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Updated: Mar 9, 2026

Aptamer-Based Target Detection Facilitated by a 3-Stage G-Quadruplex Isothermal Exponential Amplification Reaction
Published on: October 6, 2022
A graphene oxide-based strand displacement amplification platform for ricin detection using aptamer as recognition
Chun Hong Li1, Xue Xiao1, Jing Tao1
1Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, 400715 Chongqing, PR China.
A new method detects ricin toxin B-chain (RTB) using aptamers and graphene oxide. This sensitive isothermal strand-displacement polymerase reaction (ISDPR) offers a rapid detection strategy for bioterrorism threats.
Area of Science:
- Biochemistry
- Analytical Chemistry
- Biotechnology
Background:
- Ricin is a toxic plant protein posing a significant bioterrorism threat due to its accessibility.
- Effective detection methods are crucial for mitigating ricin-related risks.
Purpose of the Study:
- To develop a novel, sensitive, and rapid detection strategy for ricin B-chain (RTB).
- To utilize aptamers and graphene oxide for enhanced detection performance.
Main Methods:
- Isothermal strand-displacement polymerase reaction (ISDPR) coupled with aptamer recognition.
- Graphene oxide (GO) employed as a low-background platform for signal amplification.
- Detection based on fluorescence signal changes triggered by RTB binding.
Main Results:
- The developed system achieved a linear detection range from 0.75μg/mL to 100μg/mL.
- A low limit of detection (3σ) of 0.6μg/mL for RTB was established.
- Successful detection of RTB and whole ricin toxin in real samples was demonstrated.
Conclusions:
- The novel ISDPR method provides a sensitive and reliable approach for ricin detection.
- The strategy is adaptable for detecting various targets by employing specific aptamers.
- This offers a promising tool for bioterrorism surveillance and diagnostics.
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