{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/proteinGroups_RawData.txt"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_C3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_D3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_C2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_D1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_D2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_D3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_C3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_C1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_C2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_D2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/B73_D1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065315/EA2024_C1.raw"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["david.caparros@cragenomica.es"],"submitter":["Rocio Arce"],"technology_type":["Mass Spectrometry","Bottom-up proteomics"],"software":[""],"submitter_keywords":["Maize","Drought","B73"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD065315"],"tissue":["Plant Cell","Leaf"],"sample_protocol":["Approximately 1g of leaf tissue from three biological samples of B73 and EA2024 (control and drought) was ground with liquid nitrogen until a fine powder was obtained. Each powdered sample was then mixed with 10 mL of Tris-Mg/NP-40 extraction buffer and vortexed vigorously. RuBisCO protein depletion was performed following the protocol described by Kim et al. (2013) [89]. Finally, samples were stored at −20°C in 80% (v/v) acetone. Samples were sent in cold acetone to the Proteomics Platform of the Parc Científic de Barcelona (Universitat de Barcelona, Spain) for further processing. Briefly, 20 μg of protein from each sample was reduced with DTT, alkylated with IAA, and digested with trypsin in a two-step protocol. The resulting peptides were purified using C18 chromatography and dried for storage at -20°C until analysis.   The dried peptides were resuspended, and 600 ng were injected into a nanoAcquity liquid chromatographer coupled to an LTQ-Orbitrap Velos mass spectrometer (Thermo Scientific, Waltham, USA). Peptides were separated on a C18 reverse-phase column with a gradient elution over 175 minutes. Data-dependent acquisition was performed, with peptide masses (m/z 300–1700) analyzed at a resolution of 60,000. The 15 most abundant peptides per MS scan were then fragmented via Collision-Induced Dissociation. Raw data were processed using Thermo Xcalibur software (v.2.2)."],"repository":["Pride"],"quantification_method":["Not available"],"modification":[""],"data_protocol":["The raw data generated was analyzed with MaxQuant software (v 1.6.3.4) using standardized workflows. The spectra were searched against the UniProt Proteome Zea Mays database (v 190121), including contaminants. For Label-free quantification (LFQ), the minimum ratio count was set to 2, and both razor and unique peptides were used for quantitation. The False discovery rate (FDR) was set to 1% for both protein and Peptide Spectrum Match levels."],"omics_type":["Proteomics"],"labhead":["David Caparros-Ruiz"],"instrument_platform":[""],"labhead_affiliation":["Centre for Research in Agricultural Genomics (CRAG) Consorci CSIC-IRTA-UAB-UB"],"submission_type":["PARTIAL"],"species":["Zea Mays (maize)"],"publication":["10.3389/FPLS.2026.1830066"],"submitter_mail":["rocio.arce@cragenomica.es"],"submitter_affiliation":["Centre for Research in Agricultural Genomics (CRAG) Consorci CSIC-IRTA-UAB-UB"],"submitter_country":["Spain"],"additional_accession":[]},"is_claimable":false,"name":"Proteomics analysis of B73 and EA2024 maize plants under control and drought conditions","description":"The maize plants were grown in culture chambers (16/8 hours day/night, 25/22ºC, 50% humidity) until 15 days, when the third leaf was fully developed. Then, for drought treatment, irrigation was completely stopped for 10 days when the samples were collected, in parallel to control plants that were irrigated for the same 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