Nucleic acid chemistry in the organic phase: from functionalized oligonucleotides to DNA side chain polymers

J Am Chem Soc. 2014 Oct 8;136(40):14255-62. doi: 10.1021/ja5080486. Epub 2014 Sep 29.

Abstract

DNA-incorporating hydrophobic moieties can be synthesized by either solid-phase or solution-phase coupling. On a solid support the DNA is protected, and hydrophobic units are usually attached employing phosphoramidite chemistry involving a DNA synthesizer. On the other hand, solution coupling in aqueous medium results in low yields due to the solvent incompatibility of DNA and hydrophobic compounds. Hence, the development of a general coupling method for producing amphiphilic DNA conjugates with high yield in solution remains a major challenge. Here, we report an organic-phase coupling strategy for nucleic acid modification and polymerization by introducing a hydrophobic DNA-surfactant complex as a reactive scaffold. A remarkable range of amphiphile-DNA structures (DNA-pyrene, DNA-triphenylphosphine, DNA-hydrocarbon, and DNA block copolymers) and a series of new brush-type DNA side-chain homopolymers with high DNA grafting density are produced efficiently. We believe that this method is an important breakthrough in developing a generalized approach to synthesizing functional DNA molecules for self-assembly and related technological applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA / chemistry*
  • DNA / genetics
  • Hydrophobic and Hydrophilic Interactions
  • Models, Molecular
  • Nucleic Acid Conformation
  • Oligonucleotides / chemistry*
  • Organic Chemicals / chemistry*
  • Polymerization
  • Surface-Active Agents / chemistry

Substances

  • Oligonucleotides
  • Organic Chemicals
  • Surface-Active Agents
  • DNA