{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Tabular":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/report.pg_matrix.tsv","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/report.pr_matrix.tsv"],"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/checksum.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Match_result_README.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090128-1A.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090129-1A.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090127-1A.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090125-1A.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090126-1A.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/Astral-1_24_FPEP240090124-1A.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065386/2495815_protein_genomic.fasta"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["1176044269@qq.com"],"submitter":["lvqin he"],"technology_type":["Mass Spectrometry","Data-independent acquisition"],"software":[""],"submitter_keywords":["Glaesserella parasuis；qseb"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD065386"],"tissue":["Cell Culture"],"sample_protocol":["Select the parent strain SC1401 and the Δ qseB gene deficient strain of Haemophilus parasuis separately and transfer them to 3 ml of TSA++medium. Place them in a 37 ℃ air shaker and perform enrichment culture at 220 rpm. Then streak and inoculate them onto TSA++medium. Incubate overnight at 37 ℃, and the next day pick a single colony and inoculate it in TSB++medium. Cultivate at 37 ℃ and 220 rpm until OD600nm reaches 1.6, collect bacterial sediment by centrifugation and store at -80 ° C for future use. Take out tissue samples from a -80 ℃ refrigerator, grind them into powder at low temperature, quickly transfer them to a liquid nitrogen pre cooled centrifuge tube, add an appropriate amount of SDT (containing 100mM NaCl) and dissolve with 1/100 volume of dithiothreitol (DTT), shake and mix well, and sonicate in an ice water bath for 5 minutes to fully lyse. React at 95 ℃ for 8-15 minutes, ice bath for 2 minutes, centrifuge at 4 ℃ and 12000 g for 15 minutes, add sufficient iodoacetamide (IAM) solution to the supernatant, and let it react in the dark for 1 hour. Add 4 times the volume of -20 ℃ pre cooled acetone and precipitate at -20 ℃ for at least 2 hours. Centrifuge at 4 ℃ and 12000 g for 15 minutes, and collect the precipitate. Afterwards, add 1 mL of pre cooled acetone at -20 ℃ and resuspend, wash the precipitate, collect the precipitate, air dry it, and the precipitate is the total protein. Add an appropriate amount of Dissolved Buffer (DB buffer) to thoroughly dissolve the protein precipitate."],"repository":["Pride"],"modification":[""],"quantification_method":[""],"data_protocol":["Search and analyze raw files using the DIA-NN search software based on the uniprot protein database. In order to improve the quality of analysis results, DIA-NN software further filters the retrieval results: Peptide Spectrum Matches (PSMs) with a credibility of over 99% are considered trustworthy PSMs, only trustworthy peptides and proteins are retained, and FDR validation is performed to remove peptides and proteins with FDR greater than 1%. Perform GO and IPR functional annotation using interprescan software, and perform functional protein family and pathway analysis on identified proteins using COG and KEGG. Conduct volcano map analysis, cluster heatmap analysis, and pathway enrichment analysis for GO, IPR, and KEGG for DEP, and use STRINGDB software to predict possible protein-protein interactions."],"omics_type":["Proteomics"],"labhead":["Experimental animal center"],"instrument_platform":[""],"labhead_affiliation":["Southwest Medical University"],"submission_type":["PARTIAL"],"species":["Glaesserella Parasuis Sh0165"],"submitter_mail":["1176044269@qq.com"],"publication":["Not available"],"submitter_affiliation":["southwest medical university"],"submitter_country":["China"],"additional_accession":[]},"is_claimable":false,"name":"DIA quantitative proteomics-QseB","description":"We perform proteomic analysis on the parent strain SC1401 and the ΔqseB gene deletion mutant under standard growth conditions. The proteomic data will provide useful insights for the whole-system modeling of signal transduction and gene transcription regulation. This serves as an important foundation for further research into the role of QseB during Glaesserella parasuis infection, the pathogenic mechanisms of Glaesserella parasuis, as well as its prevention and 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