摘要
Lysine formylation is a newly discovered post-translational modification (PTM) in histones and other nuclear proteins; it has a well-recognized but poorly defined role in chromatin conformation modulation and gene expression. To date, there is no general method to site-specifically incorporate Nε-formyllysine at a defined site of a protein. Here we report the highly efficient genetic incorporation of the unnatural amino acid Nε-formyllysine into proteins produced in Escherichia coli and mammalian cells, by using an orthogonal Nε-formyllysine tRNAsynthetase/tRNACUA pair. This technique can be applied to study the role of lysine formylation in epigenetic regulation.
源语言 | 英语 |
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页(从-至) | 1440-1442 |
页数 | 3 |
期刊 | ChemBioChem |
卷 | 16 |
期 | 10 |
DOI | |
出版状态 | 已出版 - 1 7月 2015 |
已对外发布 | 是 |