Evidence map›Paper›PMID 42252772›Full record

ArticleChembiochem : a European journal of chemical biology2026

Mapping the Substrate Specificity Landscape of PAD2 and PAD4 Enzymes.

Adina Borbély, Arnold Steckel, Dávid Papp, Domonkos Pál, Katalin Uray, Viktória Goldschmidt Gőz, Gitta Schlosser

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 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.

Adina BorbélyMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Arnold SteckelMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Dávid PappMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Domonkos PálMTA-TTK Lendület (Momentum) Glycan Biomarker Research Group, HUN-REN Research Centre for Natural Sciences, Budapest, Hungary.
Katalin UrayMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Viktória Goldschmidt GőzMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.
Gitta SchlosserMTA-ELTE Lendület (Momentum) Ion Mobility Mass Spectrometry Research Group, Department of Analytical Chemistry, Institute of Chemistry, ELTE Eötvös Loránd University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-7637-7133

Funding

Innovációs és Technológiai Minisztérium TKP2020-NKA-06Magyar Tudományos Akadémia Momentum ProgrammeNemzeti Kutatási, Fejlesztési és Innovaciós Alap 2018-1.2.1-NKP-2018-00005
6 · The paper itself

Abstract

Pathological citrullination of proteins is implicated in several diseases, including rheumatoid arthritis, neurodegenerative disorders, and cancer. This irreversible post-translational modification is driven by the peptidyl arginine deiminase (PAD) enzyme family. Although the substrate specificity of the key PAD2 and PAD4 isotypes has been studied, the detailed role of individual amino acids from a multidimensional perspective remains unexplored. Here, we designed a combinatorial library of 256 synthetic peptides to comprehensively map PAD2 and PAD4 substrate preferences. Sixteen natural amino acids were examined in positions flanking the target arginine residue using combinatorial peptide mixtures produced by a split-and-mix synthetic strategy. Relative citrullination efficiencies following PAD treatment were analyzed using mass spectrometry, enhanced by cyclic ion mobility separation. PAD4 displayed higher substrate selectivity than PAD2. PAD2 efficiently citrullinated 233 of the 256 peptides, reaching ≥92% efficiency, with Glu and Pro in the C-terminal position of the target arginine being unfavorable. In contrast, PAD4 showed lower overall conversion, with Pro strongly inhibiting citrullination at the C-terminal position and multiple residues negatively affecting the N-terminal position. Notably, Asn at either flanking position enhanced citrullination for both PAD enzymes. These findings highlighted the need to differentiate arginine citrullination from asparagine deamidation for accurate identification.

Indexed as

HydrolasesPeptidesAmino Acid SequenceArginineCitrullinationHumansPeptide LibraryProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 2Protein-Arginine Deiminase Type 4Substrate SpecificityArginineHydrolasesPADI2 protein, humanPADI4 protein, humanPeptide LibraryPeptidesProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 2Protein-Arginine Deiminase Type 4citrullinationcombinatorial librarymass spectrometryPAD2PAD4

Identifiers

PMID42252772
PMCPMC13243971

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.