Evidence map›Paper›PMID 30894604›Full record

ArticleScientific reports2019

Inhibition of NLRP3 inflammasome activation by cell-permeable stapled peptides.

Arumay Pal, Kurt Neo, Lakshminarayanan Rajamani, Fernando Jose Ferrer, David P Lane, Chandra S Verma, Alessandra Mortellaro

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
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

7 citing papers in PubMed, 21 citations in OpenAlex.

  1. Insight into Protein Engineering: FromCurrent pharmaceutical design · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Identification of NLRP3International journal of molecular sciences · 2022
    Article
  6. Review
  7. Article
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 at 2 institutions in 2 countries.

Arumay PalBioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), 30 Biopolis Street, #07-01 Matrix, Singapore, 138671, Singapore.
Kurt NeoSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), 8a Biomedical Grove, Singapore, 138648, Singapore.
Lakshminarayanan RajamaniSingapore Eye Research Institute (SERI), The Academia, 20 College Road, Discovery Tower Level 6, Singapore, 169856, Singapore.ORCID 0000-0001-8214-5315
Fernando Jose Ferrerp53Lab, Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, #06-04/05 Neuros/Immunos, Singapore, 138648, Singapore.
David P Lanep53Lab, Agency for Science, Technology and Research (A*STAR), 8A Biomedical Grove, #06-04/05 Neuros/Immunos, Singapore, 138648, Singapore.ORCID 0000-0003-0551-3545
Chandra S VermaBioinformatics Institute (BII), Agency for Science, Technology and Research (A*STAR), 30 Biopolis Street, #07-01 Matrix, Singapore, 138671, Singapore. chandra@bii.a-star.edu.sg.
Alessandra MortellaroSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), 8a Biomedical Grove, Singapore, 138648, Singapore. mortellaro.alessandra@hsr.it.ORCID 0000-0003-1744-2430
Agency for Science, Technology and Research · SGSingapore Eye Research Institute · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-1β (IL-1β) is a major cytokine that initiates and enhances inflammatory responses. Excessive IL-1β production is a characteristic of most chronic inflammatory diseases, including atherosclerosis, type 2 diabetes, and obesity, which affect a large proportion of the global population. The production of bioactive IL-1β is mediated by a caspase-1-activating complex known as an 'inflammasome'. The NLRP3 inflammasome has been associated with several human inflammatory and autoimmune diseases and represents a potential therapeutic target for disrupting IL-1β production. We used molecular modeling guided by molecular dynamics simulations to design α-helical stapled peptides targeting the pyrin domain of the adaptor protein ASC to interrupt the development of its filament, which is crucial for NLRP3 inflammasome formation. The peptides were effectively internalized by human monocytic cells and efficiently suppressed the release of the inflammasome-regulated cytokines IL-1β and IL-18, following exogenous activation of the NLRP3 inflammasome. The peptides reduced ASC speck formation and caspase-1 processing thereby suppressing pro-IL-1β processing and release of active IL-1β. This is the first demonstration of the successful use of stapled peptides designed to target the adaptor protein ASC, and can be extended to other inflammatory pathways to disrupt excessive IL-1β production.

Indexed as

Binding SitesCARD Signaling Adaptor ProteinsCell-Penetrating PeptidesGene Expression RegulationHumansHydrophobic and Hydrophilic InteractionsInflammasomesInterleukin-18Interleukin-1betaLipopolysaccharidesModels, MolecularNF-kappa BNigericinNLR Family, Pyrin Domain-Containing 3 ProteinProof of Concept StudyProtein BindingCARD Signaling Adaptor ProteinsCell-Penetrating PeptidesIL1B protein, humanInflammasomesInterleukin-18Interleukin-1betaLipopolysaccharidesNF-kappa BNigericinNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanPYCARD protein, humanReactive Oxygen Species

Identifiers

PMID30894604
PMCPMC6426897
OpenAlexW2924700186

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.