Evidence map›Paper›PMID 39753373›Full record

ArticleAnalytical chemistry2025

Decellularization and Enzymatic Digestion Methods to Enhance ECM Protein Detection via MALDI-MS Imaging.

Akaansha Rampal, Ina F de la Fuente, Ngoc K Vu, Jeerapat Doungchawee, Ujjwal Ranjan, Shelly R Peyton, Richard W Vachet

Abstract read
In one paragraph

Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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.

Akaansha RampalMolecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Ina F de la FuenteDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Ngoc K VuDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Jeerapat DoungchaweeDepartment of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Ujjwal RanjanRamoGnee Technologies, Gurugram, Haryana 132092, India.
Shelly R PeytonMolecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, Massachusetts 01003, United States.
Richard W VachetMolecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, Massachusetts 01003, United States.ORCID 0000-0003-4514-0210

Funding

Novel metabolomic contrast probes for human lung cancer characterizationR01CA273010 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FARRAR, CHRISTIAN T · 2022 to 2025
$3.3M
NCI NIH HHS R01 CA273010
6 · The paper itself

Abstract

Matrix-assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) has been used to generate spatial maps of lipids, metabolites, peptides, proteins, and glycans in tissues; however, its use for mapping extracellular matrix (ECM) protein distributions is underexplored. ECM proteins play a major role in various pathological conditions, and changes in their spatial distributions affect the function and morphology of cells within tissues. ECM protein detection is challenging because they are large, insoluble, and undergo various post-translational modifications, such as glycosylation. We describe here decellularization of tissue sections coupled with serial enzymatic digestions with PNGaseF and trypsin to improve ECM protein detection in MALDI-MSI without disrupting ECM architecture. Decellularization leads to a 3-fold increase in the number of proteins that are measured by MALDI-MSI. We also introduce a binary colocalization method to improve protein identification, which increases the number of proteins that are confidently detected. Together, these methods enhance the spatial mapping of ECM proteins by MALDI-MSI.

Indexed as

Extracellular Matrix ProteinsPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTrypsinAnimalsExtracellular MatrixExtracellular Matrix ProteinsPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseTrypsin

Identifiers

PMID39753373
PMCPMC12088692

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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.