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Detection of Multiplex NASBA RNA Products Using Colorimetric Split G Quadruplex Probes
Maria S Rubel1, Liubov A Shkodenko2, Daria A Gorbenko2
1Laboratory of DNA-Nanosensor Diagnostics, ITMO University, Saint Petersburg, Russia. rubel@scamt-itmo.ru.
Methods in Molecular Biology (Clifton, N.J.)
|August 12, 2023
Summary
This study presents G-quadruplex DNA sensors for detecting RNA amplicons. These sensors provide a colorimetric signal, simplifying the recognition of challenging structural RNA targets.
Area of Science:
- Molecular Biology
- Biochemistry
- Analytical Chemistry
Background:
- Structural RNA poses significant challenges for detection using conventional hybridization probes.
- Multiplex nucleic acid sequence-based amplification (NASBA) generates RNA amplicons that require robust recognition methods.
Purpose of the Study:
- To address the difficulty of recognizing structural RNA amplicons from multiplex NASBA.
- To develop a novel sensor system for sensitive and specific detection of RNA targets.
Main Methods:
- Design and implementation of G-quadruplex binary (split) DNA peroxidase sensors.
- Utilizing the G-quadruplex structure for specific recognition of target RNA amplicons.
- Generating a colorimetric signal indicative of successful amplicon recognition.
Main Results:
- Demonstrated the successful design of G-quadruplex binary DNA sensors.
- Showcased the sensor's ability to produce a colorimetric signal upon binding NASBA amplicons.
- Validated the sensor's effectiveness in recognizing challenging structural RNA targets.
Conclusions:
- G-quadruplex binary DNA sensors offer a viable solution for detecting structural RNA amplicons.
- The developed colorimetric method enhances the recognition of RNA targets in complex samples.
- This approach advances nucleic acid detection technologies for molecular diagnostics.
Keywords:
Folded RNANucleic acid sequence-based amplification (NASBA)Peroxidase-based DNAzymeSplit (binary) probesVisual detection
