UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

DNA-binding properties of new fluorescent AzaHx-amides: Methoxy-pyridyl-aza-benzimidazole-pyrrole-imidazole/pyrrole

Liu, B; Pett, L; Kiakos, K; Patil, PC; Satam, V; Hartley, JA; Lee, M; (2018) DNA-binding properties of new fluorescent AzaHx-amides: Methoxy-pyridyl-aza-benzimidazole-pyrrole-imidazole/pyrrole. ChemBioChem , 19 (18) pp. 1979-1987. 10.1002/cbic.201800273. Green open access

[thumbnail of Liu_et_al-2018-ChemBioChem.pdf]
Preview
Text
Liu_et_al-2018-ChemBioChem.pdf - Accepted Version

Download (1MB) | Preview

Abstract

DNA minor groove binding polyamides have been extensively developed to control abnormal gene expression. Establishment of the novel, inherently fluorescent Hx-amides has provided an alternative path for studying DNA binding in cells by direct observation of cell localization. Because of the 2:1 antiparallel stacking homodimer binding mode of these molecules to DNA, modification of Hx-amides to AzaHx-amides has successfully extended the DNA recognition repertoire, from central CG (recognized by Hx-I) to central GC (recognized by AzaHx-P) recognition. To potentially target two consecutive GG bases, new modifications from AzaHx moiety to 3-Pyr-AzaHx and 2-Pyr-AzaHx moieties were developed. The newly designed molecules are also small-sized, fluorescent amides with Pyr-AzaHx connected to two conventional five-membered heterocycles. Complementary biophysical methods were carried out to investigate DNA binding properties of these molecules. The results showed that neither 3-Pyr-AzaHx nor 2-Pyr-AzaHx was able to mimic I-I to specifically target GG dinucleotides. Rather, 3-Pyr-AzaHx functions like AzaHx or f-I or P-I as a antiparallel stacked dimer. 3-Pyr-AzaHx-PI (2) binds 5'-ACGCGT'-3' with improved binding affinity and high sequence specificity when compared to its parent molecule AzaHx-PI (1). However, 2-Pyr-AzaHx is detrimental to DNA binding because of an unfavorable steric clash upon stacking in the minor groove.

Type: Article
Title: DNA-binding properties of new fluorescent AzaHx-amides: Methoxy-pyridyl-aza-benzimidazole-pyrrole-imidazole/pyrrole
Location: Germany
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/cbic.201800273
Publisher version: https://doi.org/10.1002/cbic.201800273
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: 3-Pyr-AzaHx, AzaHx, DNA recognition, fluorescent, polyamides
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute > Research Department of Oncology
URI: https://discovery.ucl.ac.uk/id/eprint/10054031
Downloads since deposit
83Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item