Nature CommunicationsSystems BiologyPeer-reviewed journal article
Expanding the Landscape of Aging via Orbitrap Astral Mass Spectrometry and Tandem Mass Tag (TMT) Integration
Gregory R. KeeleiD, Yue DouiD, Seth P. Kodikara, Erin D. JefferyiD, Dina L. BaiiD, Erik Hultenius, Zichen Gao, João A. PauloiD, Steven P. GygiiD, Xiao Yan Tian, Tian ZhangiD
- Citations
- 13
- FWCI
- 3.29
- Field percentile
- top 6%
Abstract
Aging results in a progressive decline in physiological function due to the deterioration of essential biological processes, such as transcription and RNA splicing, ultimately increasing mortality risk. Although proteomics is emerging as a powerful tool for elucidating the molecular mechanisms of aging, existing studies are constrained by limited proteome coverage and only observe a narrow range of lifespan. To overcome these limitations, we integrated the Orbitrap Astral Mass Spectrometer with the multiplex tandem mass tag (TMT) technology to profile the proteomes of three brain tissues (cortex, hippocampus, striatum) and kidney in the C57BL/6JN mouse model, achieving quantification of 8,954 to 9,376 proteins per tissue (cumulatively 12,749 across all tissues). Our sample population represents balanced sampling across both sexes and three age groups (3, 12, and 20 months), comprising young adulthood to early late life (approximately 20-60 years of age for human lifespan). To enhance quantitative accuracy, we developed a peptide filtering strategy based on resolution and signal-to-noise thresholds. Our analysis uncovered distinct tissue-specific patterns of protein abundance, with age and sex differences in the kidney, while brain tissues exhibit notable age changes and limited sex differences. In addition, we identified both proteomic changes that are linear with age (i.e., continuous) and that have a non-linear pattern (i.e., non-continuous), revealing complex protein dynamics over the adult lifespan. Integrating our findings with early developmental proteomic data from brain tissues highlighted further divergent age-related trajectories, particularly in synaptic proteins. This study not only provides a robust data analysis workflow for TMT datasets generated using the Orbitrap Astral mass spectrometer but also expands the proteomic landscape of aging, capturing proteins with age and sex effects with unprecedented depth.
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Domain-specific proteome remodeling defines mouse myelin aging
Yarden Freund, Michael Schoof, … Tal Iram·bioRxiv·Jul 9, 2026
- Proteomic clocks reveal organ-specific signatures of aging in mice
Sean Lim, Andrew M. Pickering·bioRxiv·Oct 29, 2026
- Global and tissue-specific aging effects on murine proteomes
Gregory R. Keele, Jigang Zhang, … Devin K. Schweppe·Cell ReportsPeer-reviewed·Jul 1, 2023
- Proteomic characterization of aging-driven changes in the mouse brain by co-expression network analysis
Kazuya Tsumagari, Yoshiaki Sato, … Junro Kuromitsu·Scientific ReportsPeer-reviewed·Oct 24, 2023
- Longitudinal dynamics of organ-specific proteomic aging clocks over a decade of midlife
Robbe E. Neirynck, Julio A. Chirinos, … Tim De Meyer·bioRxiv·Feb 18, 2026
- Network analysis of mouse brain proteomes resolves molecular and cellular endophenotypes of aging and Aβ pathology
Sruti Rayaprolu, Sneha Malepati, … Srikant Rangaraju·bioRxiv·Nov 6, 2026