Stable isotope labeling by amino acids in cell culture (SILAC) enables the relative quantification of protein amounts and posttranslational modifications in complex biological samples through the use of stable heavy isotope-labeled amino acids. Here we describe methods for the application of SILAC to fission yeast Schizosaccharomyces pombe using either labeled lysine or a combination of labeled lysine and labeled arginine. The latter approach is more complicated than the use of labeled lysine alone but may yield a more comprehensive (phospho)proteomic analysis. The protocol includes methods for construction of SILAC-compatible strains, growth of cultures in labeled medium, cell harvesting, and protein extraction
We describe a synthesis strategy for the preparation of lysine isotopologues that differ in mass by ...
Metabolic labeling with stable isotopes is a prominent technique for comparative quantitative proteo...
We describe a protocol for multiplexed proteomic analysis using neutron-encoded (NeuCode) stable iso...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
Since its introduction in 2002 'stable isotope labeling by amino acids in cell culture' (SILAC) has ...
Modern mass spectrometry (MS)-based approaches are capable of identifying and quantifying thousands ...
Knowledge about the functions of individual proteins on a system-wide level is crucial to fully unde...
Analysis by combined liquid chromatographic separation and mass spectrometry (LC-MS) is rapidly beco...
Various stable isotope labeling (SIL) techniques have recently emerged to improve the efficiency and...
Here I describe the history of the Stable Isotope Labeling by Amino Acids in Cell culture (SILAC) te...
Stable Isotope Labeling by Amino Acids (SILAC) is a commonly used method in quantitative proteomics....
Cellular processes such as proliferation, differentiation, and adaptation to environmental changes a...
We describe a synthesis strategy for the preparation of lysine isotopologues that differ in mass by ...
Metabolic labeling with stable isotopes is a prominent technique for comparative quantitative proteo...
We describe a protocol for multiplexed proteomic analysis using neutron-encoded (NeuCode) stable iso...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
Since its introduction in 2002 'stable isotope labeling by amino acids in cell culture' (SILAC) has ...
Modern mass spectrometry (MS)-based approaches are capable of identifying and quantifying thousands ...
Knowledge about the functions of individual proteins on a system-wide level is crucial to fully unde...
Analysis by combined liquid chromatographic separation and mass spectrometry (LC-MS) is rapidly beco...
Various stable isotope labeling (SIL) techniques have recently emerged to improve the efficiency and...
Here I describe the history of the Stable Isotope Labeling by Amino Acids in Cell culture (SILAC) te...
Stable Isotope Labeling by Amino Acids (SILAC) is a commonly used method in quantitative proteomics....
Cellular processes such as proliferation, differentiation, and adaptation to environmental changes a...
We describe a synthesis strategy for the preparation of lysine isotopologues that differ in mass by ...
Metabolic labeling with stable isotopes is a prominent technique for comparative quantitative proteo...
We describe a protocol for multiplexed proteomic analysis using neutron-encoded (NeuCode) stable iso...