This article is cited in 42 papers

Modern methods for the synthesis of peptide–oligonucleotide conjugates

E. M. Zubin^a, E. A. Romanova^b, T. S. Oretskaya<sup>a

a</sup> Lomonosov Moscow State University, Faculty of Chemistry
^b Lomonosov Moscow State University, Belozersky Research Institute of Physico-Chemical Biology

Abstract: The published data on the methods of chemical solution and solid-phase synthesis of peptide–oligonucleotide conjugates are reviewed. The known methods are systematised and their advantages and disadvantages are considered. The approaches to the solution synthesis of peptide–oligonucleotide conjugates are systematised according to the type of chemical bonds between the fragments, whereas those to the solid-phase synthesis are classified according to the procedure used for the preparation of conjugates, viz., stepwise elongation of oligonucleotide and peptide chains on the same polymeric support or solid-phase condensation of two presynthesised fragments. The bibliography includes 141 references.

Received: 13.12.2001

DOI: 10.1070/RC2002v071n03ABEH000707

 English version: Russian Chemical Reviews, 2002, 71:3, 239–264

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