Far UV synchrotron radiation circular dichroism of guanine nucleosides

Synchrotron radiation circular dichroism spectra of 2'-deoxyribonucleosides, as well as a few guanine nucleosides were recorded between 170-330 nm. The CD profile of each nucleoside is unique, and there is a general similarity in the SRCD patterns of deoxyribonucleosides and those recorded by a benchtop CD as previously reported. Furthermore, the locked nucleic acid derivative of guanine nucleoside (LNA-G) showed opposite CD profiles to the rest of the guanine nucleoside derivatives. The conformational parameters of the nucleosides were analyzed against the crystal structures available in the Cambridge Crystallographic Data Center. The pseudorotational phase angles of the guanine nucleoside derivatives in solution were also determined based on NMR coupling constants. Analyses showed no apparent correlation between pseudorotational phase angles and CD patterns.

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Publication Details

Journal
Nucleosides Nucleotides & Nucleic Acids
Published
2025-11-07
DOI
https://doi.org/10.1080/15257770.2025.2585120
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
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article

Far UV synchrotron radiation circular dichroism of guanine nucleosides

Hongbin Yan, Frank Wien, Thad A. Harroun, Jesse Vanloon et al.
Nucleosides Nucleotides & Nucleic Acids
DNA and Nucleic Acid Chemistry
article

Far UV synchrotron radiation circular dichroism of guanine nucleosides

Hongbin Yan, Frank Wien, Thad A. Harroun, Jesse Vanloon, Mariam El‐Morched, J.D. King
article en

Abstract

Synchrotron radiation circular dichroism spectra of 2'-deoxyribonucleosides, as well as a few guanine nucleosides were recorded between 170-330 nm. The CD profile of each nucleoside is unique, and there is a general similarity in the SRCD patterns of deoxyribonucleosides and those recorded by a benchtop CD as previously reported. Furthermore, the locked nucleic acid derivative of guanine nucleoside (LNA-G) showed opposite CD profiles to the rest of the guanine nucleoside derivatives. The conformational parameters of the nucleosides were analyzed against the crystal structures available in the Cambridge Crystallographic Data Center. The pseudorotational phase angles of the guanine nucleoside derivatives in solution were also determined based on NMR coupling constants. Analyses showed no apparent correlation between pseudorotational phase angles and CD patterns.

Nucleosides Nucleotides & Nucleic Acids
Brock University (CA), Synchrotron soleil (FR)
Openalex Percentile: Top 70%
DNA and Nucleic Acid Chemistry
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