Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins in vivo for mass spectrometric quantification. Full incorporation of isotopically heavy amino acids facilitates accurate quantification of proteins from different cultures, yet analysis methods for determination of incorporation are cumbersome and time-consuming. We present QTIPS, Quantification by Total Identified Peptides for SILAC, a straightforward, accurate method to determine the level of heavy amino acid incorporation throughout a population of peptides detected by mass spectrometry. Using QTIPS, we show that the incorporation of heavy amino acids in baker's yeast is unaffected by the use of prototrophic strains, indicating that auxotro...
Stable isotope labelling by amino acids in cell culture (SILAC) in conjunction with mass spectrometr...
This paper describes an algorithm to assist in relative quantitation of peptide post-translational m...
Recent advances in mass spectrometry have enabled proteome-wide analyses of cellular protein turnove...
Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins i...
Stable isotope labeling by amino acids in cell culture (SILAC) has become a popular labeling strateg...
Knowledge about the functions of individual proteins on a system-wide level is crucial to fully unde...
Stable isotope labeling with amino acids in cell culture (SILAC) was to use isotopic essential amino...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
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...
Quantification in proteomics largely relies on the incorporation of stable isotopes, with protocols ...
Stable isotope labeling is widely used to encode and quantify proteins in mass-spectrometry-based pr...
AbstractMethodological limitations have hampered the use of heavy water (2H2O), a convenient, univer...
ABSTRACT: The ability to acquire highly accurate quantitative data is an increasingly important part...
An approach to proteomic analysis that combines bioorthogonal noncanonical amino acid tagging (BONCA...
Stable isotope labelling by amino acids in cell culture (SILAC) in conjunction with mass spectrometr...
This paper describes an algorithm to assist in relative quantitation of peptide post-translational m...
Recent advances in mass spectrometry have enabled proteome-wide analyses of cellular protein turnove...
Stable incorporation of labeled amino acids in cell culture is a simple approach to label proteins i...
Stable isotope labeling by amino acids in cell culture (SILAC) has become a popular labeling strateg...
Knowledge about the functions of individual proteins on a system-wide level is crucial to fully unde...
Stable isotope labeling with amino acids in cell culture (SILAC) was to use isotopic essential amino...
Shotgun proteomics combined with stable isotope labeling by amino acids in cell culture (SILAC) is a...
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...
Quantification in proteomics largely relies on the incorporation of stable isotopes, with protocols ...
Stable isotope labeling is widely used to encode and quantify proteins in mass-spectrometry-based pr...
AbstractMethodological limitations have hampered the use of heavy water (2H2O), a convenient, univer...
ABSTRACT: The ability to acquire highly accurate quantitative data is an increasingly important part...
An approach to proteomic analysis that combines bioorthogonal noncanonical amino acid tagging (BONCA...
Stable isotope labelling by amino acids in cell culture (SILAC) in conjunction with mass spectrometr...
This paper describes an algorithm to assist in relative quantitation of peptide post-translational m...
Recent advances in mass spectrometry have enabled proteome-wide analyses of cellular protein turnove...