Spectroscopic, biochemical and computational studies of bioactive DNA minor groove binders targeting 5′-WGWWCW-3′ motif

Alniss, Hasan Y. and Kemp, Bryony M. and Holmes, Elizabeth and Hoffman, Joanna and Ploch, Rafal M. and Ramadan, Wafaa S. and Msallam, Yousef A. and Al-Jubeh, Hadeel M. and Madkour, Moustafa M. and Celikkaya, Bekir Caglar and Scott, Fraser J. and El-Awady, Raafat and Parkinson, John A. (2024) Spectroscopic, biochemical and computational studies of bioactive DNA minor groove binders targeting 5′-WGWWCW-3′ motif. Bioorganic Chemistry, 148. 107414. ISSN 1090-2120 (https://doi.org/10.1016/j.bioorg.2024.107414)

[thumbnail of Alniss-etal-BC-2024-Spectroscopic-biochemical-and-computational-studies-of-bioactive-DNA]
Preview
Text. Filename: Alniss-etal-BC-2024-Spectroscopic-biochemical-and-computational-studies-of-bioactive-DNA.pdf
Accepted Author Manuscript
License: Creative Commons Attribution 4.0 logo

Download (4MB)| Preview

Abstract

Spectroscopic, biochemical, and computational modelling studies have been used to assess the binding capability of a set of minor groove binding (MGB) ligands against the self complementary DNA sequences 5’-d(CGCACTAGTGCG)-3’ and 5’-d(CGCAGTACTGCG)-3’. The ligands were carefully designed to target the DNA response element, 5′-WGWWCW-3′, the binding site for several nuclear receptors. Basic 1D 1H NMR spectra of the DNA samples prepared with three MGB ligands show subtle variations suggestive of how each ligand associates with the double helical structure of both DNA sequences. The variations among the investigated ligands were reflected in the line shape and intensity of 1D 1H and 31P-{1H} NMR spectra. Rapid visual inspection of these 1D NMR spectra proves to be beneficial in providing valuable insights on MGB binding molecules. The NMR results were consistent with the findings from both UV DNA denaturation and molecular modelling studies. Both the NMR spectroscopic and computational analyses indicate that the investigated ligands bind to the minor grooves as antiparallel side-by-side dimers in a head-to-tail fashion. Moreover, comparisons with results from biochemical studies offered valuable insights into the mechanism of action, and antitumor activity of MGBs in relation to their structures, essential pre-requisites for future optimization of MGBs as therapeutic agents.

ORCID iDs

Alniss, Hasan Y., Kemp, Bryony M., Holmes, Elizabeth, Hoffman, Joanna, Ploch, Rafal M., Ramadan, Wafaa S., Msallam, Yousef A., Al-Jubeh, Hadeel M., Madkour, Moustafa M., Celikkaya, Bekir Caglar ORCID logoORCID: https://orcid.org/0000-0002-8677-9101, Scott, Fraser J. ORCID logoORCID: https://orcid.org/0000-0003-0229-3698, El-Awady, Raafat and Parkinson, John A. ORCID logoORCID: https://orcid.org/0000-0003-4270-6135;