This paper describes an algorithm to assist in relative quantitation of peptide post-translational modifications using stable isotope labeling by amino acids in cell culture (SILAC). The described algorithm first determines the normalization factor and then calculates SILAC ratios for a list of target peptide masses using precursor ion abundances. Four yeast histone mutants were used to demonstrate the effectiveness of this approach for quantitation of peptide post-translational modifications changes. The details of the algorithm’s approach for normalization and peptide ratio calculation are described. The examples demonstrate the robustness of the approach as well as its utility to rapidly determine changes in peptide post-translational mo...
The active reprograming of cellular metabolism is a primary driver of oncogenesis and a hallmark of ...
Stable isotope labeling is widely used to encode and quantify proteins in mass-spectrometry-based pr...
Precise quantification is a major issue in contemporary proteomics. Both stable-isotope-labeling and...
This paper describes an algorithm to assist in relative quantitation of peptide post-translational m...
Since its introduction in 2002 'stable isotope labeling by amino acids in cell culture' (SILAC) has ...
Stable isotope labeling by amino acids in cell culture (SILAC) has become a popular labeling strateg...
Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins i...
Super-stable isotope labeling by amino acids in cell culture (Super-SILAC) enables the sensitive and...
Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) along with other relative quantitatio...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
In comparative proteomic studies, it is important to know the variability associated with sample pre...
Mass spectrometry-based quantitative proteomics can identify and quantify thousands of proteins in c...
Metabolic labeling techniques have recently become popular tools for the quantitative profiling of p...
Various stable isotope labeling (SIL) techniques have recently emerged to improve the efficiency and...
Metabolic stable isotope labeling is increasingly employed for accurate protein (and metabolite) qua...
The active reprograming of cellular metabolism is a primary driver of oncogenesis and a hallmark of ...
Stable isotope labeling is widely used to encode and quantify proteins in mass-spectrometry-based pr...
Precise quantification is a major issue in contemporary proteomics. Both stable-isotope-labeling and...
This paper describes an algorithm to assist in relative quantitation of peptide post-translational m...
Since its introduction in 2002 'stable isotope labeling by amino acids in cell culture' (SILAC) has ...
Stable isotope labeling by amino acids in cell culture (SILAC) has become a popular labeling strateg...
Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins i...
Super-stable isotope labeling by amino acids in cell culture (Super-SILAC) enables the sensitive and...
Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) along with other relative quantitatio...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
In comparative proteomic studies, it is important to know the variability associated with sample pre...
Mass spectrometry-based quantitative proteomics can identify and quantify thousands of proteins in c...
Metabolic labeling techniques have recently become popular tools for the quantitative profiling of p...
Various stable isotope labeling (SIL) techniques have recently emerged to improve the efficiency and...
Metabolic stable isotope labeling is increasingly employed for accurate protein (and metabolite) qua...
The active reprograming of cellular metabolism is a primary driver of oncogenesis and a hallmark of ...
Stable isotope labeling is widely used to encode and quantify proteins in mass-spectrometry-based pr...
Precise quantification is a major issue in contemporary proteomics. Both stable-isotope-labeling and...