Extending SILAC to Proteomics of Plant Cell Lines
Author(s) -
Wolfgang Schütz,
Niklas Hausmann,
Karsten Krug,
Rüdiger Hampp,
Boris Maček
Publication year - 2011
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.110.082016
Subject(s) - stable isotope labeling by amino acids in cell culture , biology , quantitative proteomics , proteomics , computational biology , amino acid , arabidopsis , arabidopsis thaliana , biochemistry , gene , mutant
Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) is a widespread method for metabolic labeling of cells and tissues in quantitative proteomics; however, incomplete incorporation of the label has so far restricted its wider use in plants. Here, we argue that differential labeling by two different versions of the labeled amino acids renders SILAC fully applicable to dark-grown plant cell lines. By comparing Arabidopsis thaliana cell cultures labeled with two versions of heavy Lys (Lys-4 and Lys-8), we show that this simple modification of the SILAC protocol enables similar quantitation accuracy, precision, and reproducibility as conventional SILAC in animal cells.
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