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Chemical synthesis of histone H2A with methylation at Gln104

Chemical synthesis of histone H2A with methylation at Gln104
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摘要 Histone H2 A methylation at Gln104(H2AQ104Me) is a new type of histone post-translational modification(PTM) discovered recently. This modification has been found to have significant influence on gene transcription. However, the structural and functional consequence of glutamine methylation on nucleosome remains to be further elucidated. Obtaining of histones with site-specific methylation at glutamine residues might facilitate the studies towards a better understanding of this new PTM. In the present work, total chemical synthesis of H2AQ104 Me was carried out through use of the hydrazide-based native chemical ligation. Synthetic histone H2AQ104 Me could be successfully incorporated into nucleosomes in vitro and showed a negative influence on the nucleosome stability. Histone H2A methylation at Glnl04 (H2AQ104Me) is a new type of histone post-translational modification (PTM) discovered recently. This modification has been found to have significant influence on gene transcription. However, the structural and fimctional consequence of glutamine methylation on nucleosome remains to be further elucidated. Obtaining of histones with site-specific methylation at glutamine residues might facilitate the studies towards a better understanding of this new PTM. In the present work, total chemical synthesis of H2AQ 104Me was carried out through use of the hydrazide-based native chemical ligation. Synthetic histone H2AQ104Me could be successfully incorporated into nucleosomes in vitro and showed a negative influence on the nucleosome stability.
出处 《Science China Chemistry》 SCIE EI CAS CSCD 2017年第5期621-627,共7页 中国科学(化学英文版)
基金 supported by the National Basic Research Program of China(2013CB932800) the National Natural Science Foundation of China(21532004,21225207,81621002)
关键词 protein chemical synthesis glutamine methylation histone H2A thermal stability protein chemical synthesis, glutamine methylation, histone H2A, thermal stability

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