MassIVE MSV000086774

Partial Public

Site-specific N-linked glycosylation analysis of human carcinoembryonic antigen

Description

CE-MS/MS analysis of a pure carcinoembryonic antigen obtained from patient tissue samples. Enzymes used for digestion: trypsin, Glu-C, pronase. CE separation voltage 20 kV, normal polarity. CE-MS/MS parameters: ESI positive mode, glass capillary voltage at 1200 V, drying gas temperature at 150C, drying gas flow rate at 1.2 L/min, nebulizer gas pressure at 0.2 bar, quadrupole ion energy at 3.0 eV and collision cell energy at 7.0 eV. MS data were acquired between m/z 200 and 2000 with a spectral acquisition rate of 1 Hz. MS/MS spectra were acquired in a data dependent mode with an absolute threshold of 4548 counts and active exclusion. D1 - CEA1 trypsin, D2 - CEA2 trypsin, D3 - CEA3 trypsin, D4 - CEA1 Glu-C, D5 CEA2 Glu-C, D6 - CEA3 Glu-C, D7 - CEA1 pronase, D8 - CEA2 pronase, D9 - CEA3 pronase [doi:10.25345/C5Z50X] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: glycosylation, carcinoembryonic antigen, colorectal cancer, CE-MS

Contact

Principal Investigators:
(in alphabetical order)
Guinevere Lageveen-Kammeijer, LUMC, the Netherlands
Submitting User: VKuzyk
Number of Files:
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Owner Reanalyses
Experimental Design
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Identification Results
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Quantification Results
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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.

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

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

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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.

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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.

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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.