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Taylor and Francis Group, Nucleosides, Nucleotides and Nucleic Acids, 8-9(26), p. 963-967

DOI: 10.1080/15257770701508216

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New developments in the synthesis of oligonucleotide-peptide conjugates

This paper is available in a repository.
This paper is available in a repository.

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Abstract

The stability of oligodeoxynucleotides to trifluoroacetic acid is studied. Pyrimidine oligonucleotides were stable in the conditions used for the removal of t-butyl groups. Oligonucleotide-3'-peptide conjugates carrying pyrimidine oligonucleotides are prepared stepwise using peptide-supports and Fmoc, t-butyl strategy. Using this strategy we have prepared an oligonucleotide-peptide conjugate containing as peptide the leucine-rich fragment of FOS, a transcription factor involved in many important cellular processes. This conjugate has a long peptide sequence with a large number of trifunctional amino acids.