Synthesis and Metal‐Ion Binding Properties of Duplexes Containing Thymine Analogs with 1,2‐Diamine Groups

Thymidine analogue with a 1,2-diamino side chain at the 3N position is synthesized and converted into an amidite unit for oligonucleotide synthesis. It is used for preparing oligonucleotides containing a 1,2-diamino side chain as X residue. Thermal denaturation studies are performed on a duplex containing an X-X pair in the presence and absence of metal ions. Among various metal ions used in this research, Cd(II), Co(II), Cu(II), Ni(II), and Zn(II) ions increased the duplex stability. The results prove the new strategy to design metallo-base pairs containing various metal ions.

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Publication Details

Journal
ChemBioChem
Published
2025-03-27
DOI
https://doi.org/10.1002/cbic.202500017
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
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article

Synthesis and Metal‐Ion Binding Properties of Duplexes Containing Thymine Analogs with 1,2‐Diamine Groups

Shoji Fujiwara, Takahiro Atsugi, Akira Ono, Jiro Kondo
ChemBioChem
DNA and Nucleic Acid Chemistry
article

Synthesis and Metal‐Ion Binding Properties of Duplexes Containing Thymine Analogs with 1,2‐Diamine Groups

Shoji Fujiwara, Takahiro Atsugi, Akira Ono, Jiro Kondo
article en

Abstract

Thymidine analogue with a 1,2-diamino side chain at the 3N position is synthesized and converted into an amidite unit for oligonucleotide synthesis. It is used for preparing oligonucleotides containing a 1,2-diamino side chain as X residue. Thermal denaturation studies are performed on a duplex containing an X-X pair in the presence and absence of metal ions. Among various metal ions used in this research, Cd(II), Co(II), Cu(II), Ni(II), and Zn(II) ions increased the duplex stability. The results prove the new strategy to design metallo-base pairs containing various metal ions.

ChemBioChemVol. 26(11)
Kanagawa University (JP), Sophia University (JP)
Openalex Percentile: Top 95%
DNA and Nucleic Acid Chemistry
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