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Record W7117165336 · doi:10.1002/alz70855_100417

An International Antibody Characterization Platform Enabling Alzheimer's Disease Research

2025· article· en· W7117165336 on OpenAlexaff
Riham Ayoubi, Aled M Edwards, Peter S. McPherson, Carl Laflamme

Bibliographic record

VenueAlzheimer s & Dementia · 2025
Typearticle
Languageen
FieldMedicine
TopicAlzheimer's disease research and treatments
Canadian institutionsUniversity of TorontoMontreal Neurological Institute and Hospital
Fundersnot available
KeywordsDiseaseCharacterization (materials science)AntibodyMEDLINEAntibody therapyHuman disease

Abstract

fetched live from OpenAlex

BACKGROUND: Understanding Alzheimer's disease (AD) etiology requires a comprehensive molecular and biological investigation of the estimated 184 genes/proteins linked to AD risk. However, most AD research focuses on 3 genes, APP, APOE, and TAU, which receive 49% of all AD-related PubMed hits. This highlights the need for a broader exploration of AD risk factors. A major challenge in this regard is the limited availability of selective and renewable antibodies for studying all AD-associated proteins. The Target Enablement to Accelerate Therapy Development for Alzheimer's Disease (TREAT-AD) program focuses on developing or identifying high-quality research tools for less-studied AD-associated proteins, enabling hypothesis testing (Axtman et al., Alzheimers Dement, 2023). METHOD: Antibody Characterization through Open Science (YCharOS) is an international, public-good initiative that unites academic researchers, funding agencies, leading antibody manufacturers and knockout cell line providers to evaluate antibody performance (Ayoubi et al., Nature Protocols, 2024). Using knockout cell lines as isogenic controls, antibodies from multiple manufacturers are tested side-by-side in western blot, immunoprecipitation and immunofluorescence. Results are disseminated openly and rapidly via the AD Knowledge Portal (https://adknowledgeportal.synapse.org/). RESULT: To date, 441 antibodies targeting 41 community-prioritized AD targets have been characterized. Most cited antibodies for these proteins are polyclonal and often lack specificity, particularly in immunofluorescence experiments. However, our findings reveal that selective and renewable antibodies, many of which are newly generated and rarely used in published studies, were available for 90% of TREAT-AD targets. When all existing antibodies for a protein underperform, TREAT-AD generates recombinant proteins as antigens for antibody development, collaborating with YCharOS partners for antibody production. This approach has been applied to AD-related proteins, including SMOC1, yielding recombinant antibodies with superior selectivity over existing ones. Using knockout-validated antibodies, we demonstrated that the proteins CD44, Moesin, sFRP-1 and Midkine, identified through systems biology by the TREAT-AD initiative as having altered gene expression in AD, are upregulated under disease conditions in AD mouse models (Doolen et al. F1000Research, 2024). CONCLUSION: YCharOS has established characterization standards that align with funding and journal requirements, and is committed to identify reliable and accessible tools for AD research.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.012
metaresearch head score (Gemma)0.006
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.018
Threshold uncertainty score0.063

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0120.006
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0050.002
Science and technology studies0.0010.001
Scholarly communication0.0030.003
Open science0.0020.004
Research integrity0.0020.003
Insufficient payload (model declined to judge)0.0180.021

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.065
GPT teacher head0.407
Teacher spread0.342 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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