Upconversion-Linked Immunosorbent Assay for the Biomimetic Detection of the Mycotoxin Cyclopiazonic Acid

The neurotoxin α-cyclopiazonic acid (CPA) is an emerging mycotoxin produced as a secondary metabolite by several fungi species (<i>i.e</i>., <i>Penicillium</i> spp. and <i>Aspergillus</i> spp.). CPA commonly contaminates maize, crops, cheese, and wine. In this work, CPA detection in foodstuff was accomplished by the innovative integration of two strategies: upconversion nanoparticles (UCNPs) and epitope-mimicking peptides, to develop a competitive upconversion-linked immunosorbent assay (ULISA). We have applied UCNPs (type NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>) as background-free optical labels due to their anti-Stokes shift with excitation in the near-infrared region and emission in the ultraviolet-visible region. Moreover, a CPA epitope-mimicking cyclic peptide (A2) was used as a substitute for the toxin-conjugates traditionally applied to competitive assays. UCNPs were decorated with an anti-CPA fragment antigen-binding antibody (UCNP-Fab), and CPA detection was achieved through competition with a biotinylated CPA epitope-mimicking cyclic peptide (A2-biotin, ACNWWDLTLC-GGGSK (Biotin)-NH<sub>2</sub>), anchored to a streptavidin-coated microtiter plate, for antibody binding. The ULISA platform offers ultrasensitive detection of CPA (limit of detection of 1.3 pg mL<sup>-1</sup> and IC<sub>50</sub> value of 15 pg mL<sup>-1</sup>), and no cross-reactivity was observed with other coproduced mycotoxins. These results substantially outperformed the analytical features of conventional heterogeneous immunoassays based on enzymatic detection. Additionally, the use of advanced computational tools, such as MOE and Alphafold AI, proved advantageous in elucidating the molecular interactions between the antibody and the epitope, providing insights that enhance the rational design of immunoassays. The proposed ULISA was applied to detect CPA in spiked maize samples, and the results were validated by high-performance liquid chromatography coupled to a tandem mass spectrometry detector (HPLC-MS/MS).

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Publication Details

Journal
Analytical Chemistry
Published
2024-12-07
DOI
https://doi.org/10.1021/acs.analchem.4c05168
Citations
3
Primary Topic
Mycotoxins in Agriculture and Food
Type
article
Field-Weighted Citation Impact
1.80

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article

Upconversion-Linked Immunosorbent Assay for the Biomimetic Detection of the Mycotoxin Cyclopiazonic Acid

Riikka Peltomaa, Elena Benito‐Peña, Yoel Rodrı́guez, Satu Lahtinen et al.
3 citations
Analytical Chemistry
Mycotoxins in Agriculture and Food
1.80
article

Upconversion-Linked Immunosorbent Assay for the Biomimetic Detection of the Mycotoxin Cyclopiazonic Acid

Riikka Peltomaa, Elena Benito‐Peña, Yoel Rodrı́guez, Satu Lahtinen, Álvaro Luque‐Uría, Tero Soukka, Fernando Pradanas-González, Chris M. Maragos, María C. Moreno‐Bondi, Fernando Navarro-Villoslada
article en
3 citations

Abstract

The neurotoxin α-cyclopiazonic acid (CPA) is an emerging mycotoxin produced as a secondary metabolite by several fungi species (<i>i.e</i>., <i>Penicillium</i> spp. and <i>Aspergillus</i> spp.). CPA commonly contaminates maize, crops, cheese, and wine. In this work, CPA detection in foodstuff was accomplished by the innovative integration of two strategies: upconversion nanoparticles (UCNPs) and epitope-mimicking peptides, to develop a competitive upconversion-linked immunosorbent assay (ULISA). We have applied UCNPs (type NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>) as background-free optical labels due to their anti-Stokes shift with excitation in the near-infrared region and emission in the ultraviolet-visible region. Moreover, a CPA epitope-mimicking cyclic peptide (A2) was used as a substitute for the toxin-conjugates traditionally applied to competitive assays. UCNPs were decorated with an anti-CPA fragment antigen-binding antibody (UCNP-Fab), and CPA detection was achieved through competition with a biotinylated CPA epitope-mimicking cyclic peptide (A2-biotin, ACNWWDLTLC-GGGSK (Biotin)-NH<sub>2</sub>), anchored to a streptavidin-coated microtiter plate, for antibody binding. The ULISA platform offers ultrasensitive detection of CPA (limit of detection of 1.3 pg mL<sup>-1</sup> and IC<sub>50</sub> value of 15 pg mL<sup>-1</sup>), and no cross-reactivity was observed with other coproduced mycotoxins. These results substantially outperformed the analytical features of conventional heterogeneous immunoassays based on enzymatic detection. Additionally, the use of advanced computational tools, such as MOE and Alphafold AI, proved advantageous in elucidating the molecular interactions between the antibody and the epitope, providing insights that enhance the rational design of immunoassays. The proposed ULISA was applied to detect CPA in spiked maize samples, and the results were validated by high-performance liquid chromatography coupled to a tandem mass spectrometry detector (HPLC-MS/MS).

Analytical ChemistryVol. 96(50)
Universidad Complutense de Madrid (ES), Agricultural Research Service (US), University of Turku (FI), City University of New York (US), National Center for Agricultural Utilization Research (US), Hostos Community College (US), Icahn School of Medicine at Mount Sinai (US)
Ministerio de Ciencia, Innovación y Universidades
Zero hunger
Openalex Percentile: Top 12%
Mycotoxins in Agriculture and Food
1.80
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