{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_ProteinGroups.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_ResultStatistics.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_PeptideGroups.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/checksum.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_Proteins.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_SpecializedTraces.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_PSMs.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_MSMSSpectrumInfo.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_QuanSpectra.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_InputFiles.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/420646_PrSMs.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/5.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/7.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/9.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/6.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/10.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079333/8.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["phdz2023@163.com"],"submitter":["Zhiqiang Zhang"],"technology_type":["Mass Spectrometry","Top-down proteomics"],"software":[""],"submitter_keywords":["nf-κb","Chronic sinusitis","Chronic sinusitis; epithelial-mesenchymal transition; dnajb9; ubiquitination; nf-κb","ubiquitination","epithelial-mesenchymal transition","dnajb9"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD079333"],"tissue":["Skin"],"sample_protocol":["Protein Extraction SDT buffer was added to the sample, and transferred to 2 ml tubes with an appropriate amount of quartz sand. The lysate was homogenized by an MP Fastprep-24 Automated Homogenizer (6.0 M/S, 30 s, twice). The homogenate was sonicated and then boiled for 10 min. After being centrifuged at 14,000 g for 15 min, the supernatant was filtered with 0.22 µm filters. The filtrate was quantified with the BCA Protein Assay Kit (Beyotime) and the sample was stored at -80 °C.  FASP Digestion and TMT Labeling For each sample, 150 µg of proteins were reduced with 100 mM DTT for 5 min at 100 °C. The detergent, DTT, and other low-molecular-weight components were removed using UA buffer (8 M Urea, 150 mM Tris-HCl pH 8.5) by repeated ultrafiltration (Sartorius, 30 kD). Then, 100 µl of iodoacetamide (100 mM IAA in UA buffer) was added to block reduced cysteine residues, and the samples were incubated for 30 min in darkness. The filters were washed with 100 µl UA buffer three times and then 100 µl 50 mM NH4HCO3 buffer twice. Finally, the protein suspensions were digested with 4 µg trypsin (Promega) in 40 µl 50 mM NH4HCO3 buffer overnight at 37 °C, and the resulting peptides were collected as a filtrate. The peptide segment was desalted by a C18 column, and the peptide content was estimated by UV light spectral density at 280 nm. Subsequently, 30 µg of the peptide mixture of each sample was labeled using a TMT reagent according to the manufacturer's instructions (Thermo Fisher Scientific).  High-pH Reversed-Phase Fractionation TMT-labeled peptides were fractionated by RP chromatography using the Agilent 1260 infinity II HPLC. The peptide mixture was diluted with buffer A (10 mM HCOONH4, 5% ACN, pH 10.0) and loaded onto an XBridge Peptide BEH C18 Column (130Å, 5 µm, 4.6 mm X 100 mm). The peptides were eluted at a flow rate of 1 ml/min with a gradient of buffer B (10 mM HCOONH4, 85% ACN, pH 10.0). The collected fractions were combined into 34 fractions, freeze-dried, reconstituted with 0.1% FA, and combined into 10 parts.  LC-MS/MS Analysis Each eluent was injected for nanoLC-MS/MS analysis twice. The peptide mixture was loaded onto the C18-reversed phase analytical column (Thermo Fisher Scientific, Acclaim PepMap RSLC 50 um X 15 cm, nano viper, P/N164943) in buffer A (0.1% Formic acid) and separated with a linear gradient of buffer B (80% acetonitrile and 0.1% Formic acid) at a flow rate of 300 nl/min. LC-MS/MS analysis was performed on a Q Exactive HF-X mass spectrometer (Thermo Fisher Scientific) coupled to Easy nLC for 120 min. The mass spectrometer was operated in positive ion mode, using a data-dependent top10 method dynamically choosing the most abundant precursor ions from the survey scan (350-1800 m/z) for HCD fragmentation. Survey scans were acquired at a resolution of 60,000 or 120,000 at m/z 200 with an AGC target of 3e6 and a maxIT of 50 ms. MS2 scans were acquired at a resolution of 17,500 or 45,000 for HCD spectra at m/z 200 with an AGC target of 1e5 and a maxIT of 50 ms, and an isolation width of 1.6 m/z. Only ions with a charge state between 2-6 and a minimum intensity of 8e3 were selected for fragmentation. Dynamic exclusion for selected ions was 30 s, and normalized collision energy was 31 eV."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["Database Search and Protein IdentificationMS/MS raw files were processed using the MASCOT engine (Matrix Science, London, UK; version 2.6) embedded into Proteome Discoverer 2.2 or 2.4, and searched against the designated database. The search parameters included trypsin as the enzyme used to generate peptides with a maximum of 2 missed cleavages permitted. A precursor mass tolerance of 10 ppm was specified, along with a 0.05 Da tolerance for MS2 fragments. Except for TMT labels, carbamidomethyl (C) was set as a fixed modification. Variable modifications included Oxidation (M) and Acetyl (Protein N-term). A peptide and protein false discovery rate of 1% was enforced using a reverse database search strategy.    Bioinformatics Analysis    Functional Annotation: The process of Gene Ontology (GO) annotation of target protein collections using Blast2GO (V1.4.4) was summarized into four steps: sequence alignment (Blast), GO terms extraction (Mapping), GO annotation, and supplementary annotation (ANNEX). Additionally, InterProScan (interproscan-5.30-69.0) was used to search the EBI database for conserved motifs. For KEGG pathway annotation, the KOALA (KEGG Orthology And Links Annotation, V3.0) software was used to align target protein sequences against the KEGG GENES database to automatically obtain pathway information. Functional domain annotation was performed using the Interpro database.      Enrichment Analysis: The enrichment analysis algorithms for GO annotations, KEGG pathway annotations, and functional domains were consistent. Based on Fisher's Exact Test, the distribution of each term in the target protein set was compared to the total protein set to evaluate the significance level of enrichment.      Subcellular Localization & Clustering: WoLF PSORT was used to predict the subcellular localization of proteins. Before cluster analysis, quantitative values were normalized, and the matplotlib package in Python was utilized to classify samples and protein expression (distance algorithm: Euclidean; connection method: Average linkage) to generate hierarchical clustering heat maps.      Network and GSEA Analysis: The direct or indirect interaction network between the target protein IDs was mapped using the String database and visualized with AnyChart software. Gene Set Enrichment Analysis (GSEA) was performed for all identified genes using GSEA software."],"omics_type":["Proteomics"],"labhead":["zhiqiang zhang"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["nanchang university"],"species":["Homo Sapiens (human)"],"publication":["Not available"],"submitter_mail":["phdz2023@163.com"],"submitter_affiliation":["Nanchang University"],"submitter_country":["China"],"additional_accession":[]},"is_claimable":false,"name":"DNAJB9 promotes epithelial-mesenchymal transition in the nasal epithelium of chronic rhinosinusitis by enhancing TRIM22-mediated IκBα degradation","description":"This study investigates the functional role of DNAJB9 in the pathogenesis of chronic rhinosinusitis with nasal polyps (CRSwNP). Using quantitative proteomics alongside human tissue analysis and murine models, we found that DNAJB9 is significantly upregulated in CRSwNP nasal epithelium and closely mirrors epithelial-mesenchymal transition (EMT) progression. Functional assays in human epithelial cells demonstrated that DNAJB9 actively drives the EMT phenotype. Mechanistically, DNAJB9 interacts with and stabilizes the E3 ubiquitin ligase TRIM22 by inhibiting its autoubiquitination. This stabilized TRIM22 targets IκBα for proteasomal degradation, leading to constitutive NF-κB pathway activation and subsequent EMT. Ultimately, DNAJB9 acts as an essential driver of tissue remodeling in CRSwNP. These findings highlight the broader clinical significance of the DNAJB9/TRIM22/NF-κB signaling axis, presenting it as a promising therapeutic target for inhibiting nasal polyp formation and associated remodeling.","dates":{"publication":"2026-06-17","submission":"2026-06-06"},"accession":"PXD079333","cross_references":{"TAXONOMY":["NEWT:330879","NEWT:377960","NEWT:1131","NEWT:2042546","NEWT:259447","NEWT:295546","NCBITaxon:2719036","NEWT:1334565","NEWT:625351","NEWT:258594","NCBITaxon:1280","NEWT:112503","NEWT:1129","NEWT:309807","NEWT:59753","NEWT:89184","NEWT:309800","NEWT:281395","NEWT:1211601","NEWT:876138","NEWT:44271","NEWT:193516","NEWT:1073882","NEWT:6819","NEWT:475174","NEWT:111205","NEWT:428386","NEWT:1117","NEWT:498257","NEWT:10036","NEWT:32264","NEWT:1590","NEWT:10034","NEWT:33114","NEWT:1596","NEWT:661410","NEWT:638632","NEWT:224326","NEWT:376619","NCBITaxon:79857","NEWT:1096976","NEWT:3765","NEWT:3767","NEWT:1589","NEWT:135622","NEWT:672127","NEWT:35786","NEWT:1580","NEWT:399784","NEWT:96731","NEWT:656064","NEWT:1582","NEWT:1584","NEWT:36630","NEWT:1585","NEWT:383379","NEWT:418106","NCBITaxon:12721","NEWT:10029","NEWT:913645","NEWT:2492962","NEWT:641809","NEWT:1392488","NEWT:38815","NEWT:317447","NEWT:4688","NEWT:111225","NEWT:7719","NEWT:5530","NEWT:868565","NEWT:135674","NEWT:79329","NEWT:30069","NEWT:12637","NEWT:59729","NEWT:2164133","NEWT:295105","NEWT:108061","NEWT:60711","NEWT:224308","NEWT:3347","NEWT:49928","NEWT:160621","NEWT:212790","NEWT:110368","NEWT:1310161","NEWT:77133","NEWT:145481","NEWT:1310165","NEWT:29058","NCBITaxon:79824","NEWT:410658","NEWT:5516","NEWT:44688","NEWT:44689","NEWT:498211","NEWT:347256","NEWT:5518","NEWT:398007","NEWT:1527468","NEWT:498217","NEWT:498216","NEWT:11320","NEWT:246196","NEWT:246197","NEWT:145458","NEWT:1310173","NEWT:44685","NEWT:161934","NEWT:156587","NEWT:1148","NEWT:5508","NEWT:3329","NEWT:419481","NEWT:5507","NEWT:410661","NEWT:1140","NCBITaxon:2157","NEWT:2066563","NEWT:1143","NEWT:1287689","NEWT:1094343","NEWT:1462472","NEWT:1336795","NEWT:644042","NEWT:150808","NEWT:1182590","NEWT:3712","NEWT:3711","NEWT:3714","NCBITaxon:37162","NEWT:270643","NEWT:2065263","NEWT:177437","NEWT:10891","NEWT:10418","NEWT:118698","NEWT:1616117","NEWT:118696","NEWT:34865","NEWT:52283","NEWT:28174","NEWT:284812","NEWT:8175","NEWT:43330","NEWT:1603293","NEWT:44664","NEWT:43346","NEWT:3702","NEWT:1245466","NEWT:3704","NEWT:244366","NEWT:1246791","NEWT:176597","NEWT:118694","NEWT:2850","NEWT:118691","NEWT:34871","NEWT:33548","NEWT:52299","NEWT:8165","NEWT:96794","NEWT:3708","NEWT:332648","NEWT:44670","NEWT:926571","NEWT:536231","NEWT:376219","NEWT:219813","NEWT:1510","NEWT:460519","NEWT:1515","NEWT:572307","NEWT:1432138","NEWT:1424507","NEWT:1194599","NEWT:272844","NEWT:1348799","NEWT:33995","NEWT:55784","NEWT:1303443","NEWT:9483","NEWT:485","NEWT:56636","NEWT:2499525","NEWT:2853422","NEWT:487","NEWT:1538553","NEWT:1679718","NEWT:480","NEWT:67767","NEWT:46835","NEWT:109757","NEWT:582580","NEWT:1185650","NEWT:216778","NEWT:294607","NEWT:1502","NEWT:128017","NEWT:376686","NEWT:237610","NEWT:95486","EFO:0001352","NEWT:119562","NEWT:1883446","NEWT:1233435","NEWT:118223","NEWT:11757","NEWT:987059","NEWT:109760","NEWT:29031","NEWT:317047","NEWT:1509","NEWT:491","NEWT:460523","NEWT:45954","NEWT:235443","NEWT:1579","NEWT:1757312","NEWT:85694","NEWT:109786","NEWT:108458","NEWT:5936","NEWT:320637","NEWT:1078283","NEWT:3750","NEWT:983964","NEWT:11706","NEWT:32644","NEWT:527796","NEWT:499175","NEWT:109779","NEWT:3745","NEWT:1715989","NCBITaxon:4751","NEWT:3747","NEWT:1116234","NEWT:1255228","NEWT:410289","NEWT:373153","NEWT:1640278","NEWT:472","NEWT:940825","NEWT:29459","NEWT:529507","NEWT:1071661","NEWT:28128","NEWT:470","NEWT:5911","NEWT:748693","NCBITaxon:50557","NEWT:39251","NEWT:29491","NEWT:101841","NEWT:446","NEWT:153481","NEWT:2014887","NEWT:33952","NEWT:11723","NEWT:445","NEWT:153009","NEWT:261756","NEWT:166313","NEWT:63366","NEWT:63367","NEWT:215402","NEWT:1547","NEWT:1290454","NEWT:906914","NEWT:28141","NEWT:9031","NEWT:27292","NEWT:1050722","NEWT:3728","NEWT:108931","NEWT:1293497","NEWT:1055524","NEWT:548","NEWT:150475","NEWT:267872","NEWT:381666","NEWT:172269","NEWT:9534","NEWT:2126348","NEWT:5180","NEWT:256737","NEWT:9541","NEWT:8694","NEWT:33936","NEWT:8692","NEWT:2903","NEWT:185579","NEWT:13076","NEWT:207340","NEWT:1006581","NEWT:8673","NEWT:33940","NEWT:550","NEWT:33941","NEWT:554","NEWT:451516","NEWT:552","NEWT:1325291","NEWT:42410","NEWT:36185","NEWT:1054211","NEWT:1225786","NEWT:771870","NEWT:51338","NEWT:9995","NEWT:575412","NEWT:28112","NEWT:49012","NEWT:6493","NEWT:10832","NEWT:6494","NEWT:6491","NEWT:507601","NEWT:520","NEWT:186441","NEWT:643680","NEWT:214092","NCBITaxon:6157","NEWT:13095","NEWT:162425","NEWT:104105","NEWT:216257","NEWT:9986","NEWT:8654","NEWT:8658","NEWT:1268063","NEWT:8657","NEWT:9983","NEWT:8655","NEWT:5147","NEWT:28108","NEWT:28104","NEWT:407821","NEWT:568703","NCBITaxon:2","NEWT:568708","NEWT:1613","NEWT:986","NEWT:52641","NEWT:28532","NEWT:353152","NEWT:298176","NEWT:353153","NEWT:227377","NEWT:1774284","NEWT:40674","NEWT:1194669","NEWT:51329","NEWT:74426","NEWT:443906","NEWT:13037","NEWT:519","NEWT:2510939","NEWT:7394","NEWT:6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