Author/Authors :
Su، نويسنده , , Xiaodan and Jacob، نويسنده , , Naduparambil K. and Amunugama، نويسنده , , Ravindra and Lucas، نويسنده , , David M. and Knapp، نويسنده , , Amy R. and Ren، نويسنده , , Chen and Davis، نويسنده , , Melanie E. and Marcucci، نويسنده , , Guido and Parthun، نويسنده , , Mark R. and Byrd، نويسنده , , John C. and Fishel، نويسنده , , Richard and Freitas، نويسنده , , Michael A.، نويسنده ,
Abstract :
Here we describe the use of reverse-phase liquid chromatography mass spectrometry (RPLC–MS) to simultaneously characterize variants and post-translationally modified isoforms for each histone. The analysis of intact proteins significantly reduces the time of sample preparation and simplifies data interpretation. LC–MS analysis and peptide mass mapping have previously been applied to identify histone proteins and to characterize their post-translational modifications. However, these studies provided limited characterization of both linker histones and core histones. The current LC–MS analysis allows for the simultaneous observation of all histone PTMs and variants (both replacement and bulk histones) without further enrichment, which will be valuable in comparative studies. Protein identities were verified by the analysis of histone H2A species using RPLC fractionation, AU–PAGE separation and nano-LC–MS/MS.
Keywords :
histone , RPLC–MS , post-translational modification , AU–PAGE , Nano-LC–MS/MS
