DOE Data Explorer title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: S. elongatus PCC 7942 Carbon Metabolism Proteomics (MC-DP2) (in EN)

Abstract

The purpose of this experiment was to examine the redox proteome of S. elongatus PCC 7942 CscB/SPS under different light conditions (light and dark) and culture conditions (dense and dilute optical density). Samples were processed using a resin-assisted capture (RAC) workflow with TMT labeling to enrich and quantify protein cysteines which were differentially oxidized under four conditions. The datasets were generated by a Q Exactive Plus Orbitrap Mass Spectrometer coupled with a Waters nanoAcquity UPLC, then searched by MSGF+ for downstream redox PTM analysis.

Publication Date:
Other Number(s):
PNNL-SA-204422
34080
DOE Contract Number:  
AC05-76RL01830
Research Org.:
Pacific Northwest National Laboratory 2; PNNL
Sponsoring Org.:
SC
Collaborations:
Predictive Phenomics Initiative, Pacific Northwest National Laboratory
Subject:
59 BASIC BIOLOGICAL SCIENCES; Predictive Phenomics, S. elongatus PCC 7942, Proteomics, Tandem Mass Tag 16-Plex, global analysis, post translational modifications, central carbon metabolism, circadian rhythm
OSTI Identifier:
2475747
DOI:
https://doi.org/10.25584/PPI/2475747

Citation Formats

S. elongatus PCC 7942 Carbon Metabolism Proteomics (MC-DP2). United States: N. p., 2024. Web. doi:10.25584/PPI/2475747.
S. elongatus PCC 7942 Carbon Metabolism Proteomics (MC-DP2). United States. doi:https://doi.org/10.25584/PPI/2475747
2024. "S. elongatus PCC 7942 Carbon Metabolism Proteomics (MC-DP2)". United States. doi:https://doi.org/10.25584/PPI/2475747. https://www.osti.gov/servlets/purl/2475747. Pub date:Sun Oct 20 20:00:00 EDT 2024
@article{osti_2475747,
title = {S. elongatus PCC 7942 Carbon Metabolism Proteomics (MC-DP2)},
abstractNote = {The purpose of this experiment was to examine the redox proteome of S. elongatus PCC 7942 CscB/SPS under different light conditions (light and dark) and culture conditions (dense and dilute optical density). Samples were processed using a resin-assisted capture (RAC) workflow with TMT labeling to enrich and quantify protein cysteines which were differentially oxidized under four conditions. The datasets were generated by a Q Exactive Plus Orbitrap Mass Spectrometer coupled with a Waters nanoAcquity UPLC, then searched by MSGF+ for downstream redox PTM analysis.},
doi = {10.25584/PPI/2475747},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Sun Oct 20 20:00:00 EDT 2024},
month = {Sun Oct 20 20:00:00 EDT 2024}
}