Citation

  • Authors: Voirin, E., Behr, J. P., Kotera, M.
  • Year: 2007
  • Journal: Nat Protoc 2 1360-7
  • Applications: in vitro / Zip Nucleic Acid® (ZNA®) / None
  • Cell type: None

Method

ZNA (Zip Nucleic Acids)

Abstract

A protocol for the rapid, automated synthesis of oligospermine-oligonucleotide sequences is described. To this end, a protected spermine phosphoramidite derivative was synthesized in six steps from spermine and used as the fifth synthon in an oligonucleotide synthesizer. Parameters were optimized to reach greater than 95% coupling yields. Cationic oligonucleotides show enhanced hybridization and strand invasion properties, and hence are an alternative to conventional oligonucleotides for molecular biology, diagnostic and potential therapeutic applications. A multi-gram-scale synthesis of the spermine phosphoramidite allowing several hundred coupling steps takes 2-3 weeks. Oligonucleotide synthesis and purification takes approximately 3 d.

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