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A Method for Selecting Structure-switching Aptamers Applied to a Colorimetric Gold Nanoparticle Assay
Published on: February 28, 2015
Stability matters: evaluating the long-term performance of AuNP-DNA conjugates in lateral flow assays through varied
Celia Fuentes-Chust1, Claudio Parolo2, Andrew Piper1
1Nanobioelectronics and Biosensors Group, Institut Català de Nanociència i Nanotecnologia (ICN2). UAB Campus, Bellaterra, Barcelona 08193, Spain. arben.merkoci@icn2.cat.
Abstract:
This study evaluates five distinct conjugation techniques for attaching DNA to gold nanoparticles (AuNPs), focusing on their applicability in lateral flow assays (LFA). The selected methods include three salt-aging techniques, one polyT-adsorption method, and a rapid butanol dehydration (INDEBT) approach. These methods were chosen based on factors such as popularity, protocol duration, and ionic strength. Additionally, the study investigates the storage stability of DNA-AuNP conjugates in four different buffers: 100 mM Tris-MgCl2, 10 mM PBS-MgCl2, PBS, and deionized water. These buffers were selected to evaluate the effects of ionic strength and their compatibility with LFA materials on conjugate stability and performance. Results indicate that salt-aging methods, particularly with water or PBS, maintained LFA functionality up to 21 days. Adsorbed DNA and all samples stored in PBS-MgCl2 were not functional from the start and aggregated over time. INDEBT and Tris-MgCl2 conjugates demonstrated initial functionality but degraded due to butanol residues and aggregation. A complementary analysis using electrophoretic mobility shift assays (EMSAs), UV-Vis spectroscopy, and dynamic light scattering (DLS) provided essential insights into conjugate behavior. These results emphasize the importance of buffer selection and conjugation techniques for optimizing DNA-AuNP conjugates in LFAs, ensuring their reliability and effectiveness in diagnostic applications.

