Lumos: A <i>β</i>‐Diketone‐Derived Artificial Nucleobase Forming Inter‐Strand Complexes in DNA that Promote Lanthanoid Ion Luminescence

Abstract A novel artificial nucleobase, 1‐(3‐(hydroxymethyl)phenyl)‐3‐phenylpropane‐1,3‐dione (Hdbm OR ), containing a β ‐diketone designed to form inter‐strand complexes that resemble metal‐mediated base pairs, was synthesized and characterized towards its lanthanoid ion binding properties. Based on UV/vis spectra, a (labile) coordination of Eu III and Sm III by the benzyl‐functionalized model ligand is proposed, allowing the detection of distinct luminescence patterns upon coordination under alkaline conditions. The compatibility of the nucleoside analog with automated solid‐phase DNA synthesis was proven by the generation of a dinucleotide. NMR spectroscopic characterization of this dinucleotide revealed a temperature‐dependent equilibrium of two conformers, which likely involve hydrogen bonding of the β ‐diketone moiety and the deoxyribose and/or phosphate moieties. The antenna effect of the new ligand promoting the luminescence of Eu III is retained upon incorporation into DNA. Modification of a parallel‐stranded DNA duplex with a terminal homo base pair of Hdbm OR allows, despite natural fraying of DNA, a thermal stabilization of about 3 °C upon coordination of Eu III or Sm III . Temperature‐dependent luminescence spectroscopy demonstrates a direct correlation between the thermal stability of the duplex and its luminescence intensity. The ligand extends the library of artificial nucleobases for lanthanoid‐mediated base pairs, combining the luminescence properties of lanthanoid complexes with the self‐assembly properties of DNA.

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Publication Details

Journal
ChemistryEurope
Published
2025-02-03
DOI
https://doi.org/10.1002/ceur.202400116
Citations
3
Primary Topic
Lanthanide and Transition Metal Complexes
Type
article
Field-Weighted Citation Impact
1.55
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article

Lumos: A β‐Diketone‐Derived Artificial Nucleobase Forming Inter‐Strand Complexes in DNA that Promote Lanthanoid Ion Luminescence

Jens Müller, Marian Hebenbrock, Alexander Hepp, Carla Bardehle
3 citations
ChemistryEurope
Lanthanide and Transition Metal Complexes
1.55
article

Lumos: A β‐Diketone‐Derived Artificial Nucleobase Forming Inter‐Strand Complexes in DNA that Promote Lanthanoid Ion Luminescence

Jens Müller, Marian Hebenbrock, Alexander Hepp, Carla Bardehle
article en
3 citations

Abstract

Abstract A novel artificial nucleobase, 1‐(3‐(hydroxymethyl)phenyl)‐3‐phenylpropane‐1,3‐dione (Hdbm OR ), containing a β ‐diketone designed to form inter‐strand complexes that resemble metal‐mediated base pairs, was synthesized and characterized towards its lanthanoid ion binding properties. Based on UV/vis spectra, a (labile) coordination of Eu III and Sm III by the benzyl‐functionalized model ligand is proposed, allowing the detection of distinct luminescence patterns upon coordination under alkaline conditions. The compatibility of the nucleoside analog with automated solid‐phase DNA synthesis was proven by the generation of a dinucleotide. NMR spectroscopic characterization of this dinucleotide revealed a temperature‐dependent equilibrium of two conformers, which likely involve hydrogen bonding of the β ‐diketone moiety and the deoxyribose and/or phosphate moieties. The antenna effect of the new ligand promoting the luminescence of Eu III is retained upon incorporation into DNA. Modification of a parallel‐stranded DNA duplex with a terminal homo base pair of Hdbm OR allows, despite natural fraying of DNA, a thermal stabilization of about 3 °C upon coordination of Eu III or Sm III . Temperature‐dependent luminescence spectroscopy demonstrates a direct correlation between the thermal stability of the duplex and its luminescence intensity. The ligand extends the library of artificial nucleobases for lanthanoid‐mediated base pairs, combining the luminescence properties of lanthanoid complexes with the self‐assembly properties of DNA.

ChemistryEuropeVol. 3(3)
University of Münster (DE)
Openalex Percentile: Top 20%
Lanthanide and Transition Metal Complexes
1.55
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