MassIVE MSV000079563

Imported Reanalysis Dataset Public PXD000208

AP-MS analysis of human histone deacetylase interactions in CEM-T cells

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Description

Affinity purification-mass spectrometry (AP-MS) datasets of eleven human histone deacetylases (HDACs). Affinity-tagged (GFP) HDACs were expressed in a human CEM-T cell line. For label-free analysis, proteins were digested by trypsin in-solution and peptides separated across a linear 180 min gradient by a one-dimensional LC-MS/MS analysis. For label-free analysis, MS data (RAW files) were converted into mzXML format using the Proteowizard conversion tool. mzXML files were searched using the X!Tandem/k-score database search tool against the human subset of the UniProt protein sequence database, appended with a list of common sample contaminants. The search results were processed using PeptideProphet and ProteinProphet tools. The data from individual experiments across 7 biological replicates of GFP controls and 23 HDAC-GFP-tagged biological replicates were merged, and the spectral counts were extracted using the software, ABACUS. The combined list of protein identifications (protein groups) was filtered to achieve a protein-level FDR of less than 1%. When computing the spectral counts in individual experiments, proteins were quantified (i.e. spectra counted) if they were identified with a probability equal or greater than 0.9 in that particular replicate. For metabolic labeling IDIRT experiments, isolated proteins were separated by SDS-PAGE, digested by trypsin in-gel, and peptides were separated across a linear 90 min gradient. RAW files were processed and peptides were identified (less than 1% FDR) and quantified using SEQUEST/Percolator in the Proteome Discoverer software (v1.3). IDIRT protein ratios were normalized by the median SILAC protein ratio determined from 1D-LC-MS/MS analysis of input lysates. Protein interactions have been submitted to the IMEx consortium through IntAct with the identifier IM-18733. [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: HDAC ; AP-MS ; protein interactions ; IDIRT

Contact

Principal Investigators:
(in alphabetical order) 		None Listed
Submitting User: ccms

Publications

Joshi P, Greco TM, Guise AJ, Luo Y, Yu F, Nesvizhskii AI, Cristea IM.
The functional interactome landscape of the human histone deacetylase family.
Mol. Syst. Biol.

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Number of distinct conditions across all analyses (original submission and reanalyses) associated with this dataset.

Distinct condition labels are counted across all files submitted in the "Metadata" category having a "Condition" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct biological replicates across all analyses (original submission and reanalyses) associated with this dataset.

Distinct replicate labels are counted across all files submitted in the "Metadata" category having a "BioReplicate" or "Replicate" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct technical replicates across all analyses (original submission and reanalyses) associated with this dataset.

The technical replicate count is defined as the maximum number of times any one distinct combination of condition and biological replicate was analyzed across all files submitted in the "Metadata" category. In the case of fractionated experiments, only the first fraction is considered.

"N/A" means no results of this type were submitted.
Originally identified proteins that were automatically remapped by MassIVE to proteins in the SwissProt human reference database.

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Number of distinct protein accessions reported across all analyses (original submission and reanalyses) associated with this dataset.

"N/A" means no results of this type were submitted.
Number of distinct unmodified peptide sequences reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct peptide sequences (including modified variants or peptidoforms) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Total number of peptide-spectrum matches (i.e. spectrum identifications) reported across all analyses (original submission and reanalyses) associated with this dataset.

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Number of distinct proteins quantified across all analyses (original submission and reanalyses) associated with this dataset.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
Number of distinct proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

A protein is differentially abundant if its change in abundance across conditions is found to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated with statistical tests for differential abundance.

Distinct protein accessions are counted across all files submitted in the "Statistical Analysis of Quantified Analytes" category having a "Protein" column in this dataset.

"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE. It has been imported to MassIVE for reanalysis purposes, so its spectra data here may consist solely of processed peak lists suitable for reanalysis with most software.