4.7 Article

Entrapping gold nanoparticles in membranes for simple-to-use enhanced fluorescence detection of proteins

Journal

ANALYTICA CHIMICA ACTA
Volume 1195, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2022.339443

Keywords

Metal enhanced fluorescence; Gold nanoparticles (AuNPs); Membrane; Immunoassay; Protein

Funding

  1. University of Guelph

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Quantifying proteins is important for understanding human health and disease, and sensitive protein quantification techniques are required for disease diagnosis. This study presents a novel signal enhancement method for fluorescence-based protein detection using gold nanoparticles on a nitrocellulose membrane. It achieved metal enhanced fluorescence and improved the sensitivity of protein quantification.
Quantifying proteins under different physiological and pathological conditions can give important in-sights into human health and disease, since proteins are the functional components of cells. In order to be able to use protein expression levels to diagnose diseases, sensitive protein quantification techniques are required, because some proteins can be present in low concentrations in biofluids at early stages of a disease. Here, a novel and simple-to-implement signal enhancement method for fluorescence-based protein detection is presented, in which an immunoassay was conducted on a nitrocellulose mem-brane, and a solution of gold nanoparticles was then pipetted onto the membrane before signal acqui-sition with a fluorescence microscope. The gold nanoparticles were entrapped and adsorbed into the 3D membrane matrix upon drying due to the hydrophobic interactions with the membrane. Through optimizing the concentration and size of the nanoparticles and comparison of different membranes, we were able to achieve metal enhanced fluorescence (MEF). This new gold nanoparticle-based MEF method, together with the 3D membrane platform that improves antibody and gold nanoparticle binding capacity, provided higher signal intensity and assay sensitivity for fluorescence-based protein quantifi-cation. Fluorescently-labeled IgG protein was spiked in human plasma with different concentrations, and the lower limit of detection was determined to be 29 ng/mL, three orders of magnitude lower than that of conventional 2D assays and one order of magnitude lower than that of 3D membrane assays without applying gold nanoparticles. This method offers a simple way of improving the sensitivity of fluorescence-based immunoassays that can be easily adopted in a biological lab with basic lab set up. Furthermore, it can be potentially extended to the fluorescence detection of other analytes beyond proteins. (c) 2022 Elsevier B.V. All rights reserved.

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