Dataset Information

ACD - Relative quantitative proteomic analysis reveals wound response proteins correlated with after-cooking darkening

ABSTRACT: Proteomic analysis of After-cooking darkening

INSTRUMENT(S): Qtrap

ORGANISM(S): Solanum Tuberosum (potato)

SUBMITTER: Patrick Murphy

LAB HEAD: Patrick Murphy

PROVIDER: PRD000233 | Pride | 2012-03-04

REPOSITORIES: Pride

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Dataset's files

Source:

			Action	DRS
	PRIDE_Exp_Complete_Ac_12225.pride.mgf.gz	Mgf
	PRIDE_Exp_Complete_Ac_12225.pride.mztab.gz	Mztab
	PRIDE_Exp_Complete_Ac_12225.xml.gz	Xml
	PRIDE_Exp_Complete_Ac_12226.pride.mgf.gz	Mgf
	PRIDE_Exp_Complete_Ac_12226.pride.mztab.gz	Mztab

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Publications

Relative quantitative proteomic analysis reveals wound response proteins correlated with after-cooking darkening.

Murphy J Patrick JP Kong Fanming F Pinto Devanand M DM Wang-Pruski Gefu G

Proteomics 20101201 23

Many common potato tuber defects are difficult to elucidate because of the degree of genetic complexity involved, making systems biology approaches necessary. Interaction between chlorogenic acid and iron is responsible for the darkening of potato tuber tissues upon heating--termed after-cooking darkening (ACD). To explore mechanisms of darkening severity in tuber tissues, we have employed relative quantitative proteomics to discover differentially expressed proteins involved in ACD. Tuber tissu ...[more]

PMID: 21058337

Similar Datasets

Project description:Application of a novel TiO2-based phosphopeptide enrichment protocol to study the role of protein arginine phosphorylation in B.subtilis. 1 iTRAQ Quantification of pArg peptides in B.subtilis upon heat shock and oxidative stress in comparison to unstressed control 2 Studying pArg upon deletion of McsB protein arginine kinase in B.subtilis (double mutant cells for McsB and YwlE phosphoarginine phosphatase) 3 Studying pArg in wt cells upon inhibition of YwlE phosphatase with cell wall permeable inihbitor sodium pervanadate Short overview McsB is a bacterial protein arginine kinase that is involve in stress adaptation for heat shock and oxidative stress - cells were grown in LB medium until O.D. 0.6 and split into 3 fractions - one fraction was treated with heat stress for 20 min at 50 degrees C, one was stressed with 1mM diamide (induced oxidative foldeing stress), and one was kept at 37 degrees C (control) - cell harvest, lysis with a modified FASP protocol including tryptic cleavage - iTRAQ labelling for some experiments - TiO2 enrichment to purify all phosphopeptides - LC-MS/MS analysis of phosphopetides - phosphosite localization by phosphoRS and manually - quantitation of phosphorylation relative to protein abundance in the different samples. Peptide and protein identification: Raw data were extracted by the Protein Discoverer software suite (version 1.2.227 for wt phosphorylation, all 4 replicates of the iTRAQ/TiO2 pArg study and replicates 1 and 2 for the pervanadate and the double mutant experiments and version 1.3.0.339 for protein abundance determination, and replicates 3 and 4 of the pervanadate and double mutant experiments. Thermo-Fisher Scientific) and searched against a combined forward/reversed database of B. subtilis protein sequences and common contaminants using MASCOT (version 2.2, www.matrixscience.com). Since cells were grown in LB medium, all raw data were independently searched against a combined B. subtilis and yeast (S. cerevisae) database which did not result in a significant increase in protein hits or identification of yeast proteins. Carbamidomethylation of cysteine, iTRAQ modification of peptide Nterminus and lysine;-amino group were set as fixed modifications. Phosphorylation of serine, threonine, tyrosine, histidine, and arginine as well as methionine sulfoxidation were selected to be variable, with a maximum of 4 modifications per peptide. Since tryptic cleavage is impaired at phosphorylated arginine, a maximum of two missed cleavage sites was allowed, whereas fully tryptic cleavage of both termini was required. The peptide mass deviation was set to 4 ppm; fragment ions were allowed to have a mass deviation of 0.5 Da for CID and ETD data and 0.025 Da for HCD data. False discovery rates were assessed from reversed database hits including all identified peptide spectrum matches with MASCOT score above 19, rank 1, and a peptide length of at least 6 amino acids. This resulted in false discovery rates below 1 % on the peptide spectrum match level and below 1.5% on the unique peptide level for each experiment. For reliable phosphorylation site analysis, all phosphopeptide hits were automatically re-analyzed by the phosphoRS software (Taus et al, 2011) within the Protein Discoverer software suite, manually validated, and compared to known B. subtilis protein phosphorylations (Macek et al, 2007). Proteins were grouped according to their biological function assignment on the SubtiList homepage (http://genolist.pasteur.fr/SubtiList/). Relative quantification of phosphorylation: Peptide quantification was achieved by the reporter ions quantifier node in Protein Discoverer. This node extracted reporter ion areas from corresponding HCD scans for all identified peptide hits (HCD, CID and ETD) based on the precursor mass. Extracted peak areas for heat shock and oxidative stress were divided by the peak area of the control sample to give the corresponding peptide abundance ratio. Regulatory cut-offs for peptide abundance ratios were determined from the distribution of unphosphorylated peptides. A 95% confidence window was applied to log2 normalized values of peptide regulations and all hits outside of this window were considered to be regulated. For the heat stress/control ratio regulatory cut-off values of 0.59 and 1.75 were determined. Peptides with abundance changes within 0.30 to 2.50 for the oxidative stress/control ratio were not considered to be regulated. Protein regulations were the averages of all identified and quantified unphosphorylated peptides from all analyzed samples (Supplementary Table 5). Phosphopeptide abundances were calculated by averaging, if a phosphopeptide was identified in several replicates and/or charge states. To argument for upregulation of phosphorylation, each phospho-peptide ratio was divided by the respective protein abundance ratio, in case the protein was identified before. For regulation of the phosphorylation, we oriented the regulatory cut-offs determined before. We compared each phosphopeptide abundance against the respective protein abundance and determined a twofold regulation to be significant.