Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1997 Oct 15;25(20):3980–3983. doi: 10.1093/nar/25.20.3980

RNA synthesis using a universal, base-stable allyl linker.

X Zhang 1, B L Gaffney 1, R A Jones 1
PMCID: PMC147002  PMID: 9321646

Abstract

The application of a universal allyl linker, 9-O-(4,4'-dimethoxytrityl)-10-undecenoic acid, to the solid phase synthesis of RNA molecules is described. Use of this linker simplifies significantly the isolation and purification steps in RNA synthesis. The linker is universal in that it does not contain a nucleoside. The 3'terminal nucleoside is instead attached to the support in the first coupling step. The resultant RNA fragment is then obtained as the 3'-phosphate. The linker is base-stable, and thus all reagents used during deprotection can simply be washed away, leaving the RNA attached. Further, tritylated short fragments resulting from chain cleavage for any reason are also washed away before separation from the support. This linker is compatible with any current synthetic methodology and any amino functionalized support. Of course, silica supports would not be compatible with fluoride reagents. It could also be used to advantage for other applications. Because it is cleaved under conditions orthogonal to those used during many common reactions, the range of post-synthetic manipulations that can be carried out without cleavage from the support is extended significantly.

Full Text

The Full Text of this article is available as a PDF (55.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Gasparutto D., Livache T., Bazin H., Duplaa A. M., Guy A., Khorlin A., Molko D., Roget A., Téoule R. Chemical synthesis of a biologically active natural tRNA with its minor bases. Nucleic Acids Res. 1992 Oct 11;20(19):5159–5166. doi: 10.1093/nar/20.19.5159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Horn T., Urdea M. S. Solid supported hydrolysis of apurinic sites in synthetic oligonucleotides for rapid and efficient purification on reverse-phase cartridges. Nucleic Acids Res. 1988 Dec 23;16(24):11559–11571. doi: 10.1093/nar/16.24.11559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Lyttle M. H., Hudson D., Cook R. M. A new universal linker for solid phase DNA synthesis. Nucleic Acids Res. 1996 Jul 15;24(14):2793–2798. doi: 10.1093/nar/24.14.2793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Matray T. J., Yoo D. J., McMinn D. L., Greenberg M. M. Synthesis of oligonucleotides containing 3'-alkylcarboxylic acids using a palladium labile oligonucleotide solid phase synthesis support. Bioconjug Chem. 1997 Mar-Apr;8(2):99–102. doi: 10.1021/bc970013a. [DOI] [PubMed] [Google Scholar]
  5. Westman E., Strömberg R. Removal of t-butyldimethylsilyl protection in RNA-synthesis. Triethylamine trihydrofluoride (TEA, 3HF) is a more reliable alternative to tetrabutylammonium fluoride (TBAF). Nucleic Acids Res. 1994 Jun 25;22(12):2430–2431. doi: 10.1093/nar/22.12.2430. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Wincott F., DiRenzo A., Shaffer C., Grimm S., Tracz D., Workman C., Sweedler D., Gonzalez C., Scaringe S., Usman N. Synthesis, deprotection, analysis and purification of RNA and ribozymes. Nucleic Acids Res. 1995 Jul 25;23(14):2677–2684. doi: 10.1093/nar/23.14.2677. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES