Evidence map›Paper›PMID 38280942›Full record

ArticleCommunications biology2024

M13 phage grafted with peptide motifs as a tool to detect amyloid-β oligomers in brain tissue.

Ivone M Martins, Alexandre Lima, Wim de Graaff, Joana S Cristóvão, Niek Brosens, Eleonora Aronica, Leon D Kluskens, Cláudio M Gomes, Joana Azeredo, Helmut W Kessels

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Amyloid-β-Driven Synaptic Deficits Are Mediated by Synaptic Removal of GluA3-Containing AMPA Receptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. 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

10 authors at 4 institutions in 2 countries.

Ivone M Martins *CEB- Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal. ivone.martins@ceb.uminho.pt.ORCID 0000-0002-3412-9377
Alexandre Lima *CEB- Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal.
Wim de GraaffSwammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Joana S CristóvãoBiosystems & Integrative Sciences Institute, Faculdade de Ciências, Universidade de Lisboa, Lisboa, Portugal.
Niek BrosensSwammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Eleonora AronicaAmsterdam UMC location University of Amsterdam, Department of (Neuro)Pathology, Amsterdam Neuroscience, Amsterdam, the Netherlands.ORCID 0000-0002-3542-3770
Leon D KluskensCEB- Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal.
Cláudio M GomesBiosystems & Integrative Sciences Institute, Faculdade de Ciências, Universidade de Lisboa, Lisboa, Portugal.ORCID 0000-0003-4662-6933
Joana AzeredoCEB- Centre of Biological Engineering, University of Minho, 4710-057, Braga, Portugal.ORCID 0000-0002-5180-7133
Helmut W KesselsNetherlands Institute for Neuroscience, Amsterdam, the Netherlands. h.w.h.g.kessels@uva.nl.ORCID 0000-0002-1122-745X
Netherlands Institute for Neuroscience · NLUniversity of Lisbon · PTUniversity of Minho · PTAmsterdam Neuroscience · NL

Funding

Alzheimer Nederland (Alzheimer Netherlands) WE.03-2020-06
6 · The paper itself

Abstract

Oligomeric clusters of amyloid-β (Aβ) are one of the major biomarkers for Alzheimer's disease (AD). However, proficient methods to detect Aβ-oligomers in brain tissue are lacking. Here we show that synthetic M13 bacteriophages displaying Aβ-derived peptides on their surface preferentially interact with Aβ-oligomers. When exposed to brain tissue isolated from APP/PS1-transgenic mice, these bacteriophages detect small-sized Aβ-aggregates in hippocampus at an early age, prior to the occurrence of Aβ-plaques. Similarly, the bacteriophages reveal the presence of such small Aβ-aggregates in post-mortem hippocampus tissue of AD-patients. These results advocate bacteriophages displaying Aβ-peptides as a convenient and low-cost tool to identify Aβ-oligomers in post-mortem brain tissue of AD-model mice and AD-patients.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsBacteriophage M13BrainHumansMiceMice, TransgenicAmyloid beta-PeptidesAmyloid beta-Protein Precursor

Identifiers

PMID38280942
PMCPMC10821927
OpenAlexW4391278232

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.