{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/psoriasis_proteomics.xlsx"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F5.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F11.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F9.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F15.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F14.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F12.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F6.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F8.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F10.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F7.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD077433/Skin_F13.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["cyhsiang@mail.cmu.edu.tw"],"submitter":["Chiao-che Chen"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Syzygium aromaticum; eugenol; psoriasis; interleukin-17a; interleukin-36; proteomics","interleukin-36","proteomics","Syzygium aromaticum","psoriasis","interleukin-17a","eugenol"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD077433"],"tissue":["Skin"],"sample_protocol":["Total proteins were extracted from skin tissues using ice-cold radioimmunoprecipitation assay lysis buffer (50 mM Tris-HCl, 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, 0.1% sodium dodecyl sulfate, and 1 mM EDTA). Protein concentrations were determined using the Bradford assay (Protein Assay Dye Reagent, Bio-Rad, Hercules, CA, USA). To accommodate sample constraints and focus on exploratory proteomic screening, biological samples from five mice per group were pooled to create a single representative sample per experimental group (mock, IMQ, 200 mg/kg clove, and eugenol).  iTRAQ-based LC-MS/MS was performed as previously described (Liu et al., 2020). Briefly, protein extracts were digested with Trypsin Gold (Promega, Madison, WI, USA) and labeled using iTRAQ 8-plex reagents (Applied Biosystems, Foster City, CA, USA). Labeled peptides were analyzed using an UltiMate 3000 RSLCnano system coupled to an Orbitrap Exploris 480 mass spectrometer (Thermo Fisher Scientific, Waltham, MA, USA). Data processing and protein identification were performed using Proteome Discoverer (version 2.4, Thermo Scientific, Waltham, MA, USA). MS/MS spectra were searched against the UniProt Mus musculus database using the following parameters: trypsin as the protease with a maximum of two missed cleavages; precursor mass tolerances of 10 ppm; and fragment mass tolerance of 0.02 Da. Methylthio (C) and iTRAQ 8-plex (K and N-terminus) were defined as static modifications. Variable modifications included oxidation (M) and deamidation (N, Q), along with protein N-terminal modifications (acetylation, Met-loss, and Met-loss + acetylation). Representative MS/MS spectra and unique peptide sequences confirming the identification of IL-36α."],"repository":["pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["Protein quantification was based on the ratio of areas under the iTRAQ reporter ion peaks (117 for mock, 118 for IMQ, 119 for clove, and 121 for eugenol). Normalization was performed at the peptide level, where the intensities of all peptide-to-spectral matches were scaled to the median of the total peptide population to correct for potential loading bias. Final protein-level ratios were calculated as the median of the normalized peptide sequences assigned to each protein. Fold changes were determined by comparing iTRAQ reporter intensities among the experimental groups (IMQ vs. mock, and clove or eugenol vs. IMQ). The statistical significance of protein ratios was determined within Proteome Discoverer, which calculates p-values for protein ratios based on the distribution and variation of individual peptide ratios assigned to each protein. A one-sample Student's t-test was applied to the log-transformed ratios to test against a  null hypothesis of 1.0 (no change). Proteins were considered differentially expressed if they met a dual criterion of a Benjamini-Hochberg adjusted p-value < 0.05 and a linear fold change of ≥ 2 or ≤ -2. This threshold was chosen to minimize false positives and prioritize the most biologically substantial alterations for downstream functional analysis. Functional annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were conducted via the DAVID bioinformatics suite (https://davidbioinformatics.nih.gov/), with significance assessed using the Benjamini-Hochberg false discovery rate (FDR) correction (Sherman et al., 2022). Heatmaps were subsequently generated using Morpheus (https://software.broadinstitute.org/morpheus)."],"omics_type":["Proteomics"],"labhead":["Chien-Yun Hsiang"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Department of Microbiology and Immunology, China Medical University, Taichung 404328, Taiwan"],"species":["Mus Musculus (mouse)"],"publication":["Not available"],"submitter_mail":["march1990324@gmail.com"],"submitter_affiliation":["China Medical University"],"submitter_country":["Taiwan"],"additional_accession":[]},"is_claimable":false,"name":"Clove (Syzygium aromaticum) and its bioactive constituent eugenol alleviate psoriatic inflammation by modulating the IL-36/IL-17A axis: A proteomic and mechanistic study","description":"An imiquimod (IMQ)-induced psoriasis-like mouse model was employed to assess the therapeutic effects of orally administered clove extract and eugenol. iTRAQ-based LC–MS/MS proteomics were performed to identify molecular alterations, followed by bioinformatics 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