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Here, we combined an environment friendly method for protein extraction from tissue samples with lysine-acetylated peptide immunoprecipitation and excessive-accuracy tandem mass spectrometric (MS/MS) measurements, which allowed us to generate an atlas of lysine acetylation websites in sixteen completely different rat tissues.

For further validation, we selected histone H3 lysine 27 acetylation as a result of this modification has not been previously shown to be altered in CRC 19Protein immunostaining on western blots confirmed the increased K27 acetylation at H3 (Figure three ) and immunohistochemical staining of paired CRC and corresponding regular tissue sections revealed nuclear localisation of acetylated H3 protein (Figure four ).

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