{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Tabular":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/20250512_085413_029_2024_DUN_HM_directDIA_mouse_hpoly_cont_normalised_contrasts_v19_protein_pivot_Report.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_DUN_HM_directDIA_mouse_hpoly_cont_normalised_contrasts_v19_ConditionSetup.tsv"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/checksum.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/Hpolyin_houseTranscriptomen143104_DUPESREMOVED.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_11.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_8.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_13.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_15.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_6.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_10.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_12.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_14.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_9.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_5.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_7.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/029_2024_NO_16.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/0602_Universal_Contaminants.fasta","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/04/PXD074451/mouse_swiss_trembl_nov_23.fasta"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["hmcsorley001@dundee.ac.uk"],"submitter":["Andrew Howden"],"technology_type":["Mass Spectrometry","Bottom-up proteomics","Data-independent acquisition"],"software":[""],"submitter_keywords":["st2","il-33","proteomics","Interleukin-33","mast cell","transcriptomics","heligmosomoides polygyrus bakeri","Interleukin-33; il-33; st2; mast cell; heligmosomoides polygyrus bakeri;  proteomics; transcriptomics"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD074451"],"tissue":["Small Intestine"],"sample_protocol":["Sample Preparation for Mass Spectrometry  Subsequent 0.5 cm of small intestine from the duodenum end was dissected, flash   frozen in dry ice and stored at -70oC until processing for mass spectrometry. Sample  preparation protocol was adapted from published literature (Baker et al., 2022). Briefly,  tissue was digested in lysis buffer (5% SDS, 50mM TEAB in water) and sonicated at  maximum amplitude for 15 cycles of 30 seconds on, 30 seconds off. Tubes were briefly  centrifuged to collect liquid to bottom of tubes, and benzonase (Merck) added. Protein  yield was determined using BCA method, then TCEP (final concentration 10 mM) added  and incubated at 55oC for 5 min. 0.5M iodoacetamide (Sigma) was added to samples and  incubated at room temperature for 1 hour in the dark. Lysates were acidified and loaded  onto S-Trap™ mini spin columns (ProtiFi) for trypsin (Promega) digestion and peptide  dehydration as described previously (Baker et al., 2022). A sample of excretory/secretory  products of Hpb (HES – prepared as previously described (Johnston et al., 2015)) was  also prepared and run for proteomic analysis and comparison.   Liquid Chromatography-Mass Spectrometry (LC-MS) Mass spectrometry was conducted by University of Dundee FingerPrints Proteomics  Facility. Sample volumes equivalent to 1.25 µg of peptides were injected onto an  UltiMate™ 3000 RSLCnano system (Thermo Scientific) and electrosprayed into an  Orbitrap Exploris 480 Mass Spectrometer (Thermo Fisher). The following LC buffers were  used: Buffer A - 0.1% formic acid (Fisher Scientific) in MilliQ water (v/v)); Buffer B - 80%  acetonitrile (VWR) and 0.1% formic acid in MilliQ water (v/v). Samples were loaded at 10  µl/minute onto a trap column (100 µm x 2 cm, PepMap nanoViper C18 column, 5 µm, 100  Å, Thermo Scientific) equilibrated with 0.1% trifluoroacetic acid (TFA, Thermo Scientific).  The trap column was washed for 3 minutes at the same flow rate with 0.1% TFA then  switched in-line with a resolving C18 column (75 μm × 50 cm, PepMap RSLC C18 column,  2 μm, 100 Å, Thermo Scientific). Peptides were eluted from the column at a constant flow  rate of 300 nl/min with a linear gradient from 3% buffer B to 6% buffer B in 5 minutes, then  from 6% buffer B to 35% buffer B in 115 minutes, and finally from 35% buffer B to 80%  buffer B within 7 minutes. The column was then washed with 80% buffer B for 4 minutes.  Two blanks were run between each sample to reduce carry-over. The column was kept  at a temperature of 50 °C. The data was acquired using an easy spray source operated in positive mode with spray  voltage at 2.25 kV, and the ion transfer tube temperature at 250 °C. The MS was operated  in DIA mode. A scan cycle comprised a full MS scan (m/z range from 350-1650), with RF  lens at 40%, AGC target set to custom, normalised AGC target at 300%, maximum  injection time mode set to custom, maximum injection time at 20 ms, microscan set to  1 and source fragmentation disabled. MS survey scan was followed by MS/MS DIA scan  events using the following parameters: multiplex ions set to false, collision energy type  set to normalized, HCD collision energies set to 25.5, 27 and 30%, orbitrap resolution  30000, first mass 200, RF lens 40%, AGC target set to custom, normalized AGC target  3000%, microscan set to 1 and maximum injection time 55 ms. Loop control N, N  (number of spectra set to 23). Data for both MS scan and MS/MS DIA scan events were  acquired in profile mode."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["Proteomic Analysis Raw data files were ran on Spectronaut 19 against Mus musculus (Swissprot Trembl  November 2023), Hpb (transcriptome described previously (Hewitson et al., 2011)) and  common contaminants fasta file using stringent identification settings (Baker et al.,  164 2024). Intensity-based absolute quantification (iBAQ) was exported from Spectronaut  and used for quantitative analysis. M. musculus and Hpb proteomes were separated,  and differential comparisons were conducted using limma function outputs including  log2 fold changes, p-values, and q-values (Ritchie et al., 2015). Hpb proteins were  analysed for the presence of a signal peptide using SignalP - 6.0 (Teufel et al., 2022)."],"omics_type":["Proteomics"],"labhead":["Henry McSorley"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["University of Dundee"],"species":["Mus Musculus (mouse)"],"publication":["41906940 Ong NWP, Hodge SH, Baker CP, Smyth DJ, Frangova T, McSorley HJ. Transcriptomic and Proteomic Analyses Show Minimal Role for ST2 on MCPT5-Expressing Mast Cells in Primary Heligmosomoides polygyrus bakeri Infection. Parasite Immunol. 2026 48(4):e70076 10.1111/pim.70076"],"submitter_mail":["a.howden@dundee.ac.uk"],"submitter_affiliation":["University of Dundee"],"submitter_country":["United Kingdom"],"pubmed_abstract":["The IL-33/ST2 pathway is important as part of the type 2 immune response against helminth infections. Mast cells express the highest levels of the IL-33 receptor subunit ST2 of any immune cell, and mast cells can mediate type 2 immune inflammation; however, the role of IL-33-driven mast cell responses in helminth infection is poorly understood. We sought to determine the role of mast cell ST2 expression during Heligmosomoides polygyrus bakeri (Hpb) infection by generating mast cell conditional ST2 knockout (MCPT5<sup>Cre</sup> × ST2<sup>f/f</sup>, cKO) mice. These mice have normal frequencies of mast cells at steady state but show specific and strong (albeit incomplete) knockdown of ST2 expression on mast cells. On Hpb infection, faecal egg and adult worm burden were similar between cKO and littermate controls, as were mast cell degranulation markers, serum IgE and goblet cell hyperplasia. Therefore, we conclude that mast cell ST2 does not play a dominant role in Hpb infection. To further investigate the immune response to infection in cKO and littermate controls, transcriptomic and proteomic changes were assessed in duodenal tissues in infected versus naïve mice in cKO and control mice. Minimal transcriptomic and proteomic changes were seen between genotypes, whereas substantial changes were seen between naïve and infected mice, regardless of genotype. Hpb infection induced local increases at the transcript and protein level for mast cell proteases (MCPT1 and MCPT2), resistin-like molecules (RELMα and RELMβ) and markers such as the phospholipase PLA2G4C and the pore-forming protein gasdermin C. Bulk proteomic analysis was also searched against the Hpb genome to identify Hpb proteins present in the duodenal tissues. A list of 60 Hpb proteins of interest was identified in infected duodenal samples, of which 18 contain a signal peptide and are present in the excretory/secretory products of Hpb (HES) (likely secretory products including immunomodulatory proteins); 28 proteins are present in HES but do not contain a signal peptide (likely excretory products); and 14 proteins are not present in HES (likely proteins present in the remnants of Hpb within the duodenum). This work thus provides datasets for changes in the mouse intestine due to Hpb infection, at both the transcript and protein level, as well as a dataset of Hpb proteins detectable in the mouse duodenum at day 14 of infection."],"pubmed_title":["Transcriptomic and Proteomic Analyses Show Minimal Role for ST2 on MCPT5-Expressing Mast Cells in Primary Heligmosomoides polygyrus bakeri Infection."],"pubmed_authors":["Ong Nicole W P NWP, Hodge Suzanne H SH, Baker Christa P CP, Smyth Danielle J DJ, Frangova Tania T, McSorley Henry J HJ"],"additional_accession":[]},"is_claimable":false,"name":"Transcriptomic and proteomic analyses show minimal role for  mast cell ST2 in primary Heligmosomoides polygyrus bakeri  infection","description":"The IL-33/ST2 pathway is important as part of the type 2 immune response against  helminth infections. Mast cells express the highest levels of the IL-33 receptor subunit  ST2 of any immune cell, and mast cells can mediate type 2 immune inflammation,  however the role of IL-33-driven mast cell responses in helminth infection is poorly  understood. We sought to determine the role of mast cell ST2 expression during  Heligmosomoides polygyrus bakeri (Hpb) infection by generating mast cell conditional  ST2 knockout (MCPT5Cre x ST2f/f ,cKO) mice. These mice have normal frequencies of mast  cells at steady state, but show specific and strong (albeit incomplete) knockdown of ST2  expression on mast cells. On Hpb infection, faecal egg and adult worm burden were  similar between cKO and littermate controls, as were mast cell degranulation markers,  serum IgE and goblet cell hyperplasia. Therefore, we conclude that mast cell ST2 does  not play a dominant role in Hpb infection. To further investigate the immune response to  infection in cKO and littermate controls, transcriptomic and proteomic changes were  assessed in duodenal tissues in infected versus naïve mice in cKO and control mice.  Minimal transcriptomic and proteomic changes were seen between genotypes, whereas  substantial changes were seen between naïve and infected mice, regardless of  genotype. Hpb infection induced local increases at the transcript and protein level for  mast cell proteases (MCPT1 and MCPT2), resistin-like molecules (RELMα and RELMβ), and markers such as the phospholipase PLA2G4C and the pore-forming protein  gasdermin C. Bulk proteomic analysis was also searched against the Hpb genome to  identify Hpb proteins present in the duodenal tissues. A list of 60 Hpb proteins of interest  were identified in infected duodenal samples, of which 18 contain a signal peptide and  are present in the excretory/secretory products of Hpb (HES) (likely secretory products  including immunomodulatory proteins); 28 proteins are present in HES but do not  contain a signal peptide (likely excretory products); and 14 proteins are not present in  HES (likely proteins present in the remnants of Hpb within the duodenum). This work thus  provides datasets for changes in the mouse intestine due to Hpb infection, at both the  transcript and protein level, as well as a dataset of Hpb proteins detectable in the mouse  duodenum at day 14 of infection.","dates":{"publication":"2026-04-06","submission":"2026-02-13"},"accession":"PXD074451","cross_references":{"TAXONOMY":["NEWT:108018","NEWT:377960","NEWT:1131","NEWT:190486","NEWT:2042546","NEWT:148942","NEWT:295546","NEWT:258594","NEWT:1126","NEWT:1129","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: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: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:226126","NEWT:1616117","NEWT:34865","NEWT:550537","NEWT:284812","NEWT:3701","NEWT:3702","NEWT:1245466","NEWT:3704","NEWT:1246791","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:272844","NEWT:1348799","NEWT:55784","NEWT:485","NEWT:2499525","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: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: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: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: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","NCBITaxon:1763","NEWT:443906","NEWT:13037","NEWT:519","NEWT:7394","NEWT:6063","NEWT:404330","NEWT:1328388","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:83906","NEWT:99488","NEWT:1134506","NEWT:255470","NEWT:27697","NEWT:86185","NEWT:9935","NEWT:287889","NEWT:1028307","NEWT:52603","NEWT:92867","NEWT:92866","NEWT:1344414","NEWT:202950","NEWT:741158","NEWT:1293091","NEWT:202956","NEWT:315750","NEWT:632957","NEWT:9925","NCBITaxon:9606","NEWT:1436183","NEWT:4232","NEWT:9922","NEWT:416348","NEWT:105812","NEWT:11298","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","NEWT:418985","NEWT:749907","NEWT:431947","NEWT:142809","NEWT:1095183","NEWT:302409","NEWT:9979","NEWT:130821","NEWT:2320211","NEWT:27606","NEWT:290610","NEWT:1519788","NEWT:59202","NEWT:9975","NEWT:8643","NEWT:1801631","NEWT:1159899","NEWT:502780","NEWT:860688","NEWT:35231","NEWT:1774208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