MassIVE MSV000087049

Partial Public

Truncation of the N-terminus of cardiac troponin I initiates adaptive remodeling of the myocardial proteosome via phosphorylation of mechano-sensitive signaling pathways

Description

We employed isobaric labeled peptides to do bottom-up proteomics to quantify both non-enriched total peptides and enriched phospho-peptides obtained from hearts of control mice expressing wild-type cardiac troponin I and transgenic mice expressing the truncated N-terminal cardiac troponin I. [doi:10.25345/C5Q80S] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Sarcomeres ; Paxillin ; Cytoskeleton ; Integrin ; Heart ; Mouse

Contact

Principal Investigators:
(in alphabetical order)
R. John Solaro, University of Illinois-Chicago, USA
Submitting User: cmwarren_8
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Experimental Design
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Identification Results
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Quantification Results
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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 proteins found to be differentially abundant in at least one comparison across all analyses (original submission and reanalyses) associated with this dataset.

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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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