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. 1996 Aug 1;24(15):3048–3052. doi: 10.1093/nar/24.15.3048

Acid binding and detritylation during oligonucleotide synthesis.

C H Paul 1, A T Royappa 1
PMCID: PMC146054  PMID: 8760892

Abstract

Under the conditions normally used for detritylation in oligonucleotide synthesis, the haloacetic acid binds strongly to the oligonucleotide. Acetonitrile also forms a complex with the deblocking acid, in competition with the oligonucleotide, and drastically slows detritylation. Incomplete removal of acetonitrile during the deblock step may slow the kinetics enough to result in incomplete detritylation of the oligonucleotide. Acid binding to the growing oligonucleotide causes striking chromatographic effects in the presence of high oligonucleotide mass densities. In packed-bed column reactors, at low linear velocities, the acid binding almost completely depletes free acid from the deblocking solution. This results in an advancing zone within which the oligonucleotide is saturated with acid. Detritylation occurs mostly in a narrow band at the front of the advancing saturated zone. Increasing the DCA concentration in order to achieve quick saturation can give faster and more complete detritylation while minimizing the exposure time of the oligonucleotide to acid.

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Selected References

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

  1. Fearon K. L., Stults J. T., Bergot B. J., Christensen L. M., Raible A. M. Investigation of the 'n-1' impurity in phosphorothioate oligodeoxynucleotides synthesized by the solid-phase beta-cyanoethyl phosphoramidite method using stepwise sulfurization. Nucleic Acids Res. 1995 Jul 25;23(14):2754–2761. doi: 10.1093/nar/23.14.2754. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Septak M. Kinetic studies on depurination and detritylation of CPG-bound intermediates during oligonucleotide synthesis. Nucleic Acids Res. 1996 Aug 1;24(15):3053–3058. doi: 10.1093/nar/24.15.3053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Temsamani J., Kubert M., Agrawal S. Sequence identity of the n-1 product of a synthetic oligonucleotide. Nucleic Acids Res. 1995 Jun 11;23(11):1841–1844. doi: 10.1093/nar/23.11.1841. [DOI] [PMC free article] [PubMed] [Google Scholar]

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