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Updated: Jan 31, 2026

A Method for Selecting Structure-switching Aptamers Applied to a Colorimetric Gold Nanoparticle Assay
Published on: February 28, 2015
Low-Micromolar-Pressure Capture-SELEX Yields Fold-Switching DNA Aptamers for Label-Free Quantification of
Weijuan Yang1, Yufan Xiao1, Lili An1
1Key Laboratory of Biopesticide and Chemical Biology of MOE, College of Bee Science and Biomedicine, Fujian Agriculture and Forestry University, Fuzhou, Fujian 350002, China.
Abstract:
Benzovindiflupyr (BZF) is a widely used succinate dehydrogenase inhibitor whose persistence complicates monitoring in food and environmental matrices. We implemented a capture-SELEX campaign that constrained ligand concentrations from low micromolar to submicromolar across 13 rounds, creating a low-pressure evolutionary bottleneck. This approach yielded two high-affinity aptamers: Apt.BZF01 (KD = 67.0 ± 9.7 nM) forming a parallel G-quadruplex and Apt.BZF02 (KD = 25.8 ± 5.8 nM) exhibiting ligand-induced fold-switching. Both aptamers showed no cross-reactivity against 21 pesticides. Leveraging Apt.BZF02's conformational switching, we developed a label-free Thioflavin T displacement assay achieving 17 nM detection limit that maintains performance in complex matrices, with 93-104% recoveries in grape homogenate. This study provides a sensitive detection platform and offers a generalizable blueprint for coupling low-target-pressure SELEX with fold-switch-enabled readouts for challenging hydrophobic targets.
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