Neurodegenerative diseases are incurable, heterogeneous, and age-dependent disorders that challenge modern medicine. A deeper understanding of the pathogenesis underlying neuro-degenerative diseases is necessary to solve the unmet need for new diagnostic biomarkers and dis-ease-modifying therapy and reduce these diseases’ burden. Specifically, post-translational modifications (PTMs) play a significant role in neurodegeneration. Due to its proximity to the brain paren-chyma, cerebrospinal fluid (CSF) has long been used as an indirect way to measure changes in the brain. Mass spectrometry (MS) analysis in neurodegenerative diseases focusing on PTMs and in the context of biomarker discovery has improved and opened venues for analyzing more complex matrices such as brain tissue and blood. Notably, phosphorylated tau protein, truncated α-synuclein, APP and TDP-43, and many other modifications were extensively characterized by MS. Great potential is underlying specific pathological PTM-signatures for clinical application. This review fo-cuses on PTM-modified proteins involved in neurodegenerative diseases and highlights the most important and recent breakthroughs in MS-based biomarker discovery.
CITATION STYLE
Azevedo, R., Jacquemin, C., Villain, N., Fenaille, F., Lamari, F., & Becher, F. (2022, April 1). Mass Spectrometry for Neurobiomarker Discovery: The Relevance of Post-Translational Modifications. Cells. MDPI. https://doi.org/10.3390/cells11081279
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