{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/checksum.txt"],"Pdf":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/analytical_Service_Report_for_TMT_based_Quantitative_Proteomic_Analysis.pdf"],"Csv":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/database_searching_result_proteinGroups.csv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/database_searching_result_peptides.csv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Experimental_Design.csv"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_5.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_6.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/06/PXD079929/TMT_Fraction_2.raw"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"labhead_mail":["KIARISH@cop.sc.edu"],"submitter":["Kim-Tuyen Huynh-Dam"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Circulating liquidome","Tmt-10plex","Peromyscus","Gene canalization","Serum","Bond disruption","Social stress","Deer mouse","Pair-bonding"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD079929"],"tissue":["Blood Serum"],"sample_protocol":["Serum was extracted from Bonded (B) and Bond-Disrupted (BD) deer mice. Proteins were extracted, reduced, alkylated, and subjected to in-solution trypsin digestion. The resulting peptides were labeled using a TMT-10plex isobaric mass tagging kit. The labeled samples were pooled multiplexed into a single tube, desalted, and fractionated into 6 fractions prior to LC-MS/MS analysis on a Thermo Q Exactive mass spectrometer."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["The 6 raw MS fractions were analyzed using MaxQuant (version 1.6.2.14) and searched against the Peromyscus protein database. Carbamidomethylation of cysteine was set as a fixed modification, while oxidation of methionine was set as a variable modification. TMT-10plex reporter ion quantification was enabled. Enzyme specificity was set to trypsin with a maximum of 2 missed cleavages. Precursor ion mass tolerance was set to 10 ppm, and MS/MS fragment tolerance was 0.6 Da."],"omics_type":["Proteomics"],"labhead":["Hippokratis Kiaris"],"instrument_platform":[""],"labhead_affiliation":["The Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina"],"submission_type":["PARTIAL"],"species":["Peromyscus"],"submitter_mail":["kimtuyenhuynhdam@gmail.com"],"publication":["38114920 Naderi A, Liles K, Burns T, Chavez B, Huynh-Dam KT, Kiaris H. Pair bonding and disruption impact lung transcriptome in monogamous Peromyscus californicus. BMC Genomics. 2023 24(1):789 10.1186/s12864-023-09873-6"],"submitter_affiliation":["University of South Carolina"],"submitter_country":["United States"],"pubmed_abstract":["Social interactions affect physiological and pathological processes, yet their direct impact in peripheral tissues remains elusive. Recently we showed that disruption of pair bonds in monogamous Peromyscus californicus promotes lung tumorigenesis, pointing to a direct effect of bonding status in the periphery (Naderi et al., 2021). Here we show that lung transcriptomes of tumor-free Peromyscus are altered in a manner that depends on pair bonding and superseding the impact of genetic relevance between siblings. Pathways affected involve response to hypoxia and heart development. These effects are consistent with the profile of the serum proteome of bonded and bond-disrupted Peromyscus and were extended to lung cancer cells cultured in vitro, with sera from animals that differ in bonding experiences. In this setting, the species' origin of serum (deer mouse vs FBS) is the most potent discriminator of RNA expression profiles, followed by bonding status. By analyzing the transcriptomes of lung cancer cells exposed to deer mouse sera, an expression signature was developed that discriminates cells according to the history of social interactions and possesses prognostic significance when applied to primary human lung cancers. The results suggest that present and past social experiences modulate the expression profile of peripheral tissues such as the lungs, in a manner that impacts physiological processes and may affect disease outcomes. Furthermore, they show that besides the direct effects of the hormones that regulate bonding behavior, physiological changes influencing oxygen metabolism may contribute to the adverse effects of bond disruption."],"pubmed_title":["Pair bonding and disruption impact lung transcriptome in monogamous Peromyscus californicus."],"pubmed_authors":["Naderi A A, Liles K K, Burns T T, Chavez B B, Huynh-Dam K-T KT, Kiaris H H"],"additional_accession":[]},"is_claimable":false,"name":"Quantitative serum proteomics of monogamous deer mice (Peromyscus) reveals systemic alterations driven by pair-bonding and bond disruption","description":"This dataset contains TMT-10plex quantitative proteomics of serum isolated from monogamous deer mice (Peromyscus). The study investigates the systemic physiological impact of social interactions, specifically comparing pair-bonded animals to those that have experienced bond disruption. The circulating serum proteome was analyzed to identify factors that mediate peripheral tissue responses to social history. This serum data supports findings regarding the impact of social bonds on the lung transcriptome (Naderi et al., 2023, BMC Genomics) and systemic transcriptomic stochasticity/gene canalization in cultured 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