Abstract
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.
Original language | English |
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Pages (from-to) | 1440-1442 |
Number of pages | 3 |
Journal | ChemBioChem |
Volume | 16 |
Issue number | 10 |
DOIs | |
Publication status | Published - 1 Jul 2015 |
Externally published | Yes |
Keywords
- amino acids
- formyllysine
- gene technology
- histones
- post-translational modifications