Evidence map›Paper›PMID 40240579›Full record

ArticleMikrochimica acta2025

Biotechnology-enhanced immunoassay for accurate determination of HT-2 toxin in edible insect samples.

Raúl Sancho-García, Fernando Navarro-Villoslada, Fernando Pradanas-González, Henri O Arola, Bettina Glahn-Martínez, Tarja K Nevanen, Elena Benito-Peña

Erratum issuedAbstract read
In one paragraph

Article in Mikrochimica acta, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Raúl Sancho-García *Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, Madrid, 28040, Spain.
Fernando Navarro-Villoslada *Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, Madrid, 28040, Spain.ORCID 0000-0002-6149-7511
Fernando Pradanas-GonzálezDepartment of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, Madrid, 28040, Spain.ORCID 0000-0002-0727-7737
Henri O ArolaVTT Technical Research Centre of Finland Ltd, Tekniikantie 21, Espoo, 02044, Finland.ORCID 0000-0002-4931-2529
Bettina Glahn-MartínezDepartment of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, Madrid, 28040, Spain. ab.glahn@ucm.es.ORCID 0000-0003-0128-3113
Tarja K NevanenVTT Technical Research Centre of Finland Ltd, Tekniikantie 21, Espoo, 02044, Finland.ORCID 0000-0001-8964-1012
Elena Benito-PeñaDepartment of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense de Madrid, Plaza de las Ciencias, Ciudad Universitaria, Madrid, 28040, Spain. elenabp@ucm.es.ORCID 0000-0001-5685-5559

Funding

European Union's Horizon Europe EICPathfinder Open programme 101046787European Union's MSCA Staff exchange Horizon Europe programme 101086341Spanish Ministry of Science and Innovation PID2021-127457OB-C21
6 · The paper itself

Abstract

Consumption of edible insects is common in non-Western countries of Africa, Asia, Oceania, and Latin America. However, their consumption has significantly increased in Europe in recent years thanks to their remarkable nutritional properties. Edible insects provide a valuable source of high-quality proteins, fats, minerals, and vitamins. Nevertheless, the absence of global regulatory guidelines poses a risk associated with their consumption due to the potential presence of pathogens and contaminants, such as mycotoxins, which are toxic compounds produced by fungi and represent a major threat to food and feed safety. Our approach integrates advanced nanobiotechnology to develop fluorescent antibodies by conjugating a recombinant superfolder green fluorescent protein (sfGFP) with a single-chain antibody (scFv). This fusion allows for precise detection of the immune complex formed between the HT-2 toxin and a biotinylated anti-HT-2 antibody. Additionally, we employed advanced computational tools, including AlphaFold and MOE, to deepen our understanding of the binding interactions present in the immune complex, confirming the strong interaction between the Fab/HT-2 toxin immunocomplex and the scFv antibody fragment, in contrast to the weaker binding observed with the Fab/T-2 toxin and the scFv. The method demonstrates high sensitivity, with an EC

Indexed as

Edible InsectsFood ContaminationT-2 ToxinAnimalsGreen Fluorescent ProteinsImmunoassayLimit of DetectionSingle-Chain AntibodiesGreen Fluorescent ProteinsHT-2 toxinSingle-Chain AntibodiesT-2 ToxinCricket flourEdible insectsFood safetyHT-2 toxinImmune complexNon-competitive immunoassay

Identifiers

PMID40240579
PMCPMC12433359

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.