Solution structure of Z-form DNA bound to a curaxin ligand CBL0137

Z-DNA is known to be a left-handed alternative form of DNA and has important biological roles in cancer and other genetic diseases. In a recent study, we discovered CBL0137, a curaxin ligand, to enhance cancer immunotherapy by inducing Z-DNA formation and activating the Z-DNA-binding protein ZBP1. However, the structural information on binding complexes between Z-DNA and CBL0137 ligand has not reported to date. Here we present the first high-resolution structure of the complex between a Z-DNA and a curaxin ligand CBL0137. This compound is observed to interact with the Z-DNA through π-stacking and zig-zag localization. Furthermore, we directly observe the complex in living human cells using in-cell 19F NMR for the first time. This structural information provides a platform for the design of topology-specific Z-DNA-targeting compounds and is valuable for the development of new potent anticancer drugs.

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Publication Details

Journal
Nucleic Acids Research
Published
2026-01-29
DOI
https://doi.org/10.1093/nar/gkag104
Primary Topic
Cancer therapeutics and mechanisms
Type
article
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article

Solution structure of Z-form DNA bound to a curaxin ligand CBL0137

Yan Xu, Feifan Liu, Shiyu Wang
Nucleic Acids Research
Cancer therapeutics and mechanisms
article

Solution structure of Z-form DNA bound to a curaxin ligand CBL0137

Yan Xu, Feifan Liu, Shiyu Wang
article en

Abstract

Z-DNA is known to be a left-handed alternative form of DNA and has important biological roles in cancer and other genetic diseases. In a recent study, we discovered CBL0137, a curaxin ligand, to enhance cancer immunotherapy by inducing Z-DNA formation and activating the Z-DNA-binding protein ZBP1. However, the structural information on binding complexes between Z-DNA and CBL0137 ligand has not reported to date. Here we present the first high-resolution structure of the complex between a Z-DNA and a curaxin ligand CBL0137. This compound is observed to interact with the Z-DNA through π-stacking and zig-zag localization. Furthermore, we directly observe the complex in living human cells using in-cell 19F NMR for the first time. This structural information provides a platform for the design of topology-specific Z-DNA-targeting compounds and is valuable for the development of new potent anticancer drugs.

Nucleic Acids ResearchVol. 54(4)
University of Miyazaki (JP)
Good health and well-being
Openalex Percentile: Top 61%
Cancer therapeutics and mechanisms
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