Related Experiment Video
Updated: May 24, 2026

03:38
Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction
Published on: October 6, 2022
G-quadruplex based probes for visual detection and sensing
J L Neo1, K Kamaladasan, M Uttamchandani
1Defence Medical and Environmental Research Institute, DSO National Laboratories, Singapore, Republic of Singapore.
Current Pharmaceutical Design
|March 3, 2012
Summary
G-quadruplex-hemin DNAzymes offer rapid, on-site detection by mimicking enzymes. This review explores their use in colorimetric biosensing for diverse targets like nucleic acids and metal ions.
Area of Science:
- Biotechnology and Biosensing
- Molecular Biology
- Analytical Chemistry
Background:
- Colorimetric biosensing enables rapid, on-site detection methods.
- G-quadruplex-hemin DNAzymes possess peroxidase-like activity.
- These DNAzymes are synthesized from G-rich DNA sequences.
Purpose of the Study:
- To review strategies for using G-quadruplex-hemin DNAzymes in optical biosensing.
- To highlight their application in detecting various chemical and biological targets.
Main Methods:
- Exploiting the peroxidase-like catalytic activity of G-quadruplex-hemin DNAzymes.
- Utilizing the oxidation of substrate precursors into colored products for detection.
- Leveraging modular G-rich DNA sequences for probe synthesis.
Main Results:
- Demonstrated versatility of DNAzymes for detecting nucleic acids, proteins, and metal ions.
- Established DNAzymes as efficient probes for colorimetric detection.
- Showcased cost-effective and convenient synthesis of DNAzyme probes.
Conclusions:
- G-quadruplex-hemin DNAzymes are powerful tools for optical biosensing.
- Their modular nature and catalytic activity facilitate diverse target detection.
- These DNAzymes hold significant potential for point-of-need applications.
Related Concept Videos
Labeling DNA Probes
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
In-situ Hybridization
In situ hybridization (ISH) is a technique used to detect and localize specific DNA or RNA molecules in cells, tissue, or tissue sections using a labeled probe. The technique was first used in 1969 for the investigation of nucleic acids. It is currently an essential tool in scientific research and clinical settings, especially for diagnostic purposes.
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...

