MassIVE MSV000088001

Partial Public

Lung cancer plasma glycoproteome correlation with plasma DSC thermograms

Description

Blood plasma from patients diagnosed with different subtypes of lung cancer or subjects with benign nodules was analyzed by using isobaric labeling and correlating to plasma thermograms. Plasma samples were digested using a FASP approach, labeled with TMT11plex reagents, admixed, deglycosylated using NEB Deglycoslylation Mix II in a non-denaturing approach. Deglycosylated peptides were eluted and analyzed by 1DLC-(low pH RP C-18)-MS. Collected data were analyzed by PD 2.1 using SequestHT and Mascot considering N-linked de-glycosylation of plasma proteins with Asn>Asp and Gln>Glu conversions along with standard modifications (TMT, Met(ox), Cys(CAM)) using an Orbitrap ELITE mass spectrometer. TMT reporter ion values were normalized to pooled internal standard TMT131 label and median glycopeptide abundance values of selected proteins were compared between control subjects and LC patients. [doi:10.25345/C5PG3P] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: lung cancer ; differential scanning calorimetry ; glycoproteomics

Contact

Principal Investigators:
(in alphabetical order)
Michael L. Merchant, PhD, University of Louisville, USA
Submitting User: mmerchant
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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 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 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.
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