Abstract
Protein turnover is vital for cellular functioning and is often associated with the pathophysiology of a variety of diseases. Metabolic labeling with heavy water followed by liquid chromatography coupled to mass spectrometry is a powerful tool to study in vivo protein turnover in high throughput and large scale. Heavy water is a cost-effective and easy to use labeling agent. It labels all nonessential amino acids. Due to its toxicity in high concentrations (20% or higher), small enrichments (8% or smaller) of heavy water are used with most organisms. The low concentration results in incomplete labeling of peptides/proteins. Therefore, the data processing is more challenging and requires accurate quantification of labeled and unlabeled forms of a peptide from overlapping mass isotopomer distributions. The work describes the bioinformatics aspects of the analysis of heavy water labeled mass spectral data, available software tools and current challenges and opportunities.
| Original language | English (US) |
|---|---|
| Article number | bbab598 |
| Journal | Briefings in Bioinformatics |
| Volume | 23 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 1 2022 |
Keywords
- evolution of deuterium-enriched mass isotopomers
- nonlinear models of time course data
- protein turnover
- rate constant estimation from metabolic labeling with heavy water followed by liquid chromatography - mass spectrometry (LC-MS)
ASJC Scopus subject areas
- Information Systems
- Molecular Biology