A convenient synthesis of DNA fragments nitrogen‐15 labeled at the exocyclic cytosine amino group

E. R. Kellenbach, H. van den Elst, R. Boelens, G. A. van der Marel, J. H. van Boom, R. Kaptein*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A convenient method is described for the synthesis of oligodeoxynucleotides 15N labeled at the exocyclic amino group of cytosine. The 4‐triazolide derivative of deoxyuridine is used as a building block in the solid phase synthesis of the oligodeoxynucleotide. Deprotection and cleavage from the solid support is achieved by treatment with 15N labeled NH4OH. This treatment also substitutes the 4‐triazolide group of the deoxyuridine by an 15N labeled amino group to yield 4‐15N cytosine. The method was applied to a DNA fragment corresponding to a glucocorticoid response element. The oligomer was characterised by 1H‐15N coherence spectroscopy.

Original languageEnglish
Pages (from-to)387-388
Number of pages2
JournalRecueil des Travaux Chimiques des Pays‐Bas
Volume110
Issue number9
DOIs
Publication statusPublished - 1991

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