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A competitive aptamer binding-based CRISPR-cas biosensor for sensitive detection of tetracycline residues in
Yali Zhang1, Xingpeng Dong2, Cuijuan Jiang3
1Key Laboratory of Inflammation and Molecular Drug Targets of Jiangsu Province, School of Medicine, School of Pharmacy, Nantong University, Nantong 226001, China.
Abstract:
Tetracycline (TC) is widely used in veterinary medicine and animal feed; however, TC residues in food pose a risk to human health. Thus, the sensitive and selective detection of TC is needed to ensure food safety. Herein, we developed a CRISPR-Cas12a biosensor with competitive aptamer binding to detect TC residues. The aptasensor, formed by hybridizing activator DNA with TC-specific aptamers on streptavidin-modified magnetic beads, releases activator DNA in a TC concentration-dependent manner. This activated the Cas12a-crRNA complex, which cleaved single-strand DNA reporters to generate a detectable fluorescence signal. The TC signal was amplified through a two-step incubation reaction, with a detection limit as low as 9.45 × 10-5 μg L-1. The assay showed high selectivity and good recovery rates in various biological samples (e.g., honey, milk, fish), demonstrating the applicability of the biosensors in pollutant detection.
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