Lysine Acetylation Targets Protein Complexes and Co-Regulates Major Cellular Functions
Novo Nordisk Foundation · Max Planck Institute of Biochemistry
Abstract
Lysine acetylation is a reversible posttranslational modification of proteins and plays a key role in regulating gene expression. Technological limitations have so far prevented a global analysis of lysine acetylation's cellular roles. We used high-resolution mass spectrometry to identify 3600 lysine acetylation sites on 1750 proteins and quantified acetylation changes in response to the deacetylase inhibitors suberoylanilide hydroxamic acid and MS-275. Lysine acetylation preferentially targets large macromolecular complexes involved in diverse cellular processes, such as chromatin remodeling, cell cycle, splicing, nuclear transport, and actin nucleation. Acetylation impaired phosphorylation-dependent…
Citation impact
- FWCI
- 110.32
- Percentile
- 100%
- References
- 66
Authors
8- CCChunaram Choudhary
Novo Nordisk Foundation, Max Planck Institute of Biochemistry
- CKChanchal Kumar
Max Planck Institute of Biochemistry
- FGFlorian Gnad
Max Planck Institute of Biochemistry
- MLMichael L. Nielsen
Novo Nordisk Foundation, Max Planck Institute of Biochemistry
- MRMichael Rehman
Max Planck Institute of Biochemistry
Topics & keywords
- Acetylation
- Lysine
- Proteome
- Chemistry
- Biochemistry
- Phosphorylation
- Posttranslational modification
- Ubiquitin
- Good health and well-being