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Continuous Enzymatic Assay for Histone Lysine Methyltransferases
Author(s) -
Philipp Rathert,
Xiaodong Cheng,
Albert Jeltsch
Publication year - 2007
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000112623
Subject(s) - methyltransferase , neurospora crassa , lysine , methylation , histone methyltransferase , enzyme , biochemistry , peptide , histone , chemistry , histone h3 , streptavidin , biology , chromatography , biotin , microbiology and biotechnology , amino acid , gene , mutant
We describe a continuous peptide methylation assay using the Neurospora crassa Dim-5 histone H3 lysine 9 (H3K9) methyltransferase as a model system. The assay uses streptavidin FlashPlates coated with target peptide. Since no washing and pipeting steps were required after the addition of the enzyme/S-adenosyl-L-methionine (AdoMet) mixture to the microplate, a continuous readout of the reaction progress was possible. We show that this assay is highly reproducible (with errors in the order of +/- 3%). The continuous assay is well suited for the simultaneous analysis of up to 384 samples, thus allowing for a rapid screening of methylation rates of different substrates under different conditions or in the presence of inhibitors.

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