Evidence map›Paper›PMID 42819021›Full record

ArticleResearch square2026

Structural insights into ligand-induced CARD assembly in inflammatory caspases.

Zhongyi Jiang, Jun Bae Park, Youn Jung Choi, Stephanie Kim, Masaru Miyagi, Stephanie Leon Quinonez, Jae U Jung

Abstract readPreprint
In one paragraph

Article in Research square, 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.

Zhongyi JiangDepartment of Microbial Sciences in Health, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-4436-5605
Jun Bae ParkDepartment of Microbial Sciences in Health, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.
Youn Jung ChoiGlobal Center for Pathogen and Human Health Research, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0001-6879-0115
Stephanie KimGlobal Center for Pathogen and Human Health Research, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.
Masaru MiyagiDepartment of Pharmacology, Case Western Reserve University, Cleveland, Ohio, USA.ORCID 0000-0003-4325-1216
Stephanie Leon QuinonezDepartment of Microbial Sciences in Health, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-2437-0896
Jae U JungDepartment of Microbial Sciences in Health, Cleveland Clinic Research, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0003-4559-8774

Funding

Acquisition of a dedicated and integrated HD-MS instrumentS10OD036418 · OD · CASE WESTERN RESERVE UNIVERSITY · PI MIYAGI, MASARU · 2025 to 2025
$750k
Cleveland Clinic integrative behavior-single cell proteomics workflowS10OD025207 · OD · CLEVELAND CLINIC LERNER COM-CWRU · PI DESILVA, TARA MARIA · 2019 to 2019
$745k
NIH HHS S10 OD025207NIH HHS S10 OD036418
6 · The paper itself

Abstract

Non-canonical inflammatory caspases detect cytosolic lipopolysaccharide (LPS) through its caspase activation and recruitment domain (CARD), yet how ligand binding drives higher-order CARD assembly remains poorly understood. Here, we identify CBM7, a minimal SERPINB1-derived peptide, that induces caspase-4 CARD oligomerization. CBM7 promotes formation of a previously unrecognized flexible filament-like CARD architecture distinct from canonical CARD assemblies. Peptide- and LPS-induced CARD assembly require overlapping structural determinants, suggesting that structurally distinct ligands share common features in promoting higher-order CARD assembly. CBM7 also promotes oligomerization across inflammatory caspase CARDs and induces caspase activation, pyroptosis, and inflammatory responses in cells and mice. Together, these findings provide structural insight into ligand-induced inflammatory caspase CARD assembly and establish CBM7 as a chemically defined probe for dissecting the structural basis of inflammatory caspase activation.

Identifiers

PMID42819021
PMCPMC13622861

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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.