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Mapping the Binding Site of an Aptamer on ATP Using MicroScale Thermophoresis
Published on: January 7, 2017
Using azobenzene incorporated DNA aptamers to probe molecular binding interactions
Joseph A Phillips1, Haipeng Liu, Meghan B O'Donoghue
1Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, United States.
Bioconjugate Chemistry
|January 21, 2011
Summary
Researchers developed novel DNA/RNA aptamer probes with two structural states using azobenzene. This allows for studying target-aptamer interactions by analyzing binding affinity changes, enabling new therapeutic applications.
Area of Science:
- Biochemistry
- Molecular Biology
- Biotechnology
Background:
- Rational design of DNA/RNA aptamers as molecular probes requires understanding structure-function relationships.
- Aptamer-target binding is influenced by aptamer structural conformation.
Purpose of the Study:
- To present a method for creating aptamer probes capable of adopting two distinct structural states.
- To elucidate target-aptamer binding interactions by analyzing differences in binding affinity between these states.
Main Methods:
- Incorporation of azobenzene into DNA strands to photoregulate DNA duplex melting.
- Utilizing light-regulated conformational changes of azobenzene in aptamers to analyze secondary structure's role in target binding.
Main Results:
- Azobenzene-modified aptamers maintained target selectivity.
- Binding affinity varied based on the number, position, and conformation of azobenzene modifications.
Conclusions:
- Aptamer probes can be designed to switch binding affinity on demand.
- This controllable binding affinity has potential applications in targeted drug delivery and photodynamic therapy.
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