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A facile method to synthesize histones with posttranslational modification mimics
Authors:Wang Zhiyong U  Wang Yane-Shih  Pai Pei-Jing  Russell William K  Russell David H  Liu Wenshe R
Affiliation:Department of Chemistry, Texas A&M University , College Station, Texas 77843, United States.
Abstract:Using an evolved pyrrolysyl-tRNA synthetase-tRNA(Pyl) pair, a Se-alkylselenocysteine was genetically incorporated into histone H3 with a high protein expression yield. Quantitative oxidative elimination of Se-alkylselenocysteine followed by Michael addition reactions with various thiol nucleophiles generated biologically active mimics of H3 with posttranslational modifications including lysine methylation, lysine acetylation, and serine phosphorylation.
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