Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1997 Dec 15;25(24):5127–5129. doi: 10.1093/nar/25.24.5127

Microwave-assisted rapid deprotection of oligodeoxyribonucleotides.

P Kumar 1, K C Gupta 1
PMCID: PMC147135  PMID: 9396826

Abstract

A novel method for the deprotection of oligodeoxyribonucleotides under microwave irradiation has been developed. The oligodeoxynucleotides having base labile, phenoxyacetyl (pac), protection for exocyclic amino functions were fully deprotected in 0. 2 M sodium hydroxide (methanol:water : : 1:1, v/v) = A and 1 M sodium hydroxide (methanol:water : : 1:1, v/v) = B using microwaves in 4 and 2 min, respectively. The deprotection of oligodeoxyribonucleotides carrying conventional protecting groups, dAbz, dCbzand dGpac, for exocyclic amino functions was achieved in 4 min in B without any side product formation. The deprotected oligonucleotides were compared with the oligomers deprotected using standard deprotection conditions (29% aq. ammonia, 16 h, 55 degrees C) with respect to their retention time on HPLC and biological activity.

Full Text

The Full Text of this article is available as a PDF (56.9 KB).

Selected References

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

  1. Boal J. H., Wilk A., Harindranath N., Max E. E., Kempe T., Beaucage S. L. Cleavage of oligodeoxyribonucleotides from controlled-pore glass supports and their rapid deprotection by gaseous amines. Nucleic Acids Res. 1996 Aug 1;24(15):3115–3117. doi: 10.1093/nar/24.15.3115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Pon R. T., Buck G. A., Niece R. L., Robertson M., Smith A. J., Spicer E. A survey of nucleic acid services in core laboratories. Biotechniques. 1994 Sep;17(3):526–534. [PubMed] [Google Scholar]
  3. Schulhof J. C., Molko D., Teoule R. Synthesis of DNA fragments containing 5,6-dihydrothymine, a major product of thymine gamma radiolysis. Nucleic Acids Res. 1988 Jan 11;16(1):319–326. doi: 10.1093/nar/16.1.319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Sinha N. D., Davis P., Usman N., Pérez J., Hodge R., Kremsky J., Casale R. Labile exocyclic amine protection of nucleosides in DNA, RNA and oligonucleotide analog synthesis facilitating N-deacylation, minimizing depurination and chain degradation. Biochimie. 1993;75(1-2):13–23. doi: 10.1016/0300-9084(93)90019-o. [DOI] [PubMed] [Google Scholar]

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

RESOURCES