{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Xlsx":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_perseus_quant_file.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_VWRSolvVWREDL_perseus_quant_file.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_Soleus_perseus_quant_file.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_SedSolvsSedEDL_perseus_quant_file.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_SedSolvsSedEDL_perseus_quant_file.xlsx","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_EDL_perseus_quant_file.xlsx"],"Tabular":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_diann_search_file.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_diann_report_generator_quant_file.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_diann_search_file.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_mbr_library.tsv.speclib","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_diann_report_generator_quant_file.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_mbr_library.tsv.speclib"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/checksum.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTS2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSV1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSS1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTV-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTS-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTV3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSS-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSV-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTS-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSV-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTV-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSS-2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSV3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTV-1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSS3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSV-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSV2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTS3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTS1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_GSS-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTV1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_GSS2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/lumos_WTS-3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/astral_WTV2.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/08/PXD082130/mouse_one-protein-per-gene_fasta.fasta"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"labhead_mail":["Robert_Dirksen@URMC.Rochester.edu"],"submitter":["Kyle Swovick"],"technology_type":["Mass Spectrometry","Bottom-up proteomics","Data-independent acquisition"],"software":[""],"submitter_keywords":["Mitochondria","Exercise","Sarcoplasmic reticulum","Proteomics","Physiology","Aggregate","Skeletal muscle","Myopathy"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD082130"],"tissue":["Skeletal Muscle"],"sample_protocol":["Whole soleus and EDL muscles from male mice were flash-frozen in liquid nitrogen and stored at −80 °C until ready for use. Samples were homogenized in 250 µL of 5% SDS, 100 mM TEAB and sonicated (QSonica, Newtown, CT, USA) for 5 cycles with 1 min incubation on ice after each cycle. Samples were then centrifuged at 15,000× g for 5 min to collect the supernatant. A bicinchoninic (BCA) assay (Thermo Fisher, Carlsbad, CA, USA) was used for protein quantitation. Samples were diluted to 1 mg/mL in 5% SDS, 50 mM TEAB. 25 µg of protein from each sample was reduced with dithiothreitol (2 mM) and incubated at 55 °C for 1 h. Iodoacetamide (10 mM) was then added and samples were incubated at RT for 30 min in the dark to alkylate proteins. Phosphoric acid (1.2%) was added, followed by six volumes of 90% methanol, 100 mM TEAB. Samples were added to S-Trap micros (Protifi, Fairport, NY, USA), and centrifuged at 4000× g for 1 min. S-Traps were washed twice by centrifuging through 90% methanol, 100 mM TEAB. 20 µL of 100 mM TEAB with 1 µg trypsin added to the S-Trap, followed by an additional 20 µL of TEAB. Samples were incubated at 37 °C overnight. S-Traps were centrifuged at 4000× g for 1 min to collect the digested peptides. Sequential additions of 0.1% trifluoroacetic acid (TFA) in 50% acetonitrile were added to the S-trap, centrifuged, and pooled. Samples were frozen and dried in a Speed Vac (Labconco, Kansas City, MO, USA) and resuspended in 0.1% TFA prior to mass spectrometry analysis. Peptides were injected onto 30 cm C18 columns with 1.8 μm beads (Sepax, Newark, DE, USA) on an Easy nLC-1200 HPLC (Thermo Fisher, Carlsbad, CA, USA) connected to a Fusion Lumos Tribrid mass spectrometer (Thermo Fisher, Carlsbad, CA, USA) operating in data-independent mode. Ions were introduced to the mass spectrometer using a Nanospray Flex source operating at 2 kV. The gradient proceeded as 3% solvent B (0.1% formic acid in 80% acetonitrile) for 2 min, 10% solvent B for 6 min, 38% solvent B for 65 min, 90% solvent B for 5 min, held for 3 min, returned to starting conditions for 2 min and re-equilibrated for 7 min. The full MS1 scan was conducted from 395–1005 m/z, with a resolution of 60,000 at m/z of 200, an AGC target of 4 × 105 and a maximum injection time of 50 ms. MS2 scans were performed by using higher energy dissociation with a staggered windowing scheme of 14 m/z with 7 m/z overlaps, with fragment ions analyzed in the Orbitrap with a resolution of 15,000, an automatic gain control (AGC) target of 4 × 105 and a maximum injection time of 23 ms."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["Raw data was processed using DIA-NN version 1.8.1 (https://github.com/vdemichev/DiaNN, accessed on 1 July 2022) in library-free analysis mode [64]. Library annotation was conducted using the mouse UniProt ‘one protein sequence per gene’ database (UP000000589_10090) with deep learning-based spectra and RT prediction enabled. For precursor ion generation, the maximum number of missed cleavages was set to 1, maximum number of variable modifications set to 1 for Ox(M), peptide length range set to 7–30, precursor charge range set to 2–3, precursor m/z range set to 400–1000, and fragment m/z range set to 200–2000. Quantification was set to ‘Robust LC (high precision)’ mode with cross-run normalization set to RT-dependent, MBR enabled, protein inferences set to ‘Genes’, and ‘Heuristic protein inference’ turned off. MS1 and MS2 mass tolerance and scan window size were automatically set by the software. Precursors were subsequently filtered at library precursor q-value (1%), library protein group q-value (1%), and posterior error probability (50%). Protein quantification was carried out using the MaxLFQ algorithm implemented in the DIA-NN R package. Peptide number was quantified in each protein group and implemented in the DiannReportGenerator package (https://github.com/URMC-MSRL/DiannReportGenerator, accessed on 1 July 2022) [65]. Only significantly different (p < 0.05) proteins within the top three quartiles of mean peptide abundance were included in analysis. Individual group comparison pathway and network analyses were conducted using ShinyGO 0.77 (South Dakota State University, Brookings, SD, USA) [66,67,68]. The top ten identified pathways were extracted from Gene Ontology (GO) Biological Process, GO Cellular Component, and KEGG pathway databases. The false discovery rate (FDR) cutoff was set at 0.05 and pathways were sorted by −Log10(FDR)."],"omics_type":["Proteomics"],"labhead":["Robert T. Dirksen"],"instrument_platform":[""],"submission_type":["PARTIAL"],"labhead_affiliation":["Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY 14642, USA"],"species":["Mus Musculus (mouse)"],"submitter_mail":["kswovick@ur.rochester.edu"],"publication":["40940794 O'Connor TN, Zhao N, Orciuoli HM, Malik S, Brasile A, Pietrangelo L, He M, Groom L, Leigh J, Mahamed Z, Liang C, Protasi F, Dirksen RT. Voluntary Wheel Running Mitigates Disease in an Orai1 Gain-of-Function Mouse Model of Tubular Aggregate Myopathy. Cells. 2025 14(17):1383 10.3390/cells14171383","10.3390/CELLS14171383"],"submitter_affiliation":["University of Rochester Medical Center Mass Spectrometry Shared Resource Laboratory"],"submitter_country":["United States"],"pubmed_abstract":["Tubular aggregate myopathy (TAM) is an inherited skeletal muscle disease associated with progressive muscle weakness, cramps, and myalgia. Tubular aggregates (TAs) are regular arrays of highly ordered and densely packed straight-tubules observed in muscle biopsies; the extensive presence of TAs represent a key histopathological hallmark of this disease in TAM patients. TAM is caused by gain-of-function mutations in proteins that coordinate store-operated Ca<sup>2+</sup> entry (SOCE): STIM1 Ca<sup>2+</sup> sensor proteins in the sarcoplasmic reticulum (SR) and Ca<sup>2+</sup>-permeable ORAI1 channels in the surface membrane. Here, we assessed the therapeutic potential of endurance exercise in the form of voluntary wheel running (VWR) in mitigating TAs and muscle weakness in <i>Orai1<sup>G100S/+</sup></i> (GS) mice harboring a gain-of-function mutation in the ORAI1 pore. Six months of VWR exercise significantly increased specific force production, upregulated biosynthetic and protein translation pathways, and normalized both mitochondrial protein expression and morphology in the <i>soleus</i> of GS mice. VWR also restored Ca<sup>2+</sup> store content, reduced the incidence of TAs, and normalized pathways involving the formation of supramolecular complexes in fast twitch muscles of GS mice. In summary, sustained voluntary endurance exercise improved multiple skeletal muscle phenotypes observed in the GS mouse model of TAM."],"pubmed_title":["Voluntary Wheel Running Mitigates Disease in an Orai1 Gain-of-Function Mouse Model of Tubular Aggregate Myopathy."],"pubmed_authors":["O'Connor Thomas N TN, Zhao Nan N, Orciuoli Haley M HM, Malik Sundeep S, Brasile Alice A, Pietrangelo Laura L, He Miao M, Groom Linda L, Leigh Jennifer J, Mahamed Zahra Z, Liang Chen C, Protasi Feliciano F, Dirksen Robert T RT"],"additional_accession":[]},"is_claimable":false,"name":"Voluntary Wheel Running Mitigates Disease in an Orai1 Gain-of-Function Mouse Model of Tubular Aggregate Myopathy","description":"Tubular aggregate myopathy (TAM) is an inherited skeletal muscle disease associated with progressive muscle weakness, cramps, and myalgia. Tubular aggregates (TAs) are regular arrays of highly ordered and densely packed straight-tubules observed in muscle biopsies; the extensive presence of TAs represent a key histopathological hallmark of this disease in TAM patients. TAM is caused by gain-of-function mutations in proteins that coordinate store-operated Ca2+ entry (SOCE): STIM1 Ca2+ sensor proteins in the sarcoplasmic reticulum (SR) and Ca2+-permeable ORAI1 channels in the surface membrane. Here, we assessed the therapeutic potential of endurance exercise in the form of voluntary wheel running (VWR) in mitigating TAs and muscle weakness in Orai1G100S/+ (GS) mice harboring a gain-of-function mutation in the ORAI1 pore. Six months of VWR exercise significantly increased specific force production, upregulated biosynthetic and protein translation pathways, and normalized both mitochondrial protein expression and morphology in the soleus of GS mice. VWR also restored Ca2+ store content, reduced the incidence of TAs, and normalized pathways involving the formation of supramolecular complexes in fast twitch muscles of GS mice. In summary, sustained voluntary endurance exercise improved multiple skeletal muscle phenotypes observed in the GS mouse model of TAM.","dates":{"publication":"2026-08-04","submission":"2026-08-04"},"accession":"PXD082130","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:112509","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","NEWT:1748418","NCBITaxon:79857","NEWT:1096976","NEWT:3765","NEWT:3767","NEWT:1589","NEWT:1907535","NEWT:135622","NEWT:4615","NEWT:672127","NEWT:35786","NEWT:1580","NEWT:399784","NEWT:96731","NEWT:656064","NEWT:1582","NEWT:3760","NEWT:1584","NEWT:2086595","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:3357","NEWT:111225","NEWT:7719","NEWT:29073","NEWT:5530","NEWT:868565","NEWT:135674","NEWT:1562698","NEWT:79329","NEWT:30069","NEWT:12637","NEWT:59729","NEWT:2164133","NEWT:295105","NEWT:108061","NEWT:60711","NEWT:2020713","NEWT:224308","NEWT:3347","NEWT:49928","NEWT:3349","NEWT:160621","NEWT:2502409","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:37919","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:2714896","NEWT:1424507","NEWT:1194599","NEWT:272844","NEWT:1348799","NEWT:1608994","NEWT:33995","NEWT:55784","NEWT:1303443","NEWT:9483","NEWT:485","NEWT:56636","NEWT:2709072","NEWT:2499525","NEWT:1122981","NEWT:2853422","NEWT:1122984","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:1922344","NEWT:108458","NEWT:5936","NEWT:85692","NEWT:321967","NEWT:320637","NEWT:1078283","NEWT:3750","NEWT:983964","NEWT:11706","NEWT:32644","NEWT:527796","NEWT:279010","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:9054","NEWT:472","NEWT:940825","NEWT:29459","NEWT:529507","NEWT:1071661","NEWT:1380096","NEWT:28128","NEWT:470","NEWT:41122","NEWT:5911","NEWT:1328300","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:166314","NEWT:166313","NEWT:63366","NEWT:63367","NEWT:29488","NEWT:215402","NEWT:1547","NEWT:1290454","NEWT:3726","NEWT:906914","NEWT:81231006","NEWT:30455","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:299467","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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