Cargando…
High-Resolution Mass Spectrometry for In Vivo Proteome Dynamics using Heavy Water Metabolic Labeling
Cellular proteins are continuously degraded and synthesized. The turnover of proteins is essential to many cellular functions. Combined with metabolic labeling using stable isotopes, LC–MS estimates proteome dynamics in high-throughput and on a large scale. Modern mass spectrometers allow a range of...
Autor principal: | Sadygov, Rovshan G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672638/ https://www.ncbi.nlm.nih.gov/pubmed/33105654 http://dx.doi.org/10.3390/ijms21217821 |
Ejemplares similares
-
Quantifying label enrichment from two mass isotopomers increases proteome coverage for in vivo protein turnover using heavy water metabolic labeling
por: Deberneh, Henock M., et al.
Publicado: (2023) -
Software Tool for Visualization and Validation of Protein Turnover Rates Using Heavy Water Metabolic Labeling and LC-MS
por: Deberneh, Henock M., et al.
Publicado: (2022) -
High Mass Accuracy Phosphopeptide Identification Using Tandem Mass Spectra
por: Sadygov, Rovshan G.
Publicado: (2012) -
A large-scale LC-MS dataset of murine liver proteome from time course of heavy water metabolic labeling
por: Deberneh, Henock M., et al.
Publicado: (2023) -
Altered Retinoic Acid Metabolism in Diabetic Mouse Kidney Identified by (18)O Isotopic Labeling and 2D Mass Spectrometry
por: Starkey, Jonathan M., et al.
Publicado: (2010)