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Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Amino-Functionalized Oligonucleotides with Peptide Internucleotide Linkages

Author(s): Anna M. Varizhuk, Svetlana V. Kochetkova, Alexander U. Fedotov, Natalia A. Kolganova, Edward N. Timofeev and Vladimir L. Florentiev

Volume 9, Issue 2, 2012

Page: [106 - 113] Pages: 8

DOI: 10.2174/157017812800221799

Price: $65

Abstract

Oligonucleotide analogs with L- and D-lysine residues incorporated in internucleotide linkages were synthesized and their affinity toward complementary DNA was studied. Stability of the duplexes formed by the modified oligonucleotides and their wild-type complements appeared to be close to that of the isosequential unmodified duplex, oligonucleotides carrying D-lysine residues forming generally more stable duplexes than L-lysine derivatives.

Keywords: Analogs, hybridization, oligonucleotides, peptide internucleotide linkages, synthesis, thermal stability, duplexes, triplexes, epimerization, dichloromethane


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