Mechanisms of metabolism-coupled protein modifications
- PMID: 39775169
- PMCID: PMC12124960
- DOI: 10.1038/s41589-024-01805-z
Mechanisms of metabolism-coupled protein modifications
Abstract
Intricate coupling between metabolism and protein post-translational modifications (PTMs) has emerged as a fundamental aspect of cellular regulation. Recent studies demonstrate that protein modifications can originate from diverse metabolites, and that their regulation is closely tied to the cellular metabolic state. Here we explore recently uncovered PTMs, including the concept of 'modification of a modification', as well as associated feedback and feedforward regulatory mechanisms, in which modified proteins impact not only related metabolic pathways but also other signaling cascades affecting physiology and diseases. The recently uncovered role of nucleus-localized metabolic enzymes for histone modifications additionally highlights the importance of cell-compartment-specific metabolic states. We further comment on the utility of untargeted metabolomics and proteomics for previously unrecognized PTMs and associated metabolic patterns. Together, these advances have uncovered a dynamic interplay between metabolism and PTMs, offering new perspectives for understanding metabolic regulation and developing targeted therapeutic strategies.
© 2025. Springer Nature America, Inc.
Conflict of interest statement
Competing interests: The authors declare no competing interests.
Similar articles
-
Metabolomics bridging proteomics along metabolites/oncometabolites and protein modifications: Paving the way toward integrative multiomics.J Pharm Biomed Anal. 2021 May 30;199:114031. doi: 10.1016/j.jpba.2021.114031. Epub 2021 Mar 19. J Pharm Biomed Anal. 2021. PMID: 33857836 Review.
-
Integrating Proteomics and Targeted Metabolomics to Understand Global Changes in Histone Modifications.Proteomics. 2018 Sep;18(18):e1700309. doi: 10.1002/pmic.201700309. Epub 2018 Apr 20. Proteomics. 2018. PMID: 29512899 Free PMC article. Review.
-
Chiral Posttranslational Modification to Lysine ε-Amino Groups.Acc Chem Res. 2022 May 17;55(10):1456-1466. doi: 10.1021/acs.accounts.2c00115. Epub 2022 May 2. Acc Chem Res. 2022. PMID: 35500056
-
Substrate and Functional Diversity of Protein Lysine Post-translational Modifications.Genomics Proteomics Bioinformatics. 2024 May 9;22(1):qzae019. doi: 10.1093/gpbjnl/qzae019. Genomics Proteomics Bioinformatics. 2024. PMID: 38862432 Free PMC article. Review.
-
Identification of novel post-translational modifications in linker histones from chicken erythrocytes.J Proteomics. 2015 Jan 15;113:162-77. doi: 10.1016/j.jprot.2014.10.004. Epub 2014 Oct 14. J Proteomics. 2015. PMID: 25452131
Cited by
-
The mitochondrial intermembrane space - a permanently proteostasis-challenged compartment.Biol Chem. 2025 May 27;406(5-7):263-294. doi: 10.1515/hsz-2025-0108. Print 2025 Aug 26. Biol Chem. 2025. PMID: 40435180 Review.
References
-
- Gyorgy B, Toth E, Tarcsa E, Falus A & Buzas EI Citrullination: a posttranslational modification in health and disease. Int. J. Biochem. Cell Biol 38, 1662–1677 (2006). - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous