Skip to main content

Protein lipoylation: an evolutionarily conserved metabolic regulator of health and disease.

Author(s): Rowland, Elizabeth A; Snowden, Caroline K; Cristea, Ileana M

Download
To refer to this page use: http://arks.princeton.edu/ark:/88435/pr1db7j
Abstract: Lipoylation is a rare, but highly conserved lysine posttranslational modification. To date, it is known to occur on only four multimeric metabolic enzymes in mammals, yet these proteins are staples in the core metabolic landscape. The dysregulation of these mitochondrial proteins is linked to a range of human metabolic disorders. Perhaps most striking is that lipoylation itself, the proteins that add or remove the modification, as well as the proteins it decorates are all evolutionarily conserved from bacteria to humans, highlighting the importance of this essential cofactor. Here, we discuss the biological significance of protein lipoylation, the importance of understanding its regulation in health and disease states, and the advances in mass spectrometry-based proteomic technologies that can aid these studies.
Publication Date: Feb-2018
Citation: Rowland, Elizabeth A, Snowden, Caroline K, Cristea, Ileana M. (2018). Protein lipoylation: an evolutionarily conserved metabolic regulator of health and disease.. Current opinion in chemical biology, 42 (76 - 85. doi:10.1016/j.cbpa.2017.11.003
DOI: doi:10.1016/j.cbpa.2017.11.003
ISSN: 1367-5931
EISSN: 1879-0402
Pages: 1 - 16
Language: eng
Type of Material: Journal Article
Journal/Proceeding Title: Current opinion in chemical biology
Version: Author's manuscript



Items in OAR@Princeton are protected by copyright, with all rights reserved, unless otherwise indicated.