Evidence map›Paper›PMID 41431195›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

MARPLE: A Proximity-Triggered CRISPR-Cas13 Platform for Ultrasensitive Antibody Detection.

Elena Spezzani, Luca Capelli, Denise Di Lena, Alejandro Chamorro-Garcia, Rudy Ippodrino, Alessandro Porchetta, Alessandro Bertucci

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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.

Elena SpezzaniDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID https://orcid.org/0009-0008-0533-1374
Luca CapelliDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID https://orcid.org/0000-0001-5002-1844
Denise Di LenaDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID https://orcid.org/0009-0004-2361-4782
Alejandro Chamorro-GarciaDepartment of Sciences and Chemical Technologies, University of Rome Tor Vergata, Rome, Italy.
Rudy IppodrinoUlisse BioMed Laboratories, Trieste, Italy.
Alessandro PorchettaDepartment of Sciences and Chemical Technologies, University of Rome Tor Vergata, Rome, Italy.ORCID https://orcid.org/0000-0002-4061-5574
Alessandro BertucciDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy.ORCID https://orcid.org/0000-0003-4842-9909

Funding

'Departments of Excellence' program of the Italian Ministry for University and Research MUR 2023-2027Fondazione AIRC per la ricerca sul cancro ETS 31108National Recovery and Resilience Plan
6 · The paper itself

Abstract

Monitoring clinically relevant antibodies-as biomarkers of disease or therapeutic response-is essential for informed clinical decision-making. Traditional immunoassays like ELISA offer reliable quantification but often involve multistep workflows and limited point-of-care utility. New approaches coupling antibody recognition with signal amplification are therefore highly desirable. The CRISPR-Cas13 system, known for its potent collateral cleavage activity, has emerged as a powerful diagnostic tool for nucleic acid detection. However, its application to protein biomarkers such as antibodies remains underdeveloped. Here, we introduce MARPLE (Modular Antibody Recognition via Proximity-triggered Linker Exchange), a modular CRISPR-Cas13-based platform for ultrasensitive antibody detection. MARPLE harnesses antibody-induced proximity to trigger a strand displacement reaction that releases a sequestered RNA target, activating Cas13-mediated collateral cleavage of fluorescent RNA reporters. This cascade enables detection of antibodies at femtomolar concentrations. We demonstrate MARPLE's versatility across diverse targets-including anti-digoxigenin, anti-cholesterol, anti-HA, trastuzumab, and anti-MUC1-highlighting applications in infectious disease monitoring, cancer diagnostics, and therapeutic drug tracking. The assay is isothermal, one-pot, and retains robust performance in complex matrices such as human serum. These features establish MARPLE as a promising tool for immunodiagnostics, extending CRISPR-based sensing beyond nucleic acids to protein biomarker detection.

Indexed as

AntibodiesCRISPR-Cas SystemsHumansImmunoassayAntibodiesantibodyCRISPR‐Cas13DNA nanotechnologyimmunoassayproximity assay

Identifiers

PMID41431195
PMCPMC12955873

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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.