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}
}
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