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Updated: Dec 22, 2025

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as A Novel Detection and Quantification Method
Published on: October 7, 2025
DNA-Driven Two-Layer Core-Satellite Gold Nanostructures for Ultrasensitive MicroRNA Detection in Living Cells
Dan Meng1, Wei Ma1, Xiaoling Wu1
1International Joint Research Laboratory for Biointerface and Biodetection State Key Lab of Food Science and Technology School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, 214122, P. R. China.
Abstract:
It is a significant challenge to achieve controllable self-assembly of superstructures for biological applications in living cells. Here, a two-layer core-satellite assembly is driven by a Y-DNA, which is designed with three nucleotide chains that hybridized through complementary sequences. The two-layer core-satellite nanostructure (C30 S5 S10 NS) is constructed using 30 nm gold nanoparticles (Au NPs) as the core, 5 nm Au NPs as the first satellite layer, and 10 nm Au NPs as the second satellite layer, resulting in a very strong circular dichroism (CD) and surface-enhanced Raman scattering. After optimization, the yield is up to 85%, and produces a g-factor of 0.16 × 10-2 . The hybridization of the target microRNA (miRNA) with the molecular probe causes a significant drop in the CD and Raman signals, and this phenomenon is used to detect the miRNA in living cells. The CD signal has a good linear range of 0.011-20.94 amol ngRNA-1 and a limit of detection (LOD) of 0.0051 amol ngRNA-1 , while Raman signal with the range of 0.052-34.98 amol ngRNA-1 and an LOD of 2.81 × 10-2 amol ngRNA-1 . This innovative dual-signal method can be used to quantify biomolecules in living cells, opening the way for ultrasensitive, highly accurate, and reliable diagnoses of clinical diseases.
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