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 |
|---|---|
| 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
Fingerprint
Dive into the research topics of 'Genetic Incorporation of Nε-Formyllysine, a New Histone Post-translational Modification'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver