{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19991_206_Cobo_CR_Peptide_5_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S20001_216_Cobo_CR_Peptide_15_260301.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19992_207_Cobo_CR_Peptide_6_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19995_210_Cobo_CR_Peptide_9_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19990_205_Cobo_CR_Peptide_4_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19997_212_Cobo_CR_Peptide_11_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S20002_217_Cobo_CR_Peptide_16_260301.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19999_214_Cobo_CR_Peptide_13_260301.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19994_209_Cobo_CR_Peptide_8_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S20000_215_Cobo_CR_Peptide_14_260301.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19993_208_Cobo_CR_Peptide_7_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19988_203_Cobo_CR_Peptide_2_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19998_213_Cobo_CR_Peptide_12_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19989_204_Cobo_CR_Peptide_3_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19987_202_Cobo_CR_Peptide_1_260228.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/S19996_211_Cobo_CR_Peptide_10_260228.raw"],"Other":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD076043/2026-3-6_Cobo_CR_peptide.zip"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["Antoine.dufour@ucalgary.ca"],"submitter":["Daniel Young"],"technology_type":["Mass Spectrometry","Data-independent acquisition","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Host defence peptides; colitis; citrobacter rodentium.","colitis","citrobacter rodentium.","Host defence peptides"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD076043"],"tissue":["Colon"],"sample_protocol":["The shotgun proteomic analysis was performed as described previously  (10),. Briefly, tissue samples here bead bater homogenized. a small tissue samples was mixed with 500 ul of lysis buffer (1% SDS, 50 mM Amonium bicarbonate and protease inhibitor) with 3 stainless steal beads followzed by bead beating at 30 hz for 20 minutes using a Qiagen tissuelyser 2. Samples we centrifuged at 14 000 xg for 10 minutes to pellet unwanted debris. BCA quantification was performed on the supenatient according th manufacters directions (thermofisher)  Samples were prepared using the filter-assisted separation of peptides (FASP) method4. 100 ug of protein was precipitated by adding trichloroacetic acid (TCA, 25% v/v final) followed by an incubation on ice. Samples were then centrifuged at 14,000 xg for 15 minutes at 4°C, washed 3 times in ice cold acetone, and stored at -20°C overnight. Samples were resuspended in 8M tris-urea solution by shaking and then denatured with the addition of 10 mM DTT at 37°C for 30 minutes. Samples were moved to the top of a 30 kDa filter and were then centrifuged at 14,000 x g for 15 minutes.  50 mM iodoacetamide was added in the dark at room temperature to complete carbamidomethyl modification of the cystines. Samples were then washed 3 times with 100 ul of 8 M tris-urea and 3 times with followed by 3 washes in 100 ul of 50 mM ammonium bicarbonate. The samples were trypsinized at 37°C overnight at a ratio of 1:10 trypsin: total protein, and subsequently, eluted off the filter membrane by washing two times with 50 mM ammonium bicarbonate. Finally, samples were subjected to a c18 clean up with waters solid-phase extraction (SPE) column, according to directions from the manufacturer. High performance liquid chromatography (HPLC) and mass spectrometry (MS)  Tryptic peptides were analyzed on an Orbitrap Fusion Lumos Tribrid mass spectrometer (Thermo Scientific) operated with Xcalibur (version 4.4.16.14) and coupled to a Thermo Scientific Easy-nLC (nanoflow Liquid Chromatography) 1200 system. A total mass of 2 μg tryptic peptides were loaded onto a C18 trap (75 um x 2 cm; Acclaim PepMap 100, P/N 164946; ThermoScientific) at a flow rate of 2ul/min of solvent A (0.1% formic acid in LC-MS grade water). Peptides were eluted using a 120 min gradient from 5 to 40% (5% to 28% in 105 min followed by an increase to 40% B in 15 min) of solvent B (0.1% formic acid in 80% LC-MS grade acetonitrile) at a flow rate of 0.3 μL/min and separated on a C18 analytical column (75 um x 50 cm; PepMap RSLC C18; P/N ES803; ThermoScientific). The mass spec was opetated in DIA mode using the default settings from the manufacturer. Peptides were then electrosprayed using 2.1 kV voltage into the ion transfer tube (300°C) of the Orbitrap Lumos operating in positive mode. The Orbitrap first performed a full MS scan at a resolution of 120000 FWHM to detect the precursor ion having a m/z between 380 and 985 and a +2 to +7 charge. The Orbitrap AGC (Auto Gain Control) and the maximum injection time were set at standard and 50 ms, respectively. The Orbitrap was operated using the top speed mode with a 3 sec cycle time for precursor selection. The fragment ions (MS2) were analyzed in the orbitrap with a 40 sliding windows of 16.0072 m/z starting at 379.4224. The precurson ions within the sliding windows were sleected for MS2 with HCD (30% collision energy) in the ion routing multipole. The AGC and the maximum injection time were set at 1e4 and 35 ms, respectively, for the quadrupole."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["Spectra data obtained during mass-spectrometry were matched to peptide sequences from a mouse reference file obtained from Uniprot on March 20th, 2024, using DIA-NN (v.1.8.1). DIANN was run in “FASTA digest for library -free search mode” Variable modifications included N-term M excisions. Fixed modifications included Carbamidomethylation on Cystines.  All other DIANN settings were set to default1. MSstatsShiny UI (v0.1.0; https://msstatsshiny.com/app/MSstatsShiny) running MSstats (v.4.2.0) was used to run the statistical analysis2. The DIANN file “Report.tsv” were used for the analysis, while the annotation file was created according to directions provided by MSstats. Unique peptides were included in the analysis. For data processing, log2 was defined for data transformation and equalize medians was the method chosen for normalization. The options that were enabled for this analysis were “Use unique peptides”, “remove proteins with 1 feature”, and “remove runs with over 50% missing values”. Statistical inference was performed using custom pairwise comparisons, and the data was imported to excel for final assessment. Significant enriched proteins for each group were found using a p-value cut-off of 0.05. Metascape analysis was used to identify enriched pathways3. Protein-protein interactions were encoded into networks using the metascape website (https://metascape.org/), and enriched pathways were plotted as heatmaps."],"omics_type":["Proteomics"],"labhead":["Antoine Dufour"],"instrument_platform":[""],"labhead_affiliation":["Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta, T2N 4N1, Canada."],"submission_type":["PARTIAL"],"species":["Mus Musculus (mouse)"],"submitter_mail":["daniel.young1@ucalgary.ca"],"publication":["Not available"],"submitter_affiliation":["University of Calgary"],"submitter_country":["Canada"],"additional_accession":[]},"is_claimable":false,"name":"Cathelicidin derivative IDR-1018 exhibits anti-protease effects that alleviate Citrobacter rodentium-induced colitis","description":"Short, cationic, and amphipathic host defence peptides exhibit a wide range of anti-infective, anti-inflammatory, wound-healing, and antibiofilm activities. A synthetic peptide innate defence regulator (IDR) 1018, derived from the bovine neutrophil bactenecin, has been proposed as a therapeutic candidate for treating bacterial infections due to its immunomodulatory and antibacterial properties. IDR-1018 was examined as a treatment in murine colitis caused by the attaching/effacing enteropathogen, Citrobacter rodentium. IDR-1018, administered intra-peritoneally for three consecutive days after oral challenge with C. rodentium, mitigated microscopic lesions of colitis. Specifically, IDR-1018 reduced fecal protease levels, particularly elastase, by increasing the formation of inhibitory elastase–serpin complexes. IDR-1018 targeted neutrophils, the main effectors in colitis. Human and murine neutrophils stimulated and recruited by IDR-1018 exhibited reduced protease and elastase activity, as well as lower inflammatory cytokine production in response to inflammatory stimulation, showing functional reprogramming toward a less tissue-damaging phenotype. This study reveals a new activity of IDR-1018 in counteracting protease, which correspondingly attenuates C. rodentium colitis.","dates":{"publication":"2026-04-14","submission":"2026-03-24"},"accession":"PXD076043","cross_references":{"TAXONOMY":["NEWT:108018","NEWT:377960","NEWT:1131","NEWT:190486","NEWT:2042546","NEWT:148942","NEWT:295546","NEWT:258594","NEWT:1126","NEWT:1129","NEWT:89187","NEWT:309807","NEWT:89184","NEWT:309800","NEWT:1323429","NEWT:876138","NEWT:44271","NEWT:193516","NEWT:2315688","NEWT:592321","NEWT:1073882","NEWT:6819","NEWT:428386","NEWT:1117","NEWT:498257","NEWT:10036","NEWT:32264","NEWT:10034","NEWT:661410","NEWT:488003","NEWT:224326","NEWT:376619","NEWT:3765","NEWT:3767","NEWT:433727","NEWT:135622","NEWT:672127","NEWT:656061","NEWT:37965","NEWT:656064","NEWT:3760","NEWT:36630","NEWT:381198","NEWT:418106","NEWT:10029","NEWT:913645","NEWT:641809","NEWT:44250","NEWT:317447","NEWT:5530","NEWT:868565","NEWT:135674","NEWT:1562698","NEWT:12637","NEWT:2164133","NEWT:2767846","NEWT:1343074","NEWT:314344","NEWT:108061","NEWT:224308","NEWT:49928","NEWT:160621","NEWT:110368","NEWT:1916073","NEWT:1310161","NEWT:1230383","NEWT:77133","NEWT:1310165","NEWT:114727","NEWT:5516","NEWT:498211","NEWT:347256","NEWT:5518","NEWT:398007","NEWT:1527468","NEWT:498217","NEWT:498216","NEWT:11320","NEWT:1310173","NEWT:161934","NEWT:1148","NEWT:5508","NEWT:419481","NEWT:5507","NEWT:1140","NCBITaxon:2157","NEWT:2066563","NEWT:1143","NEWT:1462472","NEWT:1336795","NEWT:644042","NEWT:709964","NEWT:3712","NEWT:3711","NEWT:3714","NEWT:65121","NEWT:3715","NEWT:2065263","NEWT:1549675","NEWT:177437","NEWT:9014","NEWT:10891","NEWT:118221","NEWT:34869","NEWT:226126","NEWT:1616117","NEWT:34865","NEWT:550537","NEWT:284812","NEWT:3701","NEWT:3702","NEWT:1245466","NEWT:3704","NEWT:1246791","NEWT:34875","NEWT:9005","NEWT:34871","NEWT:9006","NEWT:33548","NEWT:1883426","NEWT:657321","NEWT:10886","NEWT:3708","NEWT:536231","NEWT:219813","NEWT:215451","NEWT:460519","NEWT:272843","NEWT:272844","NEWT:1348799","NEWT:55784","NEWT:485","NEWT:2499525","NEWT:467144","NEWT:142786","NEWT:2853422","NEWT:487","NEWT:1679718","NEWT:480","NEWT:67767","NEWT:46835","NEWT:216778","NEWT:376686","NEWT:237610","EFO:0001352","NEWT:219809","NEWT:219808","NEWT:119562","NEWT:1883446","NEWT:1233435","NEWT:118223","NEWT:141469","NEWT:272831","NEWT:987059","NEWT:491","NEWT:460523","NEWT:2423","NEWT:85694","NEWT:85692","NEWT:911045","NEWT:3750","NEWT:291146","NEWT:233271","NEWT:3745","NEWT:1715989","NCBITaxon:4751","NEWT:3747","NEWT:278161","NEWT:415978","NEWT:410289","NEWT:191701","NEWT:9054","NEWT:472","NEWT:29459","NEWT:28128","NEWT:470","NEWT:41122","NEWT:1328300","NEWT:748693","NCBITaxon:50557","NEWT:3735","NEWT:29491","NEWT:911022","NEWT:446","NEWT:153481","NEWT:714485","NEWT:445","NEWT:2003758","NEWT:63366","NEWT:63367","NEWT:29488","NEWT:215402","NEWT:3726","NEWT:30455","NEWT:28141","NEWT:9030","NEWT:9031","NEWT:3728","NEWT:108931","NEWT:219799","NEWT:1325292","NEWT:219798","NEWT:548","NEWT:150475","NEWT:256737","NEWT:51350","NEWT:8694","NEWT:8692","NEWT:542","NEWT:394503","NEWT:13076","NEWT:219785","NEWT:451515","NEWT:8673","NEWT:550","NEWT:10804","NEWT:554","NEWT:451516","NEWT:552","NEWT:1325291","NEWT:42410","NEWT:1225786","NEWT:771870","NEWT:8665","NEWT:51338","NEWT:9995","NEWT:28112","NEWT:49012","NEWT:28110","NEWT:10832","NEWT:311339","NEWT:507601","NEWT:520","NEWT:64657","NEWT:186441","NEWT:2585209","NEWT:643680","NEWT:214092","NEWT:40697","NEWT:13095","NEWT:162425","NEWT:242124","NEWT:9986","NEWT:8654","NEWT:8658","NEWT:1268063","NEWT:8657","NEWT:9983","NEWT:8655","NEWT:80833","NEWT:479096","NEWT:28108","NEWT:28104","NEWT:1114957","NEWT:568703","NEWT:568708","NEWT:52641","NEWT:353152","NEWT:353153","NEWT:227377","NEWT:1774284","NEWT:27689","NEWT:207769","NEWT:40674","NEWT:51329","NCBITaxon:1763","NEWT:443906","NEWT:13037","NEWT:519","NEWT:941638","NEWT:7394","NEWT:6063","NEWT:404330","NEWT:1328388","NEWT:13064","NEWT:300641","NEWT:39655","NEWT:206411","NEWT:80869","NEWT:214053","NEWT:80863","NEWT:665890","NEWT:52639","NEWT:52638","NEWT:8697","NEWT:861109","NEWT:8695","NEWT:1196866","NEWT:6039","NEWT:1045775","NEWT:1123869","NCBITaxon:1335626","NEWT:7370","NEWT:280406","NEWT:83906","NEWT:99488","NEWT:1134506","NEWT:255470","NEWT:762903","NEWT:27697","NEWT:86185","NEWT:9935","NEWT:266940","NEWT:287889","NEWT:1028307","NEWT:52603","NEWT:92867","NEWT:92866","NEWT:1344414","NEWT:202950","NEWT:741158","NEWT:1293091","NEWT:202956","NEWT:483179","NEWT:315750","NEWT:632957","NEWT:9925","NCBITaxon:9606","NEWT:1436183","NEWT:1479235","NEWT:4232","NEWT:9922","NEWT:416348","NEWT:105812","NEWT:11298","NEWT:4233","NEWT:4236","NEWT:398031","NEWT:196627","NEWT:523840","NEWT:1076878","NEWT:200308","NEWT:200302","NEWT:9913","NEWT:9915","NEWT:105841","NEWT:1170227","NEWT:2666255","NEWT:999810","NEWT:28995","NEWT:1392998","NEWT:1150621","NEWT:1085791","NEWT:745531","NEWT:226900","NEWT:231490","NEWT:590651","NEWT:449239","NEWT:244704","NEWT:9909","NEWT:9902","NEWT:430615","NEWT:563041","NEWT:36599","NEWT:41949","NEWT:9900","NEWT:326423","NEWT:326424","NEWT:13013","NEWT:749906","NE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