Metabolic stable isotope labeling followed by liquid chromatography coupled with mass spectrometry (LC-MS) is a powerful tool for in vivo protein turnover studies of individual proteins on a large scale and with high throughput. Turnover rates of thousands of proteins from dozens of time course experiments are determined by data processing tools, which are essential components of the workflows for automated extraction of turnover rates. The development of sophisticated algorithms for estimating protein turnover has been emphasized. However, the visualization and annotation of the time series data are no less important. The visualization tools help to validate the quality of the model fits, their goodness-of-fit characteristics, mass spectra...
Abstract Background Data generated from liquid chromatography coupled to high-resolution mass spectr...
High-throughput multiplexed protein quantification using mass spectrometry is steadily increasing in...
Protein turnover represents an important mechanism in the functioning of cells, with deregulated syn...
Trötschel C, Albaum S, Wolff D, et al. Protein turnover quantification in a multi-labeling approach ...
Metabolic labeling with heavy water followed by LC–MS is a high throughput approach to study proteos...
Protein turnover is a well-controlled process in which polypeptides are constantly being degraded an...
Protein turnover is a well-controlled process in which polypeptides are constantly being degraded an...
<div><p>Protein turnover is a well-controlled process in which polypeptides are constantly being deg...
Proteins are continually produced and degraded, to avoid the accumulation of old or damaged molecule...
Rate constant estimation with heavy water requires a long-term experiment with data collection at mu...
Classical quantitative proteomics studies focus on the relative or absolute concentration of protein...
ABSTRACT: Selected reaction monitoring (SRM) is a mass spectrometry method with documented ability t...
The synthesis of new proteins and the degradation of old proteins in vivo can be quantified in seria...
Selected reaction monitoring (SRM) is a mass spectrometry method with documented ability to quantify...
Targeted proteomics allows researchers to study proteins of interest without being drowned in data f...
Abstract Background Data generated from liquid chromatography coupled to high-resolution mass spectr...
High-throughput multiplexed protein quantification using mass spectrometry is steadily increasing in...
Protein turnover represents an important mechanism in the functioning of cells, with deregulated syn...
Trötschel C, Albaum S, Wolff D, et al. Protein turnover quantification in a multi-labeling approach ...
Metabolic labeling with heavy water followed by LC–MS is a high throughput approach to study proteos...
Protein turnover is a well-controlled process in which polypeptides are constantly being degraded an...
Protein turnover is a well-controlled process in which polypeptides are constantly being degraded an...
<div><p>Protein turnover is a well-controlled process in which polypeptides are constantly being deg...
Proteins are continually produced and degraded, to avoid the accumulation of old or damaged molecule...
Rate constant estimation with heavy water requires a long-term experiment with data collection at mu...
Classical quantitative proteomics studies focus on the relative or absolute concentration of protein...
ABSTRACT: Selected reaction monitoring (SRM) is a mass spectrometry method with documented ability t...
The synthesis of new proteins and the degradation of old proteins in vivo can be quantified in seria...
Selected reaction monitoring (SRM) is a mass spectrometry method with documented ability to quantify...
Targeted proteomics allows researchers to study proteins of interest without being drowned in data f...
Abstract Background Data generated from liquid chromatography coupled to high-resolution mass spectr...
High-throughput multiplexed protein quantification using mass spectrometry is steadily increasing in...
Protein turnover represents an important mechanism in the functioning of cells, with deregulated syn...