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Updated: Jan 25, 2026

05:37
Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
Published on: April 4, 2025
1.2K
Light-controlled thrombin catalysis and clot formation using a photoswitchable G-quadruplex DNA aptamer
Aysha Ali1, Gemma A Bullen, Benjamin Cross
1School of Chemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK. j.tucker@bham.ac.uk.
Summary
Researchers demonstrate reversible photocontrol of blood coagulation using a modified thrombin binding aptamer (TBA). Light triggers structural changes, inhibiting thrombin and controlling clotting.
Area of Science:
- Biochemistry
- Molecular Biology
- Biotechnology
Background:
- Blood coagulation is a complex process involving enzymes like thrombin.
- Controlling coagulation is crucial for treating bleeding disorders and thrombosis.
- Existing methods for coagulation control can be invasive or lack precise temporal regulation.
Purpose of the Study:
- To develop a light-controllable system for regulating blood coagulation.
- To demonstrate reversible photocontrol of thrombin activity using a modified aptamer.
Main Methods:
- Modification of thrombin binding aptamer (TBA) with two anthracene groups to render it photochromic.
- Induction of anthracene photodimerization using light to alter TBA structure.
- Assessment of the effect of light-induced structural changes on thrombin binding and subsequent coagulation activity.
Main Results:
- Light-triggered photodimerization of anthracene groups caused structural distortion of the TBA.
- The distorted TBA exhibited inhibited binding to thrombin.
- This inhibition of thrombin binding reversibly controlled the blood clotting process.
Conclusions:
- Reversible photocontrol of blood coagulation is achievable through light-modulated aptamer structure.
- Photochromic aptamers offer a novel, non-invasive strategy for regulating enzyme activity.
- This approach has potential applications in hemostasis and thrombosis management.
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