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Park"],"software":["Not available"],"tissue":["Blood Cell","Blood Plasma"],"sample_protocol":["(2) In-gel digestion of mIgA and dIgA serum antibodies. To determine IgA repertoires based on oligomeric states, 20 µg of serum IgA collected on day 29 post-vaccination was loaded in a 1.5 mm 3-8% NuPAGE tris-acetate gel (Thermo Scientific, cat# EA0378BOX) and separated based on molecular sizes by protein gel electrophoresis in a non-reducing, denaturing condition for 23–25 min at 200V. The LDS sample buffer (Thermo Fisher, cat# B0008) and MES SDS running buffer were used for electrophoresis (Thermo Fisher, cat# B000202), and HiMark pre-stained protein standard (Thermo Scientific, cat# LC5699) was used as a protein ladder. The following steps were performed inside the keratin-free laminar flow hoods. Gels were stained with instant Coomassie (Abcam, cat# ab119211) for 15 min and rinsed with HPLC-grade H2O (Fisher Scientific, cat# W6-1). Stained gels were transferred to sterile glass trays. Gel bands corresponding to the molecular sizes of dIgA (appear in the ladder of 330 – 360 kDa) and mIgA (appear in the ladder ~160 kDa) were excised using sterile blades (Fisher Scientific, cat# 12-460-441), cut into 1-2 mm cubes pieces, and collected in two separate protein low-binding tubes (Eppendorf, cat# 022431048) for mIgA and dIgA sample, respectively. Separate blades were used for mIgA and dIgA gel band cutting to prevent cross-contamination. Gel pieces were destained with 100 µl of destaining buffer (50% methanol, 5% acetic acid) in HPLC-grade H2O for 20 min. Supernatants were decanted, and the destaining step was repeated at least three times until gel pieces became fully transparent. Gel pieces were then dehydrated with 100 µl of 100% acetonitrile (Fisher Scientific, cat# A955-1) for 2–3 min. After removing excess acetonitrile, gel pieces were air-dried with lids open for 15–20 min inside the hood to remove any residual acetonitrile. For reduction of disulfide bonds, 100 µl of 10 mM DTT (Fisher Scientific, cat# AAJ1539706) dissolved in 100 mM ammonium bicarbonate (Sigma-Aldrich, cat# 09830-500G) was added to each sample and incubated for 1 hr at room temperature with shaking at 350 rpm in the dark. After removing DTT, alkylation was performed by incubating samples with 100 µl of 50 mM iodoacetamide (Sigma-Aldrich, cat# I1149-5G) dissolved in 100 mM ammonium bicarbonate for 1 hr at room temperature with shaking at 350 rpm in the dark. Gel pieces were then washed with 100 µl of 100 mM ammonium bicarbonate, vortexed, and incubated for 10 min. After three washes, samples were fully decanted and air-dried for 15 min. To perform in-gel tryptic digestion, 2 µl of 1 µg/ml Trypsin Gold (Promega, cat# V5280) stock, reconstituted in 50 mM acetic acid, was mixed with 100 µl of 50 mM ammonium bicarbonate, and the active trypsin solution was added to each sample and incubated on ice until gel pieces were fully hydrated. A few µl of 50 mM ammonium bicarbonate was added as needed to fully cover the gel pieces. Samples were digested overnight at 37°C with shaking. The following day, tubes were spun down to collect any condensation on the lid and incubated for an additional 1 hr at 37°C. To extract peptides, trypsin solution was decanted, and gel pieces were incubated with 100 µl of extraction buffer 1 containing 5% formic acid (Fisher Scientific, cat# A117-50) in HPLC-grade H2O, vortexed, centrifuged, and sonicated for 10–15 min. Supernatants were transferred to collection tubes. Gel pieces were then incubated with 100 µl of extraction buffer 2 (1:3 v/v of 5% formic acid with 100% acetonitrile), vortexed, centrifuged, and sonicated for an additional 10 min. The resulting supernatants were pooled into the same collection tube. To recover any remaining peptides from the gel pieces, a few µl of 100% acetonitrile was added to further dehydrate the gels, and the supernatants were combined into the collection tube. Extracted peptides were dried by speed vacuuming for 1.5–3 hr until 1-2 µl of buffer was left. Dried peptides were dissolved in 50 µl of 0.1 % formic acid and submitted to the UT Austin Center for Biomedical Research Support Biological Mass Spectrometry Facility (RRID: SCR_021728) with three technical replicates per sample on Thermo Ultimate 3000 RSLCnano UPLC and Orbitrap Fusion. The previously reported MS run method was used for raw data acquisition without modification66. The IgA and IgG mass exclusion lists are summarized in Table S11."],"repository":["Pride"],"labhead":["George Georgiou"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Department of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA"],"publication":["Not available"],"submitter_affiliation":["The University of Texas at Austin"],"labhead_mail":["gg@che.utexas.edu"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"disease":["Influenza"],"submitter_keywords":["Influenza","Monomeric iga","Antibodies","Dimeric iga"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD070307"],"quantification_method":[""],"modification":[""],"data_protocol":["Please refer to the published paper related to this work for the detailed data processing protocol. MS search workflow and CDRH3 peptide spectra-typing used in this study followed the previously reported method66,69, with a few modifications in which the isotype-specific MS databases were generated by appending “ASTK” for IgG or “ASPTSPK” for IgA at the 3’ end of the VH sequences. Briefly, CDRH3 peptide sequences were searched using the personalized isotype-specific MS database. Peptides that were detected with at least 2 peptide spectra matches (PSMs) across triplicate injections and that were unambiguously mapped to a single clonotype were sampled. For each sample, the abundance of individual clonotypes was quantified by summing the extracted ion chromatogram (XIC) peak areas of associated CDRH3 peptides mapped to a given clonotype. To identify antigen-specific IgG or IgA clonotypes, we first normalized the total XIC abundance of CDRH3 peptides detected in the elution and flowthrough fractions derived from the same affinity column and subsequently calculated the elution: flowthrough XIC ratio for each clonotype. Clonotypes identified with at least 5-fold higher XIC abundance in the elution compared to the flow-through in either day 1 or day 29 serum were defined as antigen-specific, as described previously43,66,69, and were included in downstream serum repertoire analyses. The relative abundance of each of the antigen-specific clonotypes was calculated by dividing the elution XIC of that clonotype by the total elution XIC summed across all antigen-specific clonotypes. To compare the abundance of each clonotype between two time points, the relative abundance values were further normalized using serum IgG or IgA ELISA titers at each time point, as reported previously43,66,69. This normalized metric is referred to as a relative amount in this study. For example, the relative amount of clonotypes on day 1 was calculated by dividing the day 1 relative abundance by the ratio of day 29 to day 1 serum ELISA titer. To analyze mIgA and dIgA repertoires, peptides (i) that were mapped to CDRH1, CDRH2, and CDRH3 regions of VH sequences with an average delta mass deviation < 5 ppm and (ii) that were uniquely assigned to a single clonotype were sampled for downstream analysis. To determine whether antigen-specific clonotypes (identified by affinity pull-down elution on day 29) were present in mIgA and/or dIgA form in day 29 serum, antigen-specific clonotype IDs and associated CDRH peptides were compared with those detected in the mIgA and dIgA samples."],"omics_type":["Proteomics"],"species":["Homo Sapiens (human)"],"submitter_mail":["juyeonpark@utexas.edu"],"curator_keywords":["Human proteome project","Biology/disease-driven human proteome project (b/d-hpp)","Antibodies (b/d-hpp)"],"submitter_country":["United States"],"additional_accession":[]},"is_claimable":false,"name":"Influenza serum mIgA and dIgA repertoire on day 29 following seasonal influenza vaccination","description":"Proteomic deconvolution of serum mIgA and dIgA repertoire specific to influenza HA following vaccination","dates":{"publication":"2026-07-09","submission":"2025-11-04"},"accession":"PXD070307","cross_references":{"TAXONOMY":["NEWT:330879","NEWT:377960","NEWT:1131","NEWT:35795","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:247480","NEWT:1211601","NEWT:876138","NEWT:44271","NEWT:193516","NEWT:2315688","NEWT:592321","NEWT:1073882","NEWT:6819","NEWT:475174","NEWT:111205","NEWT:1599","NEWT:428386","NEWT:1117","NEWT:498257","NEWT:10036","NEWT:32264","NEWT:12215","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:4615","NEWT:672127","NEWT:35786","NEWT:1580","NEWT:399784","NEWT:96731","NEWT:656064","NEWT:1582","NEWT:3760","NEWT:1584","NEWT:36630","NEWT:1585","NEWT:383379","NEWT:381198","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:3349","NEWT:160621","NEWT:212790","NEWT:110368","NEWT:55350","NEWT:1916073","NEWT:1310161","NEWT:77133","NEWT:145481","NEWT:1310165","NEWT:29058","NCBITaxon:79824","NEWT:1912919","NEWT:410658","NEWT:5516","NEWT:44688","NEWT:44689","NEWT:370038","NEWT:498211","NEWT:345076","NEWT:347256","NEWT:5518","NEWT:398007","NEWT:1527468","NEWT:498217","NEWT:498216","NEWT:11320","NEWT:246196","NEWT:246197","NEWT:145458","NEWT:1310173","NEWT:200795","NEWT:2579791","NEWT:44685","NEWT:161934","NEWT:156587","NEWT:1148","NEWT:5508","NEWT:3329","NEWT:419481","NEWT:5507","NEWT:260499","NEWT:410661","NEWT:329854","NEWT:1140","NCBITaxon:2157","NEWT:2066563","NEWT:2649329","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:3715","NEWT:1538","NEWT:2065263","NEWT:177437","NEWT:717966","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:9006","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:2709072","NEWT:2499525","NEWT:2853422","NEWT:487","NEWT:1538553","NEWT:1679718","NEWT:480","NEWT:67767","NEWT:45972","NEWT:46835","NEWT:109757","NEWT:582580","NEWT:1185650","NEWT:216778","NEWT:294607","NEWT:1502","NEWT:128017","NEWT:2836","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:85692","NEWT:321967","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:415978","NEWT:1255228","NEWT:410289","NEWT:191701","NEWT:373153","NEWT:1640278","NEWT:472","NEWT:940825","NEWT:29459","NEWT:529507","NEWT:1071661","NEWT:28128","NEWT:470","NEWT:41122","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:29488","NEWT:215402","NEWT:1547","NEWT:1290454","NEWT:3726","NEWT:906914","NEWT:81231006","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:542","NEWT:2903","NEWT:185579","NEWT:872227","NEWT:13076","NEWT:2587410","NEWT:207340","NEWT:1006581","NEWT:8673","NEWT:33940","NEWT:2126337","NEWT:550","NEWT:10804","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:28110","NEWT:6493","NEWT:10832","NEWT:6494","NEWT:6491","NEWT:507601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