Abstract
The biological activity of a protein is regulated at many levels ranging from control of transcription and translation to post-translational modifications (PTM). Proteolytic processing is an irreversible PTM generating novel isoforms of a mature protein termed proteoforms. Proteoform dynamics is a major focus of current proteome research, since it has been associated with many pathological conditions. Mass-spectrometry (MS)-based proteomics and PTM-specific enrichment workflows have become the methods of choice to study proteoforms in vitro and in vivo. Here, we give an overview of currently available MS-based degradomics methods and outline how they can be optimally applied to study protease cleavage events. We discuss the advantages and disadvantages of selected approaches and describe state-of-the-art improvements in degradomics technologies. By introducing the concept of combinatorial degradomics, a combination of global discovery degradomics and highly sensitive targeted degradomics, we demonstrate how MS-based degradomics further evolves as a powerful tool in biomedical protease research.
Original language | English |
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Article number | 140392 |
Journal | Biochimica et Biophysica Acta - Proteins and Proteomics |
Volume | 1868 |
Issue number | 6 |
Number of pages | 8 |
ISSN | 1570-9639 |
DOIs | |
Publication status | Published - 2020 |
Keywords
- Protease
- Mass spectromety
- Proteomics
- Degradomics
- Targeted degradomics
- Combinational degradomics