{"database":"Pride","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/proteinGroups.txt","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/checksum.txt"],"Xml":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/mqpar.xml"],"Raw":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/T4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/C3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/T2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/C1.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/C4.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/C2.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/T3.raw","ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/T1.raw"],"Fasta":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/uniprotkb_proteome_UP000215914_2024_12_12.fasta"],"Mztab":["ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2026/05/PXD065296/mzTab.mzTab"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"labhead_mail":["pl.alves@unesp.br"],"submitter":["Felipe Silva"],"technology_type":["Data-dependent acquisition","Mass Spectrometry"],"software":[""],"submitter_keywords":["stressed plants","Allelophaty; bidens sulphurea; panicum maximum; bioherbicides; stressed plants","bioherbicides","bidens sulphurea","panicum maximum","Allelophaty"],"full_dataset_link":["https://www.ebi.ac.uk/pride/archive/projects/PXD065296"],"tissue":["Plant Cell","Leaf"],"sample_protocol":["Samples containing 1 g of pulverized plant material macerated in liquid nitrogen were transferred to fresh tubes, and 3 mL of extraction buffer (500 mM Tris, pH 8.0, 50 mM EDTA, 100 mM KCl, and 1% b-mercaptoethanol) were added. After 5 minutes of shaking on ice, an equal volume of equilibrated phenol solution (Sigma-Aldrich) was added to the extract and homogenized for 5 min at room temperature. After 10 min of centrifugation at 4100g, the organic and aqueous phases were separated. Proteins were precipitated from the phenol phase by the addition of 4 times the volume of cold precipitating solution (0.1 M ammonium acetate in methanol) for 16h at –20° C followed by centrifugation at 4100g for 20 min at 4° C. Subsequently, the protein pellets were washed twice in 1 mL of ice-cold acetone, followed by centrifugation at 4100g for 5 min. The proteins were resuspended in 100 uL of sample buffer (HEPES 50mM). Protein extract concentration was determined by the method described by Bradford (1976) using bovine serum albumin concentrations (0.0625, 0.125, 0.25, 0.5 mg L¯¹) for the standard curve. A total of 100 ug of proteins per sample was precipitated in 0.1 M ammonium acetate in methanol (40 minutes at 4° C). The protein pellet was obtained by centrifugation at 4,000 g (5 min) and resuspended in 1 mL of 25 mM ammonium bicarbonate (AmBic). After 10 minutes of incubation at 70° C, a reducing solution (30 mg DTT in 1 ml of 25 mM AmBic) was added, and the mixture was kept at 56°C for 20 min. Subsequently, the sample was cooled, and 60 uL of alkylation solution (36 mg of IAA in 1 mL of 25 mM AmBic) was added to the mixture. The solution was kept in the dark for 20 minutes. Finally, the digestion solution containing trypsin was added in a ratio of 1:10 (enzyme:protein) and incubated for 12 hours. The peptide extract was dried by vacuum centrifugation and resuspended in water with 0.1% FA (formic acid). Then, the samples were desalted using Millipore Ziptip C18 columns (Sigma-Aldrich) as recommended by the manufacturer and resuspended in 0.1% FA. The peptides were injected into the mass spectrometer after separation by reverse-phase chromatography using an EASY-nLC 1000 system. After loading onto the analytical column, the tryptic peptides were separated on a nano-C18 column (15 cm, 2 μm, 100 Å) over 120 minutes, with a flow rate of 300 nL/min. The instrument used for mass spectrometry analyses was the Q-Exactive (Thermo Scientific), which used a data-dependent acquisition method for the ten most abundant ions. Fragmentation spectra acquisition occurred after high-energy collision dissociation (HCD) fragmentation of the isolated peptide ions."],"repository":["Pride"],"quantification_method":[""],"modification":[""],"data_protocol":["The identification of tryptic peptides and protein inference from C. sulphureus was performed using MaxQuant software [v.2.6.6.0] by correlating experimental data with the protein database of Helianthus annuus available on the UniProtKB platform. The search parameters were set as 20 ppm for precursor ions, oxidation of methionines as a variable modification, and carbamidomethylation of cysteines as a static modification, with a maximum of two missed cleavages and FDR 1%. Label Free Quantification (LFQ) was used for the relative quantification of identified proteins. A total of 8 samples were used, from which four replicates of the control and 4 of the drought stress study. Proteins were only considered if present in at least one biological replicate under these conditions. Abundance values (LFQ) were normalized for each protein/sample in relation to their spectral count. Data were imported into the Perseus software, and for each sample, values were log2 transformed and missing values imputed using a normal distribution that the software had developed. The control and treatment groups were compared using the Student's t-test (p<0.05) for each protein individually, and a fold change of 2 times was used to search for differentially abundant proteins. Hence, functional annotation of all identified proteins in the control and treatment group was performed using EGGNog-mapper v2."],"omics_type":["Proteomics"],"labhead":["Pedro Luis"],"instrument_platform":[""],"labhead_affiliation":["São Paulo State University (Unesp), School of Agricultural and Veterinarian Sciences, Department of Biology, Jaboticabal, Brazil"],"submission_type":["COMPLETE"],"species":["Cosmos Sulphureus"],"submitter_mail":["far.silva@unesp.br"],"publication":["Not available"],"submitter_affiliation":["University of São Paulo"],"submitter_country":["Brazil"],"doi":["10.6019/PXD065296"],"additional_accession":[]},"is_claimable":false,"name":"Impact of drought stress at 40% of field capacity on the allelopathic potential of Cosmos sulphureus Cav under greenhouse experiment","description":"Allelopathic management involves the use of natural compounds produced by plants to suppress weed growth, offering an eco-friendly alternative to synthetic herbicides. Cosmos sulphureus has shown allelopathic potential, but one of the challenges is the typically low concentration of allelochemicals. Environmental stress, such as drought, may stimulate the production of these compounds. This study evaluated the effect of drought stress at 40% field capacity, for fifteen days, at the initial reproductive stage, on the increase of the allelopathic potential of C. sulphureus. The plants were subjected to drought stress. After this period, fresh leaves were collected for malondialdehyde and proteomic tests; and used to prepare a crude extract. Bioassays were performed on Lactuca sativa, Sorghum bicolor, Urochloa decumbens, Cucumis sativus, and Panicum maximum. All extracts significantly inhibited germination (5–90%), depending on the species, concentration, and treatment. Extracts from stressed plants showed lower bioactivity on germination (22,74%), shoot (43,91%) and root growth (35,60%) compared to non-stressed extracts (15,69, 44,70, 33,65% respectively)  with no significant differences occurring between the treatment conditions. It is concluded that drought stress at 40% field capacity, for fifteen days, at the initial reproductive stage, in Cosmos sulphureus plants, does not induce an increase in the allelopathic potential of this species. These findings open avenues for further research into its bioherbicidal activity and the exploration of novel herbicidal mechanisms of action, contributing to the de-velopment of sustainable weed management 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