Evidence map›Paper›PMID 35056853›Full record

ArticleMolecules (Basel, Switzerland)2022

Utilizing the DNA Aptamer to Determine Lethal α-Amanitin in Mushroom Samples and Urine by Magnetic Bead-ELISA (MELISA).

Jiale Gao, Nuoya Liu, Xiaomeng Zhang, En Yang, Yuzhu Song, Jinyang Zhang, Qinqin Han

Open access · goldAbstract readValidation Study
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.8field-weighted citation impact, top 5% of its field
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

10 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Aptamer-functionalized polydiacetylene biosensor for the detection of three foodborne pathogens.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Jiale GaoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
Nuoya LiuFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
Xiaomeng ZhangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
En YangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
Yuzhu SongFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.ORCID 0000-0002-9836-0252
Jinyang ZhangFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.ORCID 0000-0001-7533-998X
Qinqin HanFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.
Kunming University of Science and Technology · CN

Funding

Basic research projects of Yunnan Province No. 202001AT070033, 140520210031National Natural Science Foundation of China No. 32160601
6 · The paper itself

Abstract

Amanita poisoning is one of the most deadly types of mushroom poisoning. α-Amanitin is the main lethal toxin in amanita, and the human-lethal dose is about 0.1 mg/kg. Most of the commonly used detection techniques for α-amanitin require expensive instruments. In this study, the α-amanitin aptamer was selected as the research object, and the stem-loop structure of the original aptamer was not damaged by truncating the redundant bases, in order to improve the affinity and specificity of the aptamer. The specificity and affinity of the truncated aptamers were determined using isothermal titration calorimetry (ITC) and gold nanoparticles (AuNPs), and the affinity and specificity of the aptamers decreased after truncation. Therefore, the original aptamer was selected to establish a simple and specific magnetic bead-based enzyme linked immunoassay (MELISA) method for α-amanitin. The detection limit was 0.369 μg/mL, while, in mushroom it was 0.372 μg/mL and in urine 0.337 μg/mL. Recovery studies were performed by spiking urine and mushroom samples with α-amanitin, and these confirmed the desirable accuracy and practical applicability of our method. The α-amanitin and aptamer recognition sites and binding pockets were investigated in an in vitro molecular docking environment, and the main binding bases of both were T3, G4, C5, T6, T7, C67, and A68. This study truncated the α-amanitin aptamer and proposes a method of detecting α-amanitin.

Indexed as

AgaricalesAlpha-AmanitinAptamers, NucleotideColorimetryEnzyme-Linked Immunosorbent AssayGoldHumansMagnetic PhenomenaMetal NanoparticlesMolecular Docking SimulationMushroom PoisoningSensitivity and SpecificityAlpha-AmanitinAptamers, NucleotideGoldaptamerMELISAmushroomtruncated aptamersurineα-amanitin

Identifiers

PMID35056853
PMCPMC8779134
OpenAlexW4205442679

What OpenQuestion holds

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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.