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Published on: November 21, 2017
DNA-binding study of anthraquinone derivatives using chemometrics methods
M B Gholivand1, S Kashanian, H Peyman
1Faculty of Chemistry, Sensor and Biosensor Research Center (SBRC) & Nanoscience and Nanotechnology Research Center (NNRC), Razi University, Kermanshah, Iran. mbgholivand@yahoo.com
Two anthraquinones, quinizarin and danthron, interact with CT-DNA. Partially intercalative and hydrogen binding are the primary modes of interaction, confirmed by spectroscopic and viscosity studies.
Area of Science:
- Biophysical Chemistry
- Molecular Interactions
- DNA Binding Studies
Background:
- Anthraquinones are a class of organic compounds with diverse biological activities.
- Understanding the interaction of small molecules with DNA is crucial for drug development and molecular biology.
Purpose of the Study:
- To investigate the binding modes of quinizarin and danthron with CT-DNA.
- To determine the binding constants and analyze the influence of environmental factors on the interaction.
Main Methods:
- UV-vis absorption spectroscopy
- Circular dichroism (CD) spectroscopy
- Viscosity measurements
- Principal Component Analysis (PCA) and INDICES methods
- Nonlinear least-squares analysis using EQUISPEC software
Main Results:
- Partially intercalative and hydrogen binding were identified as the dominant binding modes.
- The binding behavior was confirmed to be dependent on ionic strength and pH.
- Interactions with both double-stranded (ds) and single-stranded (ss) DNA were studied.
Conclusions:
- Quinizarin and danthron exhibit specific binding interactions with CT-DNA.
- The findings provide insights into the molecular mechanisms of anthraquinone-DNA interactions.
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