Description
To explore the mechanism underlying cardioprotective effects of SM, iTRAQ-based proteomic approach was applied to analyze protein of myocardium in rats with myocardial ischemic injury.
Myocardial tissue of Shenmai-treated mice with left coronary artery ligation were harvest after 7 days treatment. Tissue samples were homogenized with lysis buffer by needle sonication. The solubilized samples were centrifuged at 16,000 � g for 10 min at 4 �C and the total protein in the supernatant was quantified using BCA assay. The relative quantification was calculated based on the ratio of the reporter ions intensities at m/z 117.1, 118.1, 119.1, and 121.1 corresponding to the myocardial ischemia condition as well as treated with RG, OP, and SM, over the reporter ion intensity at m/z 116.1 corresponding to sham-operated condition.
The peak lists were submitted for database sequence searches using ProteinPilot software (version 3.0, Applied Biosystems). The following parameters were set in the searching: trypsin as enzyme, fixed modification of carbamidomethyl labeled cysteine, iTRAQ as sample type, no special factors, biological modification, thorough identification search. Other parameters, such as tryptic cleavage specificity, precursor ion mass accuracy, and fragment ion mass accuracy were built-in functions of ProteinPilot software, and the Paragon method was adopted.
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Shenmai Formula, iTRAQ proteomics
Contact
Principal Investigators:
(in alphabetical order)
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Yi Wang, Zhejiang University, China
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Submitting User: |
zhaoyujoy
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Identification Results |
Proteins (Human, Remapped):
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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.
"N/A" means no results of this type were submitted.
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.
"N/A" means no results of this type were submitted.
Number of distinct peptide sequences (including modified variants or peptidoforms) reported
across all analyses (original submission and reanalyses) associated with this dataset.
"N/A" means no results of this type were submitted.
Total number of peptide-spectrum matches (i.e. spectrum identifications) 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 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.