Issue 59, 2017, Issue in Progress

Exploring the preferential interaction of quercetin with VEGF promoter G-quadruplex DNA and construction of a pH-dependent DNA-based logic gate

Abstract

G-Quadruplex DNA (G4–DNA) is one of the most important non-canonical nucleic acid structures. G4–DNA forming sequences are present in different crucial genomic regions and are abundant in promoter regions of several oncogenes. Therefore, G4–DNA is an important target for anticancer drugs and hence binding interactions between G4–DNA and small molecule ligands are of great importance. Since G4–DNA is a highly polymorphic structure, it is important to identify ligand molecules which preferentially target a particular quadruplex sequence in comparison to other quadruplexes. In the present study, different spectroscopic techniques have been used to explore the interaction of the dietary plant flavonoid quercetin (Que) with various G4–DNA structures (VEGF, c-MYC, c-KIT1, c-KIT2, h-TELO) along with double stranded (duplex) DNA. We found that Que shows preferential interaction with VEGF G4–DNA compared to other G4–DNA structures as well as duplex DNA. This identifies Que as an appropriate natural product based ligand for targeting VEGF G4–DNA. We also observed pH dependent interaction of Que with VEGF G4–DNA, based on which we have designed a complex Boolean logic gate exploiting Que as a sensing molecule.

Graphical abstract: Exploring the preferential interaction of quercetin with VEGF promoter G-quadruplex DNA and construction of a pH-dependent DNA-based logic gate

Supplementary files

Article information

Article type
Paper
Submitted
26 May 2017
Accepted
21 Jul 2017
First published
27 Jul 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 37230-37240

Exploring the preferential interaction of quercetin with VEGF promoter G-quadruplex DNA and construction of a pH-dependent DNA-based logic gate

S. Bhattacharjee, P. K. Sengupta and S. Bhowmik, RSC Adv., 2017, 7, 37230 DOI: 10.1039/C7RA05930B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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