Large-scale phosphorylation analysis of mouse liver
By J. Villén, S. Beausoleil, S. Gerber, Steven P. Gygi. 2007
735 citations recorded by the source corpus.
Subfields: Materials Chemistry, Molecular Biology, Spectroscopy
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Materials Chemistry
- Matthias Mann
- J. Villén
- Steven P. Gygi
- Francesca Diella
- Juri Rappsilber
- Toby J. Gibson
- Zsuzsanna Dosztányi
In Molecular Biology
- Matthias Mann
- John R. Yates III
- R. Shaw
- C. Ruse
- A. Nakorchevsky
- Juri Rappsilber
- Jesper V. Olsen
- Steven P. Gygi
In Spectroscopy
- Matthias Mann
- Jesper V. Olsen
- John R. Yates III
- C. Ruse
- A. Nakorchevsky
- Juri Rappsilber
- Steven P. Gygi
- Jüergen Cox
Citations in the corpus
- Mammalian Ceramide Synthases (2010, background): “Data from high performance mass spectrometry support a suggestion that mouse liver CerS2 and CerS5 might be phosphorylated (33).”
- AMPK phosphorylation of raptor mediates a metabolic checkpoint. (2008, background): “Notably, during the course of this study, two large-scale analyses of phosphoproteins from rat and mouse liver revealed phosphorylation of endogenous raptor at Ser722, suggesting that it is indeed a bona fide phosphorylation site in vivo (Moser and White, 2006; Villen et al., 2007).”
- A tissue-specific atlas of mouse protein phosphorylation and expression. (2010, neutral): “Distribution of Phosphorylation Site Classes across Tissues and Phosphoproteins Phosphorylation sites were classified as acidic, basic, proline-directed, tyrosine, or other as described (Villen et al., 2007).”
- Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle. (2008, methodology): “The remaining part was directly digested prior to fractionation of the resulting peptides by strong cation exchange (SCX) chromatography (Beausoleil et al., 2004; Olsen et al., 2006; Villen et al., 2007).”
- Decision Tree-Driven Tandem Mass Spectrometry for Shotgun Proteomics (2008, methodology): “Results Characterization of peptide identification probabilities To gather a training set of MS/MS spectra for probability calculations, we digested two aliquots of a whole-cell yeast lysate (that is, two biological replicates) using the protease endo-LysC and separated each into 12 fractio”
- Phospho.ELM: a database of phosphorylation sites—update 2008 (2007, background): “For this reason, we consider it increasingly important to create and maintain publicly available phospho-protein databases, where the exponentially increasing number of known phosphorylation sites (7–12) can be easily accessed by the research community.”
- Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips (2007, methodology): “Enrichment of phosphopeptides in HeLa cytoplasmic extracts There have been only a few reports of the application of phosphopeptide enrichment methods to real, complex samples such as crude cell extracts including very recent large-scale studie”
- The SCX/IMAC enrichment approach for global phosphorylation analysis by mass spectrometry (2008, methodology): “However, the method that has proven most comprehensive in mapping the phosphoproteome is SCX chromatography combined with either IMA”
- Proteomics by mass spectrometry: approaches, advances, and applications. (2009, methodology): “Proteome-scale screening of phosphotyrosines has been extended to the identification of oncogenic kinases (209), identification of core proteins responding to drug treatment (210), and definition of the organspecific phosphorylation (201).”