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Monitoring DNA-Ligand Interactions in Living Human Cells Using NMR Spectroscopy

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KRAFČÍKOVÁ Michaela DŽATKO Šimon CARON C. GRANZHAN A. FIALA Radovan LOJA Tomáš TEULADE-FICHOU M.P. FESSL T. HANSEL-HERTSCH R. MERGNY J.L. FOLDYNOVA-TRANTIRKOVA S. TRANTÍREK Lukáš

Rok publikování 2019
Druh Článek v odborném periodiku
Časopis / Zdroj Journal of the American Chemical Society
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://pubs.acs.org/doi/pdf/10.1021/jacs.9b03031
Doi http://dx.doi.org/10.1021/jacs.9b03031
Klíčová slova MINOR-GROOVE; NUCLEIC-ACID; DRUG DESIGN; DISCOVERY; BINDERS
Popis Studies on DNA-ligand interactions in the cellular environment are problematic due to the lack of suitable biophysical tools. To address this need, we developed an in-cell NMR-based approach for monitoring DNA-ligand interactions inside the nuclei of living human cells. Our method relies on the acquisition of NMR data from cells electroporated with preformed DNA-ligand complexes. The impact of the intracellular environment on the integrity of the complexes is assessed based on in-cell NMR signals from unbound and ligand-bound forms of a given DNA target. This technique was tested on complexes of two model DNA fragments and four ligands, namely, a representative DNA minor-groove binder (netropsin) and ligands binding DNA base-pairing defects (naphthalenophanes). In the latter case, we demonstrate that two of the three in vitro-validated ligands retain their ability to form stable interactions with their model target DNA in cellulo, whereas the third one loses this ability due to off-target interactions with genomic DNA and cellular metabolites. Collectively, our data suggest that direct evaluation of the behavior of drug-like molecules in the intracellular environment provides important insights into the development of DNA-binding ligands with desirable biological activity and minimal side effects resulting from off-target binding.
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