Methionine Sulfoxide Speciation in Mouse Hippocampus Revealed by Global Proteomics Exhibits Age- and Alzheimer's Disease-Dependent Changes Targeted to Mitochondrial and Glycolytic Pathways

• Published in: International journal of molecular sciences Vol. 25; no. 12; p. 6516
• Main Authors: Lopes, Filipa Blasco Tavares Pereira, Schlatzer, Daniela, Li, Mengzhen, Yilmaz, Serhan, Wang, Rihua, Qi, Xin, Ayati, Marzieh, Koyutürk, Mehmet, Chance, Mark R
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.06.2024; MDPI
• Subjects: 5XFAD; Age; Aging; Aging - metabolism; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's disease; Amino acids; Animals; Brain; Disease Models, Animal; Diseases; Enzymes; Exhibitions; Female; Glycolysis; Hippocampus - metabolism; Kinases; Male; Metabolism; Methionine - analogs & derivatives; Methionine - metabolism; methionine oxidation; Mice; Mice, Inbred C57BL; Mitochondria - metabolism; MSox; Oxidation; Oxidation-Reduction; Pathology; Peptides; Physiological aspects; Proteins; Proteome - metabolism; Proteomics; Proteomics - methods; Reactive Oxygen Species - metabolism; ROS; Scientific equipment and supplies industry; United States; United States; methionine oxidation; Alzheimer’s disease; proteomics; 5XFAD; ROS; mass spectrometry; MSox
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25126516

Methionine oxidation to the sulfoxide form (MS ) is a poorly understood post-translational modification of proteins associated with non-specific chemical oxidation from reactive oxygen species (ROS), whose chemistries are linked to various disease pathologies, including neurodegeneration. Emerging evidence shows MS site occupancy is, in some cases, under enzymatic regulatory control, mediating cellular signaling, including phosphorylation and/or calcium signaling, and raising questions as to the speciation and functional nature of MS across the proteome. The 5XFAD lineage of the C57BL/6 mouse has well-defined Alzheimer's and aging states. Using this model, we analyzed age-, sex-, and disease-dependent MS speciation in the mouse hippocampus. In addition, we explored the chemical stability and statistical variance of oxidized peptide signals to understand the needed power for MS -based proteome studies. Our results identify mitochondrial and glycolytic pathway targets with increases in MS with age as well as neuroinflammatory targets accumulating MS with AD in proteome studies of the mouse hippocampus. Further, this paper establishes a foundation for reproducible and rigorous experimental MS -omics appropriate for novel target identification in biological discovery and for biomarker analysis in ROS and other oxidation-linked diseases.