Construction, Growth, and Harvesting of Fission Yeast Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) Strains
Author(s) -
André Koch,
Claudia C. Bicho,
Weronika E. Borek,
Alejandro Carpy,
Boris Maček,
Silke Hauf,
Kenneth E. Sawin
Publication year - 2017
Publication title -
cold spring harbor protocols
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.674
H-Index - 51
eISSN - 1940-3402
pISSN - 1559-6095
DOI - 10.1101/pdb.prot091678
Subject(s) - stable isotope labeling by amino acids in cell culture , lysine , schizosaccharomyces pombe , yeast , amino acid , biochemistry , chemistry , proteome , biology , proteomics , saccharomyces cerevisiae , gene
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.
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