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Employing a cluster transfer strategy in a hybridisation chain reaction-silver nanocluster hybrid sensor for nucleic acid detection.

Analytical methods : advancing methods and applications 2026 Vol.18(7) p. 1392-1396

New SY, Yoong Chan NJ, Ying Ooi JS

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The hybridisation chain reaction (HCR) is a robust isothermal amplification technique widely used for nucleic acid detection, often paired with silver nanoclusters (AgNCs) for fluorescence-based reado

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APA New SY, Yoong Chan NJ, Ying Ooi JS (2026). Employing a cluster transfer strategy in a hybridisation chain reaction-silver nanocluster hybrid sensor for nucleic acid detection.. Analytical methods : advancing methods and applications, 18(7), 1392-1396. https://doi.org/10.1039/d5ay01362c
MLA New SY, et al.. "Employing a cluster transfer strategy in a hybridisation chain reaction-silver nanocluster hybrid sensor for nucleic acid detection.." Analytical methods : advancing methods and applications, vol. 18, no. 7, 2026, pp. 1392-1396.
PMID 41627257
DOI 10.1039/d5ay01362c

Abstract

The hybridisation chain reaction (HCR) is a robust isothermal amplification technique widely used for nucleic acid detection, often paired with silver nanoclusters (AgNCs) for fluorescence-based readouts. However, conventional HCR-AgNC assays are prone to circuit leakage and unpredictable AgNC formation, which can compromise assay reliability. In this study, we present a modular HCR-AgNC hybrid sensor employing a cluster transfer strategy, in which pre-formed AgNCs are introduced separately into the HCR system. This design minimises interference between AgNCs and HCR components, enhancing signal specificity and predictability. Using a DNA analogue of miRNA-141 (DNA-141), a potential prostate cancer biomarker, we demonstrate selective red fluorescence activation upon target recognition. The sensor design was guided by NUPACK simulations, reducing trial-and-error and lowering assay costs. Gel electrophoresis and fluorescence spectroscopy confirmed the system's specificity and sensitivity, achieving a limit of detection of 46 nM. This work establishes a foundational framework for modular and adaptable nucleic acid biosensing, with potential for future sensitivity enhancements and multiplexed detection.

MeSH Terms

Silver; Metal Nanoparticles; Humans; MicroRNAs; Biosensing Techniques; Nucleic Acid Hybridization; Nucleic Acid Amplification Techniques; Limit of Detection; Male; Spectrometry, Fluorescence; Nucleic Acids