Evidence map›Paper›PMID 41182621›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Identifying Trypanosoma cruzi Proteins Targeted by Chagas Disease Patient Antibodies Using Yeast Surface Display.

Mira Loock, Igor Cestari

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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

2 authors.

Mira LoockInstitute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, QC, Canada.
Igor CestariInstitute of Parasitology, McGill University, Sainte-Anne-de-Bellevue, QC, Canada. igor.cestari@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding and identifying protein-ligand interactions is essential for elucidating fundamental biological processes and developing translational applications such as vaccine and drug targets. Yeast surface display (YSD) systems expressing genome-wide or combinatorial libraries in Saccharomyces cerevisiae are powerful tools to identify protein-ligand interactions in an unbiased fashion. In the following protocol, we couple the YSD system expressing a genome-wide library of the protozoan pathogen Trypanosoma cruzi with magnetic-activated cell sorting to identify antigen-antibody interactions. We describe the enrichment of pathogen antigens targeted by antibodies of infected patients using the YSD library. We also detailed a DNA sequencing methodology and a data analysis computational pipeline. The approach can be easily adapted to identify protein-protein or protein-drug interactions.

Indexed as

Antibodies, ProtozoanCell Surface Display TechniquesChagas DiseaseProtozoan ProteinsSaccharomyces cerevisiaeTrypanosoma cruziAntigens, ProtozoanGene LibraryHumansAntibodies, ProtozoanAntigens, ProtozoanProtozoan ProteinsAntibody screenAntigenLigand interactionMagnetic-activated cell sortingProteinT. cruzi antigen profilingVaccine target identificationYeast surface display

Identifiers

PMID41182621

What OpenQuestion holds

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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.