%0 Journal Article %1 piechuraSILACStudyMammalian2012 %A Piechura, Heike %A Oeljeklaus, Silke %A Warscheid, Bettina %C United States %D 2012 %J Methods in molecular biology (Clifton, N.J.) %K & Acids,Animals,Cell Affinity,Electrophoresis Amino Complexes/*chemistry/isolation Culture Extracts/chemistry/isolation Gel,Humans,Isotope Labeling,Mass Line Polyacrylamide Proteins/*chemistry/isolation Spectrometry,Molecular Techniques,Cell Tumor,Chromatography Weight,Multiprotein cerevisiae purification,Cell purification,Proteolysis,Proteome/*chemistry/isolation purification,Saccharomyces purification,to_read,Trypsin/chemistry %P 201--221 %R 10.1007/978-1-61779-885-6_14 %T SILAC for the Study of Mammalian Cell Lines and Yeast Protein Complexes. %V 893 %X Through crucial advancements in quantitative mass spectrometry (MS), proteomics has evolved from taking mere "snapshots" of proteomes to thoroughly studying dynamic changes in entire proteomes and characterizing intricate protein-protein interaction or signaling networks. Thus, quantitative MS-based proteomics offers the unique potential to place proteins into their functional context and, moreover, to improve our understanding of the molecular processes involved in the development, survival, or pathology of cells and organisms. Among the vast variety of techniques developed for the accurate quantification of proteins via MS, stable isotope labeling by amino acids in cell culture (SILAC) arguably represents the most elegant method. In this chapter, we provide a detailed protocol for the establishment of SILAC for mammalian cell culture systems. In addition, to exemplify the high versatility of SILAC for addressing different biological questions, we describe the successful "pairing" of SILAC with conventional affinity purification (AP)-MS approaches allowing for accurately characterizing protein complexes.

@article{piechuraSILACStudyMammalian2012, abstract = {Through crucial advancements in quantitative mass spectrometry (MS), proteomics has evolved from taking mere "snapshots" of proteomes to thoroughly studying dynamic changes in entire proteomes and characterizing intricate protein-protein interaction or signaling networks. Thus, quantitative MS-based proteomics offers the unique potential to place proteins into their functional context and, moreover, to improve our understanding of the molecular processes involved in the development, survival, or pathology of cells and organisms. Among the vast variety of techniques developed for the accurate quantification of proteins via MS, stable isotope labeling by amino acids in cell culture (SILAC) arguably represents the most elegant method. In this chapter, we provide a detailed protocol for the establishment of SILAC for mammalian cell culture systems. In addition, to exemplify the high versatility of SILAC for addressing different biological questions, we describe the successful "pairing" of SILAC with conventional affinity purification (AP)-MS approaches allowing for accurately characterizing protein complexes.}, added-at = {2024-05-17T13:01:35.000+0200}, address = {United States}, author = {Piechura, Heike and Oeljeklaus, Silke and Warscheid, Bettina}, biburl = {https://www.bibsonomy.org/bibtex/291b6453f0230f37d64e4b52d32c3f721/warscheidlab}, doi = {10.1007/978-1-61779-885-6_14}, interhash = {68b2cf264772b4786758261bf700a766}, intrahash = {91b6453f0230f37d64e4b52d32c3f721}, issn = {1940-6029 1064-3745}, journal = {Methods in molecular biology (Clifton, N.J.)}, keywords = {& Acids,Animals,Cell Affinity,Electrophoresis Amino Complexes/*chemistry/isolation Culture Extracts/chemistry/isolation Gel,Humans,Isotope Labeling,Mass Line Polyacrylamide Proteins/*chemistry/isolation Spectrometry,Molecular Techniques,Cell Tumor,Chromatography Weight,Multiprotein cerevisiae purification,Cell purification,Proteolysis,Proteome/*chemistry/isolation purification,Saccharomyces purification,to_read,Trypsin/chemistry}, langid = {english}, pages = {201--221}, pmid = {22665303}, timestamp = {2024-05-17T13:01:35.000+0200}, title = {{{SILAC}} for the Study of Mammalian Cell Lines and Yeast Protein Complexes.}, volume = 893, year = 2012 }