes had much higher thermal stabilities than non-cross-linked ones, with increases in melting temperature of up to 30 degrees C. In some cases, the conversion was near-quantitative, and the reaction was complete in 5 min.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry
  • Azides / chemistry
  • Circular Dichroism
  • Cross-Linking Reagents / chemistry*
  • DNA / chemistry*
  • Deoxyuridine / chemistry
  • Electrophoresis, Capillary
  • Molecular Structure
  • Oligonucleotides / chemical synthesis
  • Oligonucleotides / chemistry
  • Time Factors

Substances

  • Alkynes
  • Azides
  • Cross-Linking Reagents
  • Oligonucleotides
  • DNA
  • Deoxyuridine